David E. Goldgar, PhD

Languages

  • English
  • French
  • Spanish

Academic Information

  • Departments: Dermatology - Research Professor
  • Cancer Center Programs: Cancer Control & Population Sciences

Academic Office Information

  • 801-581-6465
  • Huntsman Cancer Institute
    2000 Circle of Hope
    Salt Lake City, UT 84112

Academic Bio

David Goldgar, PhD, is a research professor in the Department of Dermatology at the University of Utah and member of the Cancer Control and Population Sciences (CCPS) Program at Huntsman Cancer Institute.

Goldgar's research involves the genetic study of breast cancer and melanoma. He studies methods to clinically classify the BRCA1 and BRCA2 genes, the most well-known genes for breast cancer.

Before leaving the University of Utah to assume the position of chief of the Genetic Epidemiology Unit at the International Association of Cancer Research in Lyon, France, Goldgar was a member of the team that led to the localization, cloning, or characterization of the cancer predisposing BRCA1, BRCA2, and CDKN2A (p16) mutations. Goldgar joined the CCPS Program in 2008 upon his return to the University of Utah.

Goldgar earned a bachelor's degree and PhD from the University of Colorado, Boulder.

Education History

Type School Degree
Doctoral Training University of Colorado Medical Center
Biostatistics
Ph.D.
Graduate Training Colorado State University
Statistics
M.S.
Undergraduate University of Colorado
Mathematics
B.A.

Selected Publications

Journal Article

  1. Ferreira MA, Gamazon ER, Al-Ejeh F, Aittomaki K, Andrulis IL, Anton-Culver H, Arason A, Arndt V, Aronson KJ, Arun BK, Asseryanis E, Azzollini J, Balmana J, Barnes DR, Barrowdale D, Beckmann MW, Behrens S, Benitez J, Bermisheva M, Bialkowska K, Blomqvist C, Bogdanova NV, Bojesen SE, Bolla MK, Borg A, Brauch H, Brenner H, Broeks A, Burwinkel B, Caldes T, Caligo MA, Campa D, Campbell I, Canzian F, Carter J, Carter BD, Castelao JE, Chang-Claude J, Chanock SJ, Christiansen H, Chung WK, Claes KBM, Clarke CL, Couch FJ, Cox A, Cross SS, Czene K, Daly MB, de la Hoya M, Dennis J, Devilee P, Diez O, Dork T, Dunning AM, Dwek M, Eccles DM, Ejlertsen B, Ellberg C, Engel C, Eriksson M, Fasching PA, Fletcher O, Flyger H, Friedman E, Frost D, Gabrielson M, Gago-Dominguez M, Ganz PA, Gapstur SM, Garber J, Garcia-Closas M, Garcia-Saenz JA, Gaudet MM, Giles GG, Glendon G, Godwin AK, Goldberg MS, Goldgar DE, Gonzalez-Neira A, Greene MH, Gronwald J, Guenel P, Haiman CA, Hall P, Hamann U, He W, Heyworth J, Hogervorst FBL, Hollestelle A, Hoover RN, Hopper JL, Hulick PJ, Humphreys K, Imyanitov EN, Isaacs C, Jakimovska M, Jakubowska A, James PA, Janavicius R, Jankowitz RC, John EM, Johnson N, Joseph V, Karlan BY, Khusnutdinova E, Kiiski JI, Ko YD, Jones ME, Konstantopoulou I, Kristensen VN, Laitman Y, Lambrechts D, Lazaro C, Leslie G, Lester J, Lesueur F, Lindstrom S, Long J, Loud JT, Lubinski J, Makalic E, Mannermaa A, Manoochehri M, Margolin S, Maurer T, Mavroudis D, McGuffog L, Meindl A, Menon U, Michailidou K, Miller A, Montagna M, Moreno F, Moserle L, Mulligan AM, Nathanson KL, Neuhausen SL, Nevanlinna H, Nevelsteen I, Nielsen FC, Nikitina-Zake L, Nussbaum RL, Offit K, Olah E, Olopade OI, Olsson H, Osorio A, Papp J, Park-Simon TW, Parsons MT, Pedersen IS, Peixoto A, Peterlongo P, Pharoah PDP, Plaseska-Karanfilska D, Poppe B, Presneau N, Radice P, Rantala J, Rennert G, Risch HA, Saloustros E, Sanden K, Sawyer EJ, Schmidt MK, Schmutzler RK, Sharma P, Shu XO, Simard J, Singer CF, Soucy P, Southey MC, Spinelli JJ, Spurdle AB, Stone J, Swerdlow AJ, Tapper WJ, Taylor JA, Teixeira MR, Terry MB, Teule A, Thomassen M, Thone K, Thull DL, Tischkowitz M, Toland AE, Torres D, Truong T, Tung N, Vachon CM, van Asperen CJ, van den Ouweland AMW, van Rensburg EJ, Vega A, Viel A, Wang Q, Wappenschmidt B, Weitzel JN, Wendt C, Winqvist R, Yang XR, Yannoukakos D, Ziogas A, Kraft P, Antoniou AC, Zheng W, Easton DF, Milne RL, Beesley J, Chenevix-Trench G (2019 Apr 15). Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer. Nat Commun, 10(1), 1741.
  2. Qian F, Wang S, Mitchell J, McGuffog L, Barrowdale D, Leslie G, Oosterwijk JC, Chung WK, Evans DG, Engel C, Kast K, Aalfs CM, Adank MA, Adlard J, Agnarsson BA, Aittomaki K, Alducci E, Andrulis IL, Arun BK, Ausems MGEM, Azzollini J, Barouk-Simonet E, Barwell J, Belotti M, Benitez J, Berger A, Borg A, Bradbury AR, Brunet J, Buys SS, Caldes T, Caligo MA, Campbell I, Caputo SM, Chiquette J, Claes KBM, Margriet Collee J, Couch FJ, Coupier I, Daly MB, Davidson R, Diez O, Domchek SM, Donaldson A, Dorfling CM, Eeles R, Feliubadalo L, Foretova L, Fowler J, Friedman E, Frost D, Ganz PA, Garber J, Garcia-Barberan V, Glendon G, Godwin AK, Gomez Garcia EB, Gronwald J, Hahnen E, Hamann U, Henderson A, Hendricks CB, Hopper JL, Hulick PJ, Imyanitov EN, Isaacs C, Izatt L, Izquierdo A, Jakubowska A, Kaczmarek K, Kang E, Karlan BY, Kets CM, Kim SW, Kim Z, Kwong A, Laitman Y, Lasset C, Hyuk Lee M, Won Lee J, Lee J, Lester J, Lesueur F, Loud JT, Lubinski J, Mebirouk N, Meijers-Heijboer HEJ, Meindl A, Miller A, Montagna M, Mooij TM, Morrison PJ, Mouret-Fourme E, Nathanson KL, Neuhausen SL, Nevanlinna H, Niederacher D, Nielsen FC, Nussbaum RL, Offit K, Olah E, Ong KR, Ottini L, Park SK, Peterlongo P, Pfeiler G, Phelan CM, Poppe B, Pradhan N, Radice P, Ramus SJ, Rantala J, Robson M, Rodriguez GC, Schmutzler RK, Hutten Selkirk CG, Shah PD, Simard J, Singer CF, Sokolowska J, Stoppa-Lyonnet D, Sutter C, Yen Tan Y, Teixeira RM, Teo SH, Terry MB, Thomassen M, Tischkowitz M, Toland AE, Tucker KM, Tung N, van Asperen CJ, van Engelen K, van Rensburg EJ, Wang-Gohrke S, Wappenschmidt B, Weitzel JN, Yannoukakos D, Greene MH, Rookus MA, Easton DF, Chenevix-Trench G, Antoniou AC, Goldgar DE, Olopade OI, Rebbeck TR, Huo D (2019 Apr 1). Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study. J Natl Cancer Inst, 111(4), 350-364.
  3. Terry MB, Liao Y, Whittemore AS, Leoce N, Buchsbaum R, Zeinomar N, Dite GS, Chung WK, Knight JA, Southey MC, Milne RL, Goldgar D, Giles GG, McLachlan SA, Friedlander ML, Weideman PC, Glendon G, Nesci S, Andrulis IL, John EM, Phillips KA, Daly MB, Buys SS, Hopper JL, MacInnis RJ (2019 Apr). 10-year performance of four models of breast cancer risk: a validation study. Lancet Oncol, 20(4), 504-517.
  4. Terry MB, Daly MB, Phillips KA, Ma X, Zeinomar N, Leoce N, Dite GS, MacInnis RJ, Chung WK, Knight JA, Southey MC, Milne RL, Goldgar D, Giles GG, Weideman PC, Glendon G, Buchsbaum R, Andrulis IL, John EM, Buys SS, Hopper JL (2019 Mar 1). Risk-Reducing Oophorectomy and Breast Cancer Risk Across the Spectrum of Familial Risk. J Natl Cancer Inst, 111(3), 331-334.
  5. Escala-Garcia M, Guo Q, Dork T, Canisius S, Keeman R, Dennis J, Beesley J, Lecarpentier J, Bolla MK, Wang Q, Abraham J, Andrulis IL, Anton-Culver H, Arndt V, Auer PL, Beckmann MW, Behrens S, Benitez J, Bermisheva M, Bernstein L, Blomqvist C, Boeckx B, Bojesen SE, Bonanni B, Borresen-Dale AL, Brauch H, Brenner H, Brentnall A, Brinton L, Broberg P, Brock IW, Brucker SY, Burwinkel B, Caldas C, Caldes T, Campa D, Canzian F, Carracedo A, Carter BD, Castelao JE, Chang-Claude J, Chanock SJ, Chenevix-Trench G, Cheng TD, Chin SF, Clarke CL, Cordina-Duverger E, Couch FJ, Cox DG, Cox A, Cross SS, Czene K, Daly MB, Devilee P, Dunn JA, Dunning AM, Durcan L, Dwek M, Earl HM, Ekici AB, Eliassen AH, Ellberg C, Engel C, Eriksson M, Evans DG, Figueroa J, Flesch-Janys D, Flyger H, Gabrielson M, Gago-Dominguez M, Galle E, Gapstur SM, Garcia-Closas M, Garcia-Saenz JA, Gaudet MM, George A, Georgoulias V, Giles GG, Glendon G, Goldgar DE, Gonzalez-Neira A, Alnaes GIG, Grip M, Guenel P, Haeberle L, Hahnen E, Haiman CA, Hakansson N, Hall P, Hamann U, Hankinson S, Harkness EF, Harrington PA, Hart SN, Hartikainen JM, Hein A, Hillemanns P, Hiller L, Holleczek B, Hollestelle A, Hooning MJ, Hoover RN, Hopper JL, Howell A, Huang G, Humphreys K, Hunter DJ, Janni W, John EM, Jones ME, Jukkola-Vuorinen A, Jung A, Kaaks R, Kabisch M, Kaczmarek K, Kerin MJ, Khan S, Khusnutdinova E, Kiiski JI, Kitahara CM, Knight JA, Ko YD, Koppert LB, Kosma VM, Kraft P, Kristensen VN, Kruger U, Kuhl T, Lambrechts D, Le Marchand L, Lee E, Lejbkowicz F, Li L, Lindblom A, Lindstrom S, Linet M, Lissowska J, Lo WY, Loibl S, Lubinski J, Lux MP, MacInnis RJ, Maierthaler M, Maishman T, Makalic E, Mannermaa A, Manoochehri M, Manoukian S, Margolin S, Martinez ME, Mavroudis D, McLean C, Meindl A, Middha P, Miller N, Milne RL, Moreno F, Mulligan AM, Mulot C, Nassir R, Neuhausen SL, Newman WT, Nielsen SF, Nordestgaard BG, Norman A, Olsson H, Orr N, Pankratz VS, Park-Simon TW, Perez JIA, Perez-Barrios C, Peterlongo P, Petridis C, Pinchev M, Prajzendanc K, Prentice R, Presneau N, Prokofieva D, Pylkas K, Rack B, Radice P, Ramachandran D, Rennert G, Rennert HS, Rhenius V, Romero A, Roylance R, Saloustros E, Sawyer EJ, Schmidt DF, Schmutzler RK, Schneeweiss A, Schoemaker MJ, Schumacher F, Schwentner L, Scott RJ, Scott C, Seynaeve C, Shah M, Simard J, Smeets A, Sohn C, Southey MC, Swerdlow AJ, Talhouk A, Tamimi RM, Tapper WJ, Teixeira MR, Tengstrom M, Terry MB, Thone K, Tollenaar RAEM, Tomlinson I, Torres D, Truong T, Turman C, Turnbull C, Ulmer HU, Untch M, Vachon C, van Asperen CJ, van den Ouweland AMW, van Veen EM, Wendt C, Whittemore AS, Willett W, Winqvist R, Wolk A, Yang XR, Zhang Y, Easton DF, Fasching PA, Nevanlinna H, Eccles DM, Pharoah PDP, Schmidt MK (2019 Mar). Genome-wide association study of germline variants and breast cancer-specific mortality. Br J Cancer, 120(6), 647-657.
  6. Jiang X, Finucane HK, Schumacher FR, Schmit SL, Tyrer JP, Han Y, Michailidou K, Lesseur C, Kuchenbaecker KB, Dennis J, Conti DV, Casey G, Gaudet MM, Huyghe JR, Albanes D, Aldrich MC, Andrew AS, Andrulis IL, Anton-Culver H, Antoniou AC, Antonenkova NN, Arnold SM, Aronson KJ, Arun BK, Bandera EV, Barkardottir RB, Barnes DR, Batra J, Beckmann MW, Benitez J, Benlloch S, Berchuck A, Berndt SI, Bickeboller H, Bien SA, Blomqvist C, Boccia S, Bogdanova NV, Bojesen SE, Bolla MK, Brauch H, Brenner H, Brenton JD, Brook MN, Brunet J, Brunnstrom H, Buchanan DD, Burwinkel B, Butzow R, Cadoni G, Caldes T, Caligo MA, Campbell I, Campbell PT, Cancel-Tassin G, Cannon-Albright L, Campa D, Caporaso N, Carvalho AL, Chan AT, Chang-Claude J, Chanock SJ, Chen C, Christiani DC, Claes KBM, Claessens F, Clements J, Collee JM, Correa MC, Couch FJ, Cox A, Cunningham JM, Cybulski C, Czene K, Daly MB, deFazio A, Devilee P, Diez O, Gago-Dominguez M, Donovan JL, Dork T, Duell EJ, Dunning AM, Dwek M, Eccles DM, Edlund CK, Edwards DRV, Ellberg C, Evans DG, Fasching PA, Ferris RL, Liloglou T, Figueiredo JC, Fletcher O, Fortner RT, Fostira F, Franceschi S, Friedman E, Gallinger SJ, Ganz PA, Garber J, Garcia-Saenz JA, Gayther SA, Giles GG, Godwin AK, Goldberg MS, Goldgar DE, Goode EL, Goodman MT, Goodman G, Grankvist K, Greene MH, Gronberg H, Gronwald J, Guenel P, Hakansson N, Hall P, Hamann U, Hamdy FC, Hamilton RJ, Hampe J, Haugen A, Heitz F, Herrero R, Hillemanns P, Hoffmeister M, Hogdall E, Hong YC, Hopper JL, Houlston R, Hulick PJ, Hunter DJ, Huntsman DG, Idos G, Imyanitov EN, Ingles SA, Isaacs C, Jakubowska A, James P, Jenkins MA, Johansson M, Johansson M, John EM, Joshi AD, Kaneva R, Karlan BY, Kelemen LE, Kuhl T, Khaw KT, Khusnutdinova E, Kibel AS, Kiemeney LA, Kim J, Kjaer SK, Knight JA, Kogevinas M, Kote-Jarai Z, Koutros S, Kristensen VN, Kupryjanczyk J, Lacko M, Lam S, Lambrechts D, Landi MT, Lazarus P, Le ND, Lee E, Lejbkowicz F, Lenz HJ, Leslie G, Lessel D, Lester J, Levine DA, Li L, Li CI, Lindblom A, Lindor NM, Liu G, Loupakis F, Lubinski J, Maehle L, Maier C, Mannermaa A, Marchand LL, Margolin S, May T, McGuffog L, Meindl A, Middha P, Miller A, Milne RL, MacInnis RJ, Modugno F, Montagna M, Moreno V, Moysich KB, Mucci L, Muir K, Mulligan AM, Nathanson KL, Neal DE, Ness AR, Neuhausen SL, Nevanlinna H, Newcomb PA, Newcomb LF, Nielsen FC, Nikitina-Zake L, Nordestgaard BG, Nussbaum RL, Offit K, Olah E, Olama AAA, Olopade OI, Olshan AF, Olsson H, Osorio A, Pandha H, Park JY, Pashayan N, Parsons MT, Pejovic T, Penney KL, Peters WHM, Phelan CM, Phipps AI, Plaseska-Karanfilska D, Pring M, Prokofyeva D, Radice P, Stefansson K, Ramus SJ, Raskin L, Rennert G, Rennert HS, van Rensburg EJ, Riggan MJ, Risch HA, Risch A, Roobol MJ, Rosenstein BS, Rossing MA, De Ruyck K, Saloustros E, Sandler DP, Sawyer EJ, Schabath MB, Schleutker J, Schmidt MK, Setiawan VW, Shen H, Siegel EM, Sieh W, Singer CF, Slattery ML, Sorensen KD, Southey MC, Spurdle AB, Stanford JL, Stevens VL, Stintzing S, Stone J, Sundfeldt K, Sutphen R, Swerdlow AJ, Tajara EH, Tangen CM, Tardon A, Taylor JA, Teare MD, Teixeira MR, Terry MB, Terry KL, Thibodeau SN, Thomassen M, Bjorge L, Tischkowitz M, Toland AE, Torres D, Townsend PA, Travis RC, Tung N, Tworoger SS, Ulrich CM, Usmani N, Vachon CM, Van Nieuwenhuysen E, Vega A, Aguado-Barrera ME, Wang Q, Webb PM, Weinberg CR, Weinstein S, Weissler MC, Weitzel JN, West CML, White E, Whittemore AS, Wichmann HE, Wiklund F, Winqvist R, Wolk A, Woll P, Woods M, Wu AH, Wu X, Yannoukakos D, Zheng W, Zienolddiny S, Ziogas A, Zorn KK, Lane JM, Saxena R, Thomas D, Hung RJ, Diergaarde B, McKay J, Peters U, Hsu L, Garcia-Closas M, Eeles RA, Chenevix-Trench G, Brennan PJ, Haiman CA, Simard J, Easton DF, Gruber SB, Pharoah PDP, Price AL, Pasaniuc B, Amos CI, Kraft P, Lindstrom S (2019 Jan 25). Shared heritability and functional enrichment across six solid cancers. Nat Commun, 10(1), 431.
  7. Mavaddat N, Michailidou K, Dennis J, Lush M, Fachal L, Lee A, Tyrer JP, Chen TH, Wang Q, Bolla MK, Yang X, Adank MA, Ahearn T, Aittomaki K, Allen J, Andrulis IL, Anton-Culver H, Antonenkova NN, Arndt V, Aronson KJ, Auer PL, Auvinen P, Barrdahl M, Beane Freeman LE, Beckmann MW, Behrens S, Benitez J, Bermisheva M, Bernstein L, Blomqvist C, Bogdanova NV, Bojesen SE, Bonanni B, Borresen-Dale AL, Brauch H, Bremer M, Brenner H, Brentnall A, Brock IW, Brooks-Wilson A, Brucker SY, Bruning T, Burwinkel B, Campa D, Carter BD, Castelao JE, Chanock SJ, Chlebowski R, Christiansen H, Clarke CL, Collee JM, Cordina-Duverger E, Cornelissen S, Couch FJ, Cox A, Cross SS, Czene K, Daly MB, Devilee P, Dork T, Dos-Santos-Silva I, Dumont M, Durcan L, Dwek M, Eccles DM, Ekici AB, Eliassen AH, Ellberg C, Engel C, Eriksson M, Evans DG, Fasching PA, Figueroa J, Fletcher O, Flyger H, Forsti A, Fritschi L, Gabrielson M, Gago-Dominguez M, Gapstur SM, Garcia-Saenz JA, Gaudet MM, Georgoulias V, Giles GG, Gilyazova IR, Glendon G, Goldberg MS, Goldgar DE, Gonzalez-Neira A, Grenaker Alnaes GI, Grip M, Gronwald J, Grundy A, Guenel P, Haeberle L, Hahnen E, Haiman CA, Hakansson N, Hamann U, Hankinson SE, Harkness EF, Hart SN, He W, Hein A, Heyworth J, Hillemanns P, Hollestelle A, Hooning MJ, Hoover RN, Hopper JL, Howell A, Huang G, Humphreys K, Hunter DJ, Jakimovska M, Jakubowska A, Janni W, John EM, Johnson N, Jones ME, Jukkola-Vuorinen A, Jung A, Kaaks R, Kaczmarek K, Kataja V, Keeman R, Kerin MJ, Khusnutdinova E, Kiiski JI, Knight JA, Ko YD, Kosma VM, Koutros S, Kristensen VN, Kruger U, Kuhl T, Lambrechts D, Le Marchand L, Lee E, Lejbkowicz F, Lilyquist J, Lindblom A, Lindstrom S, Lissowska J, Lo WY, Loibl S, Long J, Lubinski J, Lux MP, MacInnis RJ, Maishman T, Makalic E, Maleva Kostovska I, Mannermaa A, Manoukian S, Margolin S, Martens JWM, Martinez ME, Mavroudis D, McLean C, Meindl A, Menon U, Middha P, Miller N, Moreno F, Mulligan AM, Mulot C, Munoz-Garzon VM, Neuhausen SL, Nevanlinna H, Neven P, Newman WG, Nielsen SF, Nordestgaard BG, Norman A, Offit K, Olson JE, Olsson H, Orr N, Pankratz VS, Park-Simon TW, Perez JIA, Perez-Barrios C, Peterlongo P, Peto J, Pinchev M, Plaseska-Karanfilska D, Polley EC, Prentice R, Presneau N, Prokofyeva D, Purrington K, Pylkas K, Rack B, Radice P, Rau-Murthy R, Rennert G, Rennert HS, Rhenius V, Robson M, Romero A, Ruddy KJ, Ruebner M, Saloustros E, Sandler DP, Sawyer EJ, Schmidt DF, Schmutzler RK, Schneeweiss A, Schoemaker MJ, Schumacher F, Schurmann P, Schwentner L, Scott C, Scott RJ, Seynaeve C, Shah M, Sherman ME, Shrubsole MJ, Shu XO, Slager S, Smeets A, Sohn C, Soucy P, Southey MC, Spinelli JJ, Stegmaier C, Stone J, Swerdlow AJ, Tamimi RM, Tapper WJ, Taylor JA, Terry MB, Thone K, Tollenaar RAEM, Tomlinson I, Truong T, Tzardi M, Ulmer HU, Untch M, Vachon CM, van Veen EM, Vijai J, Weinberg CR, Wendt C, Whittemore AS, Wildiers H, Willett W, Winqvist R, Wolk A, Yang XR, Yannoukakos D, Zhang Y, Zheng W, Ziogas A, Dunning AM, Thompson DJ, Chenevix-Trench G, Chang-Claude J, Schmidt MK, Hall P, Milne RL, Pharoah PDP, Antoniou AC, Chatterjee N, Kraft P, Garcia-Closas M, Simard J, Easton DF (2019 Jan 3). Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes. Am J Hum Genet, 104(1), 21-34.
  8. Drost M, Tiersma Y, Thompson BA, Frederiksen JH, Keijzers G, Glubb D, Kathe S, Osinga J, Westers H, Pappas L, Boucher KM, Molenkamp S, Zonneveld JB, van Asperen CJ, Goldgar DE, Wallace SS, Sijmons RH, Spurdle AB, Rasmussen LJ, Greenblatt MS, de Wind N, Tavtigian SV (2018 Dec 3). A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome.LID - 10.1038/s41436-018-0372-2 [doi]. (Epub ahead of print) Genet Med.
  9. Cline MS, Liao RG, Parsons MT, Paten B, Alquaddoomi F, Antoniou A, Baxter S, Brody L, Cook-Deegan R, Coffin A, Couch FJ, Craft B, Currie R, Dlott CC, Dolman L, den Dunnen JT, Dyke SOM, Domchek SM, Easton D, Fischmann Z, Foulkes WD, Garber J, Goldgar D, Goldman MJ, Goodhand P, Harrison S, Haussler D, Kato K, Knoppers B, Markello C, Nussbaum R, Offit K, Plon SE, Rashbass J, Rehm HL, Robson M, Rubinstein WS, Stoppa-Lyonnet D, Tavtigian S, Thorogood A, Zhang C, Zimmermann M, Burn J, Chanock S, Ratsch G, Spurdle AB (2018 Dec). BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2. PLoS Genet, 14(12), e1007752.
  10. Terry MB, Liao Y, Kast K, Antoniou AC, McDonald JA, Mooij TM, Engel C, Nogues C, Buecher B, Mari V, Moretta-Serra J, Gladieff L, Luporsi E, Barrowdale D, Frost D, Henderson A, Brewer C, Evans DG, Eccles D, Cook J, Ong KR, Izatt L, Ahmed M, Morrison PJ, Dommering CJ, Oosterwijk JC, Ausems MGEM, Kriege M, Buys SS, Andrulis IL, John EM, Daly M, Friedlander M, McLachlan SA, Osorio A, Caldes T, Jakubowska A, Simard J, Singer CF, Tan Y, Olah E, Navratilova M, Foretova L, Gerdes AM, Roos-Blom MJ, Arver B, Olsson H, Schmutzler RK, Hopper JL, van Leeuwen FE, Goldgar D, Milne RL, Easton DF, Rookus MA, Andrieu N (2018 Dec). The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations. JNCI Cancer Spectr, 2(4), pky078.
  11. Lu Y, Beeghly-Fadiel A, Wu L, Guo X, Li B, Schildkraut JM, Im HK, Chen YA, Permuth JB, Reid BM, Teer JK, Moysich KB, Andrulis IL, Anton-Culver H, Arun BK, Bandera EV, Barkardottir RB, Barnes DR, Benitez J, Bjorge L, Brenton J, Butzow R, Caldes T, Caligo MA, Campbell I, Chang-Claude J, Claes KBM, Couch FJ, Cramer DW, Daly MB, deFazio A, Dennis J, Diez O, Domchek SM, Dork T, Easton DF, Eccles DM, Fasching PA, Fortner RT, Fountzilas G, Friedman E, Ganz PA, Garber J, Giles GG, Godwin AK, Goldgar DE, Goodman MT, Greene MH, Gronwald J, Hamann U, Heitz F, Hildebrandt MAT, Hogdall CK, Hollestelle A, Hulick PJ, Huntsman DG, Imyanitov EN, Isaacs C, Jakubowska A, James P, Karlan BY, Kelemen LE, Kiemeney LA, Kjaer SK, Kwong A, Le ND, Leslie G, Lesueur F, Levine DA, Mattiello A, May T, McGuffog L, McNeish IA, Merritt MA, Modugno F, Montagna M, Neuhausen SL, Nevanlinna H, Nielsen FC, Nikitina-Zake L, Nussbaum RL, Offit K, Olah E, Olopade OI, Olson SH, Olsson H, Osorio A, Park SK, Parsons MT, Peeters PHM, Pejovic T, Peterlongo P, Phelan CM, Pujana MA, Ramus SJ, Rennert G, Risch H, Rodriguez GC, Rodriguez-Antona C, Romieu I, Rookus MA, Rossing MA, Rzepecka IK, Sandler DP, Schmutzler RK, Setiawan VW, Sharma P, Sieh W, Simard J, Singer CF, Song H, Southey MC, Spurdle AB, Sutphen R, Swerdlow AJ, Teixeira MR, Teo SH, Thomassen M, Tischkowitz M, Toland AE, Trichopoulou A, Tung N, Tworoger SS, van Rensburg EJ, Vanderstichele A, Vega A, Edwards DV, Webb PM, Weitzel JN, Wentzensen N, White E, Wolk A, Wu AH, Yannoukakos D, Zorn KK, Gayther SA, Antoniou AC, Berchuck A, Goode EL, Chenevix-Trench G, Sellers TA, Pharoah PDP, Zheng W, Long J (2018 Sep 15). A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk. Cancer Res, 78(18), 5419-5430.
  12. Burke LJ, Sevcik J, Gambino G, Tudini E, Mucaki EJ, Shirley BC, Whiley P, Parsons MT, De Leeneer K, Gutierrez-Enriquez S, Santamarina M, Caputo SM, Santana Dos Santos E, Soukupova J, Janatova M, Zemankova P, Lhotova K, Stolarova L, Borecka M, Moles-Fernandez A, Manoukian S, Bonanni B, Edwards SL, Blok MJ, van Overeem Hansen T, Rossing M, Diez O, Vega A, Claes KBM, Goldgar DE, Rouleau E, Radice P, Peterlongo P, Rogan PK, Caligo M, Spurdle AB, Brown MA (2018 Sep 11). BRCA1 and BRCA2 5' non-coding region variants identified in breast cancer patients alter promoter activity and protein binding.LID - 10.1002/humu.23652 [doi]. (Epub ahead of print) Hum Mutat.
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  210. Meijers-Heijboer H, van den Ouweland A, Klijn J, Wasielewski M, de Snoo A, Oldenburg R, Hollestelle A, Houben M, Crepin E, van Veghel-Plandsoen M, Elstrodt F, van Duijn C, Bartels C, Meijers C, Schutte M, McGuffog L, Thompson D, Easton D, Sodha N, Seal S, Barfoot R, Mangion J, Chang-Claude J, Eccles D, Eeles R, Evans DG, Houlston R, Murday V, Narod S, Peretz T, Peto J, Phelan C, Zhang HX, Szabo C, Devilee P, Goldgar D, Futreal PA, Nathanson KL, Weber B, Rahman N, Stratton MR (2002 May). Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet, 31(1), 55-9.
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  239. Lakhani SR, Sloane JP, Gusterson BA, Anderson TJ, Jacquemier J, van de Vijver M, Farid L, Storfer-Isser A, Smyth E, Steel CM, Haites N, Scott R, Goldgar D, Neuhausen S, Scherneck S, Ponder BAJ, Ford D, Peto J, Sobol H, Bignon Y, Streuwing J, Spurr N, Bishop DT, Devilee P, Cornelisse C, Lenoir G, Barkadottir RB, Egilsson V, Hamman U, Chang-Claude J, Weber B, Easton DF, Stratton MR (1997). Pathology of familial breast cancer: differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases. Lancet, 349, 1505-1510.
  240. Schuffenecker I, Ginet N, Goldgar D, Eng C, Chambe B, Boneu A, Houdent C, Pallo D, Schlumberger M, Thivolet C, Lenoir GM (1997 Jan). Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Le Groupe d'Etude des Tumeurs a Calcitonine. Am J Hum Genet, 60(1), 233-7.
  241. Mazoyer S, Dunning AM, Serova O, Dearden J, Puget N, Healey CS, Gayther SA, Mangion J, Stratton MR, Lynch HT, Goldgar DE, Ponder BA, Lenoir GM (1996 Nov). A polymorphic stop codon in BRCA2. Nat Genet, 14(3), 253-4.
  242. Oddoux C, Struewing JP, Clayton CM, Neuhausen S, Brody LC, Kaback M, Haas B, Norton L, Borgen P, Jhanwar S, Goldgar D, Ostrer H, Offit K (1996 Oct). The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%. Nat Genet, 14(2), 188-90.
  243. Botkin JR, Croyle RT, Smith KR, Baty BJ, Lerman C, Goldgar DE, Ward JM, Flick BJ, Nash JE (1996 Jul 03). A model protocol for evaluating the behavioral and psychosocial effects of BRCA1 testing. J Natl Cancer Inst, 88(13), 872-82.
  244. Offit K, Gilewski T, McGuire P, Schluger A, Hampel H, Brown K, Swensen J, Neuhausen S, Skolnick M, Norton L, Goldgar D (1996 Jun 15). Germline BRCA1 185delAG mutations in Jewish women with breast cancer. Lancet, 347(9016), 1643-5.
  245. Durocher F, Shattuck-Eidens D, McClure M, Labrie F, Skolnick MH, Goldgar DE, Simard J (1996 Jun). Comparison of BRCA1 polymorphisms, rare sequence variants and/or missense mutations in unaffected and breast/ovarian cancer populations. Hum Mol Genet, 5(6), 835-42.
  246. Neuhausen S, Gilewski T, Norton L, Tran T, McGuire P, Swensen J, Hampel H, Borgen P, Brown K, Skolnick M, Shattuck-Eidens D, Jhanwar S, Goldgar D, Offit K (1996 May). Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer. Nat Genet, 13(1), 126-8.
  247. Phelan CM, Rebbeck TR, Weber BL, Devilee P, Ruttledge MH, Lynch HT, Lenoir GM, Stratton MR, Easton DF, Ponder BA, Cannon-Albright L, Larsson C, Goldgar DE, Narod SA (1996 Mar). Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus. Nat Genet, 12(3), 309-11.
  248. Tavtigian SV, Simard J, Rommens J, Couch F, Shattuck-Eidens D, Neuhausen S, Merajver S, Thorlacius S, Offit K, Stoppa-Lyonnet D, Belanger C, Bell R, Berry S, Bogden R, Chen Q, Davis T, Dumont M, Frye C, Hattier T, Jammulapati S, Janecki T, Jiang P, Kehrer R, Leblanc JF, Mitchell JT, McArthur-Morrison J, Nguyen K, Peng Y, Samson C, Schroeder M, Snyder SC, Steele L, Stringfellow M, Stroup C, Swedlund B, Swense J, Teng D, Thomas A, Tran T, Tranchant M, Weaver-Feldhaus J, Wong AK, Shizuya H, Eyfjord JE, Cannon-Albright L, Tranchant M, Labrie F, Skolnick MH, Weber B, Kamb A, Goldgar DE (1996 Mar). The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds. Nat Genet, 12(3), 333-7.
  249. Neuhausen SL, Mazoyer S, Friedman L, Stratton M, Offit K, Caligo A, Tomlinson G, Cannon-Albright L, Bishop T, Kelsell D, Solomon E, Weber B, Couch F, Struewing J, Tonin P, Durocher F, Narod S, Skolnick MH, Lenoir G, Serova O, Ponder B, Stoppa-Lyonnet D, Easton D, King MC, Goldgar DE (1996 Feb). Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study. Am J Hum Genet, 58(2), 271-80.
  250. Meyer LJ, Peipkorn MW, Goldgar DE, Lewis CM, Cannon-Albright L, Zone JJ, Skolnick M (1996). The appearance of atypical melanocytic nevi: correlation between observers and with pathology. Am J Dermatopathol.
  251. Narod SA, Goldgar D, Cannon-Albright L, Weber B, Moslehi R, Ives E, Lenoir G, Lynch H (1995 Dec 20). Risk modifiers in carriers of BRCA1 mutations. Int J Cancer, 64(6), 394-8.
  252. Goldgar DE, Reilly PR (1995 Oct). A common BRCA1 mutation in the Ashkenazim. Nat Genet, 11(2), 113-4.
  253. Meyer LJ, Schmidt LA, Goldgar DE, Piepkorn MW (1995 Aug). Survival and histopathologic characteristics of human melanocytic nevi transplanted to athymic (nude) mice. Am J Dermatopathol, 17(4), 368-73.
  254. Narod SA, Ford D, Devilee P, Barkardottir RB, Lynch HT, Smith SA, Ponder BAJ, Weber BL, Garber J, Birch JM, Cornelis RS, Kelsell DP, Spurr N, Smyth E, Haites N, Sobol H, Bignon YJ, Claude-Chang J, Hamann U, Lindblom A, Borg A, Piver MS, Gallion HH, Struewing JP, Whittemore A, Tonin P, Goldgar DE, Easton DF, the Breast Cancer Linkage Consortium (1995). An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Am J Hum Genet, 56, 254-265.
  255. Shattuck-Eidens D, McClure M, Simard J, Labrie F, Narod S, Couch F, Weber B, Castilla L, Brody L, Friedman L, Ostermeyer E, Szabo C, King MC, Jhanwar S, Offit K, Norton L, Gilewski T, Lubin M, Osborne M, Black D, Boyd M, Steel M, Ingles S, Haile R, Lindblom An, Borg A, Bishop DT, Soloman E, Radice P, Spatti G, Gayther S, Ponder B, Warren W, Stratton M, Liu Q, Fujimura F, Lewis C, Skolnick MH, Goldgar DE (1995). A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene: Implications for presymptomatic testing and screening. J Am Med Assoc, 273, 535-541.
  256. Goldgar DE, Neuhausen SL, Steele L, Fields P, Ward JH, Tran T, Ngyuen K, Stratton MR, Easton DF (1995). A 45-year follow-up of kindred 107 and the search for BRCA2. J Natl Cancer Inst Monogr, (17), 15-9.
  257. Lewis CM, Goldgar DE (1995). Screening for linkage using a multipoint identity-by-descent method. Genet Epidemiol, 12(6), 777-82.
  258. Goldgar DE (1995). Analysis of familial breast cancer in genetic analysis workshop 9: summary of findings. Genet Epidemiol, 12(6), 833-6.
  259. Cannon-Albright LA, Meyer LJ, Goldgar DE, Lewis CM, McWhorter WP, Jost M, Harrison D, Anderson DE, Zone JJ, Skolnick MH (1994 Dec 01). Penetrance and expressivity of the chromosome 9p melanoma susceptibility locus (MLM). Cancer Res, 54(23), 6041-4.
  260. Goldgar DE, Easton DF, Cannon-Albright LA, Skolnick MH (1994 Nov 02). Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands. J Natl Cancer Inst, 86(21), 1600-8.
  261. Cannon-Albright LA, Goldgar DE, Neuhausen S, Gruis NA, Anderson DE, Lewis CM, Jost M, Tran TD, Nyguen K, Kamb A, et al (1994 Sep 01). Localization of the 9p melanoma susceptibility locus (MLM) to a 2-cM region between D9S736 and D9S171. Genomics, 23(1), 265-8.
  262. Cannon-Albright LA, Thomas A, Goldgar DE, Gholami K, Rowe K, Jacobsen M, McWhorter WP, Skolnick MH (1994 May 01). Familiality of cancer in Utah. Cancer Res, 54(9), 2378-85.
  263. Piepkorn MW, Barnhill RL, Cannon-Albright LA, Elder DE, Goldgar DE, Lewis CM, Maize JC, Meyer LJ, Rabkin MS, Sagebiel RW, et al (1994 May). A multiobserver, population-based analysis of histologic dysplasia in melanocytic nevi. J Am Acad Dermatol, 30(5 Pt 1), 707-14.
  264. Ford D, Easton DF, Bishop DT, Narod SA, Goldgar DE (1994 Mar 19). Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium. Lancet, 343(8899), 692-5.
  265. Goldgar DE, Fields P, Lewis CM, Tran TD, Cannon-Albright LA, Ward JH, Swensen J, Skolnick MH (1994 Feb 02). A large kindred with 17q-linked breast and ovarian cancer: genetic, phenotypic, and genealogical analysis. J Natl Cancer Inst, 86(3), 200-9.
  266. Miki Y, Swensen J, Shattuck-Eidens, D, Futreal PA, Harshman K, Tavtigian S, Liu Q, Cochran C, Bennett LM, Ding W, Bell R, Rosenthal J, Hussey C, Tran T, McClure M, Frye C, Hattier T, Phelps R, Haugen-Strano A, Katcher H, Yakumo K, Gholami Z, Shaffer D, Stone S, Bayer S, Wray C, Bogden R, Dayananth P, Ward J, Tonin P, Narod S, Bristow PK, Norris FH, Helvering L, Morrison P, Rosteck P, Lai M, Barrett JC, Lewis C, Neuhausen S, Cannon-Albright L, Goldgar D, Wiseman R, Kamb A, Skolnick MH (1994). A Strong candidate for the 17q-linked breast and ovarian cancer susceptibility gene BRCA1. Science, 266, 66-71.
  267. Simard J, Tonin P, Durocher F, Morgan K, Rommens J, Gingras S, Samson C, Leblanc J-F, Belanger C, Dion F, Liu Q, Skolnick M, Goldgar D, Shattuck-Eidens D, Labrie F, Narod SA (1994). Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families. Nat Genet, 8, 392-398.
  268. Neuhausen SL, Swensen JJ, Miki Y, Liu Q, Tavtigian S, Shatuck-Eidens D, Kamb A, Hobbs MR, Gingrich J, Shizuya H, Kim U-J, Cochran C, Futreal PA, Wiseman RW, Lynch HT, Tonin P, Narod S, Cannon-Albright L, Skolnick MH, Goldgar D (1994). A P1-based physical map of the BRCA1 region from D17S776 to D17S78. Hum Mol Genet, 3(11), 1919-1926.
  269. Stratton MR, Ford D, Neuhausen S, Seal S, Wooster R, Friedman LS, King M-C, Egilsson V, Devilee P, McMarus R, Daly PA, Smith E, Ponder BAJ, Peto J, Cannon-Albright L, Easton D, Goldgar D (1994). Familial male breast cancer is not linked to BRCA1 locus on chromosome 17q. Nat Genet, 7, 103-106.
  270. Kamb A, Shattuck-Eidens D, Eeles R, Liu Q, Gruis NA, Ding W, Hussey C, Tran T, Miki Y, Weaver-Feldhaus J, McClure M, Aitken JF, Anderson DE, BergmanW, Frants R, Goldgar DE, Green A, MacLennan R, Martin NG, Meyer LJ, Youl P, Zone JJ, Skolnick MH, Cannon-Albright LA (1994). Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus. Nat Genet, 8, 22-26.
  271. Wooster R, Neuhausen S, Mangion J, Quirk Y, Ford D, Collins N, Nguyen K, Seal S, Tran T, Averill D, Fields P, Marshall G, Narod S, Lenoir G, Lynch H, Feunteun J, Devilee P, Cornelisse CJ, Menko FH, Daly PA, Ormiston W, McManus R, Pye C, Lewis C, Cannon-Albright L, Peto J, Ponder BAJ, Skolnick MH, Easton DF, Goldgar DE, Stratton MR (1994). Localisation of a breast cancer susceptibility gene, (BRCA2), to chromosome 13q 12-13. Science, 265, 2088-2090.
  272. Piepkorn M, Cannon-Albright LA, Meyer LJ, Goldgar DE, Zone JJ, Skolnick MH (1994). Genetic predisposition to melanoma. Melanoma Letter, 12(2), 1-4.
  273. Chenevix-Trench G, Wicking C, Berkman J, Sharpe H, Hockey A, Haan E, Oley C, Ravine D, Turner A, Goldgar D, et al (1993 Sep). Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity. Am J Hum Genet, 53(3), 760-7.
  274. Goldgar DE, Cannon-Albright LA, Oliphant A, Ward JH, Linker G, Swensen J, Tran TD, Fields P, Uharriet P, Skolnick MH (1993 Apr). Chromosome 17q linkage studies of 18 Utah breast cancer kindreds. Am J Hum Genet, 52(4), 743-8.
  275. Goldgar DE, Lewis CM, Gholami K (1993). Analysis of discrete phenotypes using a multipoint identity-by-descent method: application to Alzheimer's disease. Genet Epidemiol, 10(6), 383-8.
  276. Cannon-Albright LA, Goldgar DE, Meyer LJ, Lewis CM, Anderson DE, Fountain JW, Hegi ME, Wiseman RW, Petty EM, Bale AE, et al (1992 Nov 13). Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22. Science, 258(5085), 1148-52.
  277. Goldgar DE, Oniki RS (1992 Mar). Comparison of a multipoint identity-by-descent method with parametric multipoint linkage analysis for mapping quantitative traits. Am J Hum Genet, 50(3), 598-606.
  278. Stern HJ, Saal HM, Lee JS, Fain PR, Goldgar DE, Rosenbaum KN, Barker DF (1992 Mar). Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome? J Med Genet, 29(3), 184-7.
  279. Meyer LJ, Goldgar DE, Cannon-Albright LA, Piepkorn MW, Zone JJ, Risman MB, Skolnick MH (1992). Number, size, and histopathology of nevi in Utah kindreds. Cytogenet Cell Genet, 59(2-3), 167-9.
  280. Goldgar DE, Cannon-Albright LA, Meyer LJ, Piepkorn MW, Zone JJ, Skolnick MH (1992). Inheritance of nevus number and size in melanoma/DNS kindreds. Cytogenet Cell Genet, 59(2-3), 200-2.
  281. Goldgar DE, Cannon-Albright LA, Meyer LJ, Piepkorn MW, Zone JJ, Skolnick MH (1991 Dec 04). Inheritance of nevus number and size in melanoma and dysplastic nevus syndrome kindreds. J Natl Cancer Inst, 83(23), 1726-33.
  282. Barker DF, Fain PR, Goldgar DE, Dietz-Band JN, Turco AE, Kashtan CE, Gregory MC, Tryggvason K, Skolnick MH, Atkin CL (1991 Dec). High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers. Hum Genet, 88(2), 189-94.
  283. Oliphant AR, Wright EC, Swensen J, Gruis NA, Goldgar D, Skolnick MH (1991 Sep 11). Dinucleotide repeat polymorphism at the D17S514 locus. Nucleic Acids Res, 19(17), 4794.
  284. Oliphant AR, Wright EC, Swensen J, Gruis NA, Goldgar D, Skolnick MH (1991 Sep 11). Dinucleotide repeat polymorphism at the D17S513 locus. Nucleic Acids Res, 19(17), 4794.
  285. Ahmed I, Piepkorn M, Goldgar DE, Cannon-Albright LA, Meyer LJ, Skolnick MH, Zone JJ (1991 Aug). HMB-45 staining of dysplastic melanocytic nevi in melanoma risk groups. J Cutan Pathol, 18(4), 257-60.
  286. Gallagher JC, Kable WT, Goldgar D (1991 Feb). Effect of progestin therapy on cortical and trabecular bone: comparison with estrogen. Am J Med, 90(2), 171-8.
  287. Skolnick MH, Marshall CJ, McWhorter W, Goldgar D, Cannon-Albright L, Ward JH, Eyre H (1991). Proliferative breast disease: diagnosis and implications Response. Science, 253, 915-916.
  288. Molczyk L, Thigpen LK, Eickhoff J, Goldgar D, Gallagher JC (1991). Reliability of Testing the Knee Extensors and Flexors in Healthy Adult Women Using a Cybex II Isokinetic Dynamometer. J Orthop Sports Phys Ther, 14(1), 37-41.
  289. Kable WT, Nachtigall L, Goldgar DE, Gallagher JC (1991). Effect of Estrogen and progesteron on lipids metabolism. J Reprod Med.
  290. Skolnick MH, Cannon-Albright LA, Goldgar DE, Ward JH, Marshall CJ, Schumann GB, Hogle H, McWhorter WP, Wright EC, Tran TD, et al (1990 Dec 21). Inheritance of proliferative breast disease in breast cancer kindreds. Science, 250(4988), 1715-20.
  291. Goldgar DE (1990 Dec). Multipoint analysis of human quantitative genetic variation. Am J Hum Genet, 47(6), 957-67.
  292. Gallagher JC, Goldgar D (1990 Nov 01). Treatment of postmenopausal osteoporosis with high doses of synthetic calcitriol. A randomized controlled study. Ann Intern Med, 113(9), 649-55.
  293. Cannon-Albright LA, Goldgar DE, Wright EC, Turco A, Jost M, Meyer LJ, Piepkorn M, Zone JJ, Skolnick MH (1990 May). Evidence against the reported linkage of the cutaneous melanoma-dysplastic nevus syndrome locus to chromosome Ip36. Am J Hum Genet, 46(5), 912-8.
  294. Wright EC, Goldgar DE, Fain PR, Barker DF, Skolnick MH (1990 May). A genetic map of human chromosome 17p. Genomics, 7(1), 103-9.
  295. Fain PR, Goldgar DE, Wallace MR, Collins FS, Wright E, Nguyen K, Barker DF (1989 Nov). Refined physical and genetic mapping of the NF1 region on chromosome 17. Am J Hum Genet, 45(5), 721-8.
  296. Edwards CQ, Griffen LM, Goldgar DE, Skolnick MH, Kushner JP (1989 Oct). HLA-linked hemochromatosis alleles in sporadic porphyria cutanea tarda. Gastroenterology, 97(4), 972-81.
  297. Goldgar DE, Fain PR, Kimberling WJ (1989 Aug). Chiasma-based models of multilocus recombination: increased power for exclusion mapping and gene ordering. Genomics, 5(2), 283-90.
  298. Gallagher JC, Riggs BL, Recker RR, Goldgar D (1989 Jul). The effect of calcitriol on patients with postmenopausal osteoporosis with special reference to fracture frequency. Proc Soc Exp Biol Med, 191(3), 287-92.
  299. Piepkorn M, Meyer LJ, Goldgar D, Seuchter SA, Cannon-Albright LA, Skolnick MH, Zone JJ (1989 Mar). The dysplastic melanocytic nevus: a prevalent lesion that correlates poorly with clinical phenotype. J Am Acad Dermatol, 20(3), 407-15.
  300. Goldgar DE, Green P, Parry DM, Mulvihill JJ (1989 Jan). Multipoint linkage analysis in neurofibromatosis type I: an international collaboration. Am J Hum Genet, 44(1), 6-12.
  301. Goldgar DE, Fain PR, Green P (1989). Multipoint analysis of 47 loci on chromosome 7q. Prog Clin Biol Res, 329, 23-8.
  302. Kimberling WJ, Fain PR, Kenyon JB, Goldgar D, Sujansky E, Gabow PA (1988 Oct 06). Linkage heterogeneity of autosomal dominant polycystic kidney disease. N Engl J Med, 319(14), 913-8.
  303. Watson BU, Goldgar DE (1988 Aug). Evaluation of a typology of reading disability. J Clin Exp Neuropsychol, 10(4), 432-50.
  304. Goldgar DE, Fain PR (1988 Jul). Models of multilocus recombination: nonrandomness in chiasma number and crossover positions. Am J Hum Genet, 43(1), 38-45.
  305. Edwards CQ, Griffen LM, Goldgar D, Drummond C, Skolnick MH, Kushner JP (1988 May 26). Prevalence of hemochromatosis among 11,065 presumably healthy blood donors. N Engl J Med, 318(21), 1355-62.
  306. Elbein SC, Corsetti L, Goldgar D, Skolnick M, Permutt MA (1988 May). Insulin gene in familial NIDDM. Lack of linkage in Utah Mormon pedigrees. Diabetes, 37(5), 569-76.
  307. Goldgar DE, Thompson EA (1988 Jan). Bayesian interval estimation of genetic relationships: application to paternity testing. Am J Hum Genet, 42(1), 135-42.
  308. Gallagher JC, Goldgar D, Moy A (1987 Dec). Total bone calcium in normal women: effect of age and menopause status. J Bone Miner Res, 2(6), 491-6.
  309. Fain PR, Barker DF, Goldgar DE, Wright E, Nguyen K, Carey J, Johnson J, Kivlin J, Willard H, Mathew C, et al (1987 Dec). Genetic analysis of NF1: identification of close flanking markers on chromosome 17. Genomics, 1(4), 340-5.
  310. White R, Nakamura Y, OConnell P, Leppert M, Lalouel JM, Barker D, Goldgar D, Skolnick M, Carey J, Wallis CE, et al (1987 Dec). Tightly linked markers for the neurofibromatosis type 1 gene. Genomics, 1(4), 364-7.
  311. Barker D, Wright E, Nguyen K, Cannon L, Fain P, Goldgar D, Bishop DT, Carey J, Kivlin J, Willard H, et al (1987 Sep). A genomic search for linkage of neurofibromatosis to RFLPs. J Med Genet, 24(9), 536-8.
  312. Barker D, Wright E, Nguyen K, Cannon L, Fain P, Goldgar D, Bishop DT, Carey J, Baty B, Kivlin J, et al (1987 May 29). Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17. Science, 236(4805), 1100-2.
  313. Kimberling WJ, Goldgar DE, Penno MB, Vesell ES (1987 Jan). Pharmacogenetic application of methods from population genetics. Clin Pharmacol Ther, 41(1), 3-10.
  314. Goldgar D, Osberger MJ (1986 Mar). Language and learning skills of hearing-impaired students. Factors related to academic achievement. ASHA Monogr, (23), 87-91.
  315. Watson BU, Goldgar DE, Kroese J, Lotz W (1986). Nonverbal intelligence and academic achievement in the hearing impaired. Volta Rev, 88, 151-158.
  316. Fain PR, Goldgar DE (1986). A nonparametric test of heterogeneity of family risk. Genet Epidemiol Suppl, 1, 61-6.
  317. Goldgar DE, Fain PR (1986). Multipoint analysis of chromosome 11p markers. Genet Epidemiol Suppl, 1, 141-6.
  318. Borkowski WJ Jr, Goldgar DE, Gorga MP, Brookhouser PE, Worthington DW (1985 May-Jun). Cerebrospinal fluid parameters and auditory brainstem responses following meningitis. Pediatr Neurol, 1(3), 134-9.
  319. Gorga MP, Worthington DW, Reiland JK, Beauchaine KA, Goldgar DE (1985 Mar-Apr). Some comparisons between auditory brain stem response thresholds, latencies, and the pure-tone audiogram. Ear Hear, 6(2), 105-12.
  320. Gallagher JC, Goldgar DE, Mahoney P, McGill J (1985). Measurement of spine density in normal and osteoporotic subjects using computerized tomography. Relationship of spine density to fracture threshold and fracture index. J Comput Assist Tomogr, 9(3), 634-635.
  321. Watson BU, Goldgar DE (1985). A note on the use of the Hiskey-Nebraska test of learning aptitude with deaf children. Lang Speech Hear Serv Sch, 16, 53-57.
  322. Fain PR, Goldgar DE (1985). Genetic Analysis Workshop III: A biological model. Genetic Epidemiology. Genet Epidemiol, 2, 215-216.
  323. Goldgar DE, Fain PR (1984). Genetic Analysis Workshop II: results of incorporating a linkage disequilibrium parameter. Genet Epidemiol, 1(2), 179-82.
  324. Goldgar DE (1984). Collection and analysis of pedigree data. Birth Defects Orig Artic Ser, 20(6), 61-76.
  325. Watson BU, Goldgar DE, Ryschon KL (1983 Dec). Subtypes of reading disability. J Clin Neuropsychol, 5(4), 377-99.
  326. Lynch HT, Fain PR, Goldgar DE, Albano WA, Malliard JA, McKenna P (1982). Familial breast cancer and its recognition in an oncology clinic. Cancer, 47, 2730-2739.
  327. Goldgar DE, Kimberling WJ (1981). Genetic expectations of polar body twinning. Acta Genet Med Gemellol (Roma), 30(4), 257-66.
  328. Kimberling WJ, Goldgar DE (1980). Utility of genetic markers in the study of human resemblance. Acta Genet Med Gemellol (Roma), 29(4), 255-62.
  329. Zerbe GO, Goldgar DE (1980). Comparison of intraclass correlation coefficients with the ratio of two independent F-statistics. Comm Stat Theor Meth, A9(15), 1641-1655.

Review

  1. Avard D, Bridge P, Bucci LM, Chiquette J, Dorval M, Durocher F, Easton D, Godard B, Goldgar D, Knoppers BM, Laframboise R, Lesperance B, Plante M, Tavtigian SV, Vezina H, Wilson B, Simard J (2006). Partnering in oncogenetic research--the INHERIT BRCAs experience: opportunities and challenges. [Review]. Fam Cancer, 5(1), 3-13.
  2. Goldgar DE (2002 Jan). Population aspects of cancer genetics. [Review]. Biochimie, 84(1), 19-25.
  3. Jefferies S, Eeles R, Goldgar D, AHern R, Henk JM, Gore M (1999 Feb). The role of genetic factors in predisposition to squamous cell cancer of the head and neck. [Review]. Br J Cancer, 79(5-6), 865-7.
  4. Eeles RA, Stratton MR, Goldgar DE, Easton DF (1994). The genetics of familial breast cancer and their practical implications. [Review]. Eur J Cancer, 30A(9), 1383-90.

Book Chapter

  1. Goldgar DE (2000). Genetic susceptibility to common cancers: a model for genetics of a complex trait. In Bishop DT, Sham P (Eds.), Genetic analysis of multifactorial diseases (pp. 63-83). BIOS Scientific Publishers Ltd.
  2. Goldgar DE (1998). Sib Pair Analysis. In Haines JL, Pericak-Vance MA (Eds.), Design of Gene Mapping Studies for Complex Human Diseases. New York: John Wiley & Sons Inc.
  3. Goldgar DE, Steele L, Neuhausen S, Cannon-Albright L, Lewis CM Skolnick M (1996). Breast and ovarian Cancer in Utah kindreds with three BRCA1 mutations. In Sharp HF, Blackett E, Leake R, Berek J (Eds.), Ovarian Cancer 4 (pp. 49-59). London, UK: Chapman Hall.
  4. Goldgar DE (1996). Identification of women at high risk of breast cancer due to inherited susceptibility. In Maltoni C, Soffritti M, Davis W (Eds.), The Scientific Bases of Cancer Chemoprevention, International Congress Series 1120, Excerpta Medica. BV, Amsterdam: Elsevier Science.
  5. Goldgar DE, Stratton MR Eeles RA (1996). Familial breast cancer. In Eeles RA, Ponder BAJ, Easton DF, Horwich A (Eds.), Genetic Predisposition to Cancer (pp. 227-238). London, UK: Chapman and Hall.
  6. Goldgar DE, Rowe K, Lewis CM, McDonald M, Gholami K, Cannon-Albright L, Skolnick M (1995). Genetic epidemiology of familial ovarian cancer in Utah. In Sharp F, Mason P, Blackett T, Berek J (Eds.), Ovarian Cancer - 3 (pp. 13-21). Chapman & Hall Medical.
  7. Lewis CM, Goldgar DE, Cannon-Albright LA, Skolnick MH (1993). Genetic analysis of cancer and precursor lesions. In PA Marks, H Turler, R Weil (Eds.), Precancerous Lesions: A Multidisciplinary Approach (pp. 69-77). Ares-Serono Symposia Publications: Christengraf Press .
  8. Cannon-Albright LA, Bishop DT, Goldgar DE, Skolnick MH (1991). Genetic epidemiology of cancer and predisposing lesions. In HT Lynch, P Tautu (Eds.), Recent Progress in the Genetic Epidemiology of Cancer (pp. pp57-65). Berlin Heidelberg: Springer-Verlag.
  9. Smith SD, Goldgar DE, Pennington BF, Kimberling WJ, Lubs HA (1986). Analysis of subtypes of specific reading diability: Genetic and cluster analytic approaches. In GT Pavlidis, DF Fisher (Eds.), Dyslexia: Its Neuropsychology and Treatment. Chichester, UK: John Wiley.
  10. Smith SD, Kimberling WJ, Goldgar DE, Pennington BF, Lubs HA (1985). The use of linkage analysis in the study of behavioral and cognitive disorder. In D Gray, R Plomin, J Johnston (Eds.), Developmental behavior genetics, Behavior Analysis, and Learning. Hillsdale, NJ: Lawrence Earlbaum Assoc.
  11. Smith SD, Goldgar DE (1985). Single gene analyses and their application to learning disabilities. In S Smith (Ed.), Genetics and Learning Disabilities. San Diego, CA: College Hill Press.

Conference Proceedings

  1. Shugart Y, Teare D, Cour C, Renard H, Bonnardel C, Sibert A, Easton D, Goldgar D (1998). Mapping of non-BRCA 1/2 breast cancer genes. Proceeding of the UICC Symposium, Familial Cancer Prevention, Kobe, Japan.

Letter

  1. Antoniou A, Anton-Culver H, Borowsky A, Broeders M, Brooks J, Chiarelli A, Chiquette J, Cuzick J, Delaloge S, Devilee P, Dorval M, Easton D, Eisen A, Eklund M, Eloy L, Esserman L, Garcia-Closas M, Goldgar D, Hall P, Knoppers BM, Kraft P, La Croix A, Madalensky L, Mavaddat N, Mittman N, Nabi H, Olopade O, Pashayan N, Schmidt M, Shieh Y, Simard J, Stover-Fiscallini A, Tice JA, Vant Veer L, Wenger N, Wolfson M, Yau C, Ziv E (2019 Mar). A response to "Personalised medicine and population health: breast and ovarian cancer" [Letter to the editor]. Hum Genet, 138(3), 287-289.
  2. Spurdle AB, Goldgar DE, Easton DF (2017 Aug 24). More on Co-Occurrence of COMT and BRCA1/2 Variants in a Population [Letter to the editor]. N Engl J Med, 377(8), 795.
  3. Duffy K, Hyde MA, Tanner B, Goldgar D, Bowen AR, Florell SR, Bowen GM (2010 Oct). Anatomic variability in superficial blood vessel and lymphatic vessel density [Letter to the editor]. J Cutan Pathol, 37(10), 1108-9.
  4. Goldgar D, Venne V, Conner T, Buys S (2007 Aug). BRCA phenocopies or ascertainment bias? [Letter to the editor]. J Med Genet, 44(8), e86; author reply e88.
  5. Narod S, Ford D, Devilee P, Barkardottir RB, Eyfjord J, Lenoir G, Serova O, Easton D, Goldgar D (1995 Oct). Genetic heterogeneity of breast-ovarian cancer revisited. Breast Cancer Linkage Consortium [Letter to the editor]. Am J Hum Genet, 57(4), 957-8.

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