Craig Teerlink

Craig Teerlink, PhD

Languages spoken: English

Academic Information

Departments Primary - Internal Medicine , Adjunct - Family & Preventive Medicine

Divisions: Public Health , Epidemiology

Academic Office Information

craig.teerlink@utah.edu

Craig Teerlink, PhD, is a Research Assistant Professor in the Division of Genetic Epidemiology in the Department of Medicine. As a research track assistant professor, his research interests include gene discovery in a variety of complex diseases.

Dr. Teerlink’s research has relied heavily on the unique resources that are available at the University of Utah including genealogical and phenotype records contained in the Utah Population Database and genotype/sequence data collected over the last several decades at the Division of Genetic Epidemiology. His research has covered a range of activities contributing to gene discovery including familial aggregation, gene localization, and analysis of sequence data.

Dr. Teerlink received his PhD from the University of Utah where he received graduate training in statistics and biomedical informatics.

Education History

Undergraduate University of Utah, Department of Economics
 BS
Graduate Training University of Utah, Department of Mathematics
 MS
Doctoral Training University of Utah, Department of Biomedical Informatics
 PhD

Selected Publications

Journal Article

  1. Allen-Brady K, Norton PA, Farnham JM, Teerlink C, Cannon-Albright LA (2009). Significant linkage evidence for a predisposition gene for pelvic floor disorders on chromosome 9q21. Am J Hum Genet, 84(5), 678-82.
  2. Ioannidis NM, Rothstein JH, Pejaver V, Middha S, McDonnell SK, Baheti S, Musolf A, Li Q, Holzinger E, Karyadi D, Cannon-Albright LA, Teerlink CC, Stanford JL, Isaacs WB, Xu J, Cooney KA, Lange EM, Schleutker J, Carpten JD, Powell IJ, Cussenot O, Cancel-Tassin G, Giles GG, MacInnis RJ, Maier C, Hsieh CL, Wiklund F, Catalona WJ, Foulkes WD, Mandal D, Eeles RA, Kote-Jarai Z, Bustamante CD, Schaid DJ, Hastie T, Ostrander EA, Bailey-Wilson JE, Radivojac P, Thibodeau SN, Whittemore AS, Sieh W (2016). REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants. Am J Hum Genet, 99(4), 877-885.
  3. LA Cannon-Albright, S Dintelman, T Maness, CC Teerlink, LJ Meyer. (2022). Evidence for excess Familial Clustering of Post Traumatic Stress Disorder in a U.S. Veterans Genealogy Resource. Am J Psychiatry, 150, 332-337.
  4. TEERLINK CC, JURYNEC MJ, HERNANDEZ R, STEVENS J, HUGHES DC, BRUNKER CP, ROWE K, GRUNWALD DJ, FACELLI JC, CANNON-ALBRIGHT LA. (2020). A role for the MEGF6 gene in predisposition to osteoporosis. Ann Hum Genet, 85, 58-72.
  5. Amin Al Olama A, Kote-Jarai Z, Schumacher FR, Wiklund F, Berndt SI, Benlloch S, Giles GG, Severi G, Neal DE, Hamdy FC, Donovan JL, Hunter DJ, Henderson BE, Thun MJ, Gaziano M, Giovannucci EL, Siddiq A, Travis RC, Cox DG, Canzian F, Riboli E, Key TJ, Andriole G, Albanes D, Hayes RB, Schleutker J, Auvinen A, Tammela TL, Weischer M, Stanford JL, Ostrander EA, Cybulski C, Lubinski J, Thibodeau SN, Schaid DJ, Sorensen KD, Batra J, Clements JA, Chambers S, Aitken J, Gardiner RA, Maier C, Vogel W, Dork T, Brenner H, Habuchi T, Ingles S, John EM, Dickinson JL, Cannon-Albright L, Teixeira MR, Kaneva R, Zhang HW, Lu YJ, Park JY, Cooney KA, Muir KR, Leongamornlert DA, Saunders E, Tymrakiewicz M, Mahmud N, Guy M, Govindasami K, O'Brien LT, Wilkinson RA, Hall AL, Sawyer EJ, Dadaev T, Morrison J, Dearnaley DP, Horwich A, Huddart RA, Khoo VS, Parker CC, Van As N, Woodhouse CJ, Thompson A, Dudderidge T, Ogden C, Cooper CS, Lophatonanon A, Southey MC, Hopper JL, English D, Virtamo J, Le Marchand L, Campa D, Kaaks R, Lindstrom S, Diver WR, Gapstur S, Yeager M, Cox A, Stern MC, Corral R, Aly M, Isaacs W, Adolfsson J, Xu J, Zheng SL, Wahlfors T, Taari K, Kujala P, Klarskov P, Nordestgaard BG, Roder MA, Frikke-Schmidt R, Bojesen SE, FitzGerald LM, Kolb S, Kwon EM, Karyadi DM, Orntoft TF, Borre M, Rinckleb A, Luedeke M, Herkommer K, Meyer A, Serth J, Marthick JR, Patterson B, Wokolorczyk D, Spurdle A, Lose F, McDonnell SK, Joshi AD, Shahabi A, Pinto P, Santos J, Ray A, Sellers TA, Lin HY, Stephenson RA, Teerlink C, Muller H, Rothenbacher D, Tsuchiya N, Narita S, Cao GW, Slavov C, Mitev V, Chanock S, Gronberg H, Haiman CA, Kraft P, Easton DF, Eeles RA (2013). A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease. Hum Mol Genet, 22(2), 408-15.
  6. Craig Teerlink, Jeffrey Stevens, Rolando Hernandez, Julio Facelli, Lisa Cannon-Albright (2021). An intronic variant in the CELF4 gene is associated with risk for colorectal cancer. Hum Mutat, 72, 101941.
  7. Eeles RA, Olama AA, Benlloch S, Saunders EJ, Leongamornlert DA, Tymrakiewicz M, Ghoussaini M, Luccarini C, Dennis J, Jugurnauth-Little S, Dadaev T, Neal DE, Hamdy FC, Donovan JL, Muir K, Giles GG, Severi G, Wiklund F, Gronberg H, Haiman CA, Schumacher F, Henderson BE, Le Marchand L, Lindstrom S, Kraft P, Hunter DJ, Gapstur S, Chanock SJ, Berndt SI, Albanes D, Andriole G, Schleutker J, Weischer M, Canzian F, Riboli E, Key TJ, Travis RC, Campa D, Ingles SA, John EM, Hayes RB, Pharoah PD, Pashayan N, Khaw KT, Stanford JL, Ostrander EA, Signorello LB, Thibodeau SN, Schaid D, Maier C, Vogel W, Kibel AS, Cybulski C, Lubinski J, Cannon-Albright L, Brenner H, Park JY, Kaneva R, Batra J, Spurdle AB, Clements JA, Teixeira MR, Dicks E, Lee A, Dunning AM, Baynes C, Conroy D, Maranian MJ, Ahmed S, Govindasami K, Guy M, Wilkinson RA, Sawyer EJ, Morgan A, Dearnaley DP, Horwich A, Huddart RA, Khoo VS, Parker CC, Van As NJ, Woodhouse CJ, Thompson A, Dudderidge T, Ogden C, Cooper CS, Lophatananon A, Cox A, Southey MC, Hopper JL, English DR, Aly M, Adolfsson J, Xu J, Zheng SL, Yeager M, Kaaks R, Diver WR, Gaudet MM, Stern MC, Corral R, Joshi AD, Shahabi A, Wahlfors T, Tammela TL, Auvinen A, Virtamo J, Klarskov P, Nordestgaard BG, Roder MA, Nielsen SF, Bojesen SE, Siddiq A, Fitzgerald LM, Kolb S, Kwon EM, Karyadi DM, Blot WJ, Zheng W, Cai Q, McDonnell SK, Rinckleb AE, Drake B, Colditz G, Wokolorczyk D, Stephenson RA, Teerlink C, Muller H, Rothenbacher D, Sellers TA, Lin HY, Slavov C, Mitev V, Lose F, Srinivasan S, Maia S, Paulo P, Lange E, Cooney KA, Antoniou AC, Vincent D, Bacot F, Tessier DC, Kote-Jarai Z, Easton DF. (2013). Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array. Nat Genet, 45(4), 385-391.
  8. Larson NB, McDonnell S, Cannon Albright L, Teerlink C, Stanford J, Ostrander EA, Isaacs WB, Xu J, Cooney KA, Lange E, Schleutker J, Carpten JD, Powell I, Bailey-Wilson JE, Cussenot O, Cancel-Tassin G, Giles GG, MacInnis RJ, Maier C, Whittemore AS, Hsieh CL, Wiklund F, Catalona WJ, Foulkes W, Mandal D, Eeles R, Kote-Jarai Z, Ackerman MJ, Olson TM, Klein CJ, Thibodeau SN, Schaid D (2017). gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels. Genetic epidemiology, 41(4), 297-308.
  9. Teerlink CC, Thomas (2010). An application of the latent p value method to assess linkage in asthma pedigrees. Human heredity, 70(1), 1-8.
  10. Teerlink C, Farnham J, Allen-Brady K, Camp NJ, Thomas A, Leachman S, Cannon-Albright (2012). A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. Human genetics, 131(1), 77-85.
  11. Jin G, Lu L, Cooney KA, Ray AM, Zuhlke KA, Lange EM, Cannon-Albright LA, Camp NJ, Teerlink CC, Fitzgerald LM, Stanford JL, Wiley KE, Isaacs SD, Walsh PC, Foulkes WD, Giles GG, Hopper JL, Severi G, Eeles R, Easton D, Kote-Jarai Z, Guy M, Rinckleb A, Maier C, Vogel W, Cancel-Tassin G, Egrot C, Cussenot O, Thibodeau SN, McDonnell SK, Schaid DJ, Wiklund F, Gronberg H, Emanuelsson M, Whittemore AS, Oakley-Girvan I, Hsieh CL, Wahlfors T, Tammela T, Schleutker J, Catalona WJ, Zheng SL, Ostrander EA, Isaacs WB, Xu (2012). Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG). Human genetics, 131(7), 1095-103.
  12. Xu J, Lange EM, Lu L, Zheng SL, Wang Z, Thibodeau SN, Cannon-Albright LA, Teerlink CC, Camp NJ, Johnson AM, Zuhlke KA, Stanford JL, Ostrander EA, Wiley KE, Isaacs SD, Walsh PC, Maier C, Luedeke M, Vogel W, Schleutker J, Wahlfors T, Tammela T, Schaid D, McDonnell SK, DeRycke MS, Cancel-Tassin G, Cussenot O, Wiklund F, Gronberg H, Eeles R, Easton D, Kote-Jarai Z, Whittemore AS, Hsieh CL, Giles GG, Hopper JL, Severi G, Catalona WJ, Mandal D, Ledet E, Foulkes WD, Hamel N, Mahle L, Moller P, Powell I, Bailey-Wilson JE, Carpten JD, Seminara D, Cooney KA, Isaacs W (2013). HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG). Human genetics, 132(1), 5-14.
  13. Teerlink CC, Thibodeau SN, McDonnell SK, Schaid DJ, Rinckleb A, Maier C, Vogel W, Cancel-Tassin G, Egrot C, Cussenot O, Foulkes WD, Giles GG, Hopper JL, Severi G, Eeles R, Easton D, Kote-Jarai Z, Guy M, Cooney KA, Ray AM, Zuhlke KA, Lange EM, Fitzgerald LM, Stanford JL, Ostrander EA, Wiley KE, Isaacs SD, Walsh PC, Isaacs WB, Wahlfors T, Tammela T, Schleutker J, Wiklund F, Grönberg H, Emanuelsson M, Carpten J, Bailey-Wilson J, Whittemore AS, Oakley-Girvan I, Hsieh CL, Catalona WJ, Zheng SL, Jin G, Lu L, Xu J, International Consortium for Prostate Cancer Genetics., Camp NJ, Cannon-Albright L (2014). Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease. Human genetics, 133(3), 347-56.
  14. Teerlink CC, Leongamornlert D, Dadaev T, Thomas A, Farnham J, Stephenson RA, Riska S, McDonnell SK, Schaid DJ, Catalona WJ, Zheng SL, Cooney KA, Ray AM, Zuhlke KA, Lange EM, Giles GG, Southey MC, Fitzgerald LM, Rinckleb A, Luedeke M, Maier C, Stanford JL, Ostrander EA, Kaikkonen EM, Sipeky C, Tammela T, Schleutker J, Wiley KE, Isaacs SD, Walsh PC, Isaacs WB, Xu J, Cancel-Tassin G, Cussenot O, Mandal D, Laurie C, Laurie C, PRACTICAL consortium., International Consortium for Prostate Cancer Genetics., Thibodeau SN, Eeles RA, Kote-Jarai Z, Cannon-Albright (2016). Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21. Human genetics, 135(8), 923-38.
  15. Tashjian RZ, Farnham JM, Albright FS, Teerlink CC, Cannon-Albright L (2009). Evidence for an inherited predisposition contributing to the risk for rotator cuff disease. The Journal of bone and joint surgery. American volume, 91(5), 1136-42.
  16. Smith KM, Hotaling JM, Presson AP, Zhang C, Horns JJ, Cannon-Alright LA, Teerlink CC, Tashjian RZ, Chalmers PN (2022). Sex Hormone Deficiency Associates with Rotator Cuff Repair and Revision after Rotator Cuff Repair. The Journal of bone and joint surgery. American volume, 104(9), 774-779.
  17. Cannon-Albright LA, Teerlink CC, Farnham JM, Thomas AW, Zone JJ, Leachman S (2013). Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21. The Journal of investigative dermatology, 133(1), 128-34.
  18. Teerlink CC, Huff C, Stevens J, Yu Y, Holmen SL, Silvis MR, Trombetti K, Zhao H, Grossman D, Farnham JM, Wen J, Facelli JC, Thomas A, Babst M, Florell SR, Meyer L, Zone JJ, Leachman S, Cannon-Albright L (2018). A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant Melanoma. Journal of the National Cancer Institute, 110(12), 1380-1385.
  19. Abbott D, Brockmeyer D, Neklason DW, Teerlink C, Cannon-Albright L (2018). Population-based description of familial clustering of Chiari malformation Type I. Journal of neurosurgery, 128(2), 460-465.
  20. Kim, Y., Sharp, S.J., Hwang, S., Luo, S., Au Yeung, S.L., & Teerlink, C.C (2021). Genetic risk, muscle strength and incident stroke: findings from the UK Biobank study. Mayo Clinic proceedings,
  21. Cannon-Albright LA, Foster NL, Schliep K, Farnham JM, Teerlink CC, Kaddas H, Tschanz J, Corcoran C, Kauwe JS (2019). Relative risk for Alzheimer disease based on complete family history. Neurology, 92(15), e1745-e1753.
  22. Allen-Brady K, Cannon-Albright L, Farnham JM, Teerlink C, Vierhout ME, van Kempen LC, Kluivers KB, Norton P (2011). Identification of six loci associated with pelvic organ prolapse using genome-wide association analysis. Obstetrics and gynecology, 118(6), 1345-53.
  23. Cannon-Albright LA, Farnham JM, Bailey M, Albright FS, Teerlink CC, Agarwal N, Stephenson RA, Thomas (2014). Identification of specific Y chromosomes associated with increased prostate cancer risk. The Prostate, 74(9), 991-8.
  24. Albright F, Stephenson RA, Agarwal N, Teerlink CC, Lowrance WT, Farnham JM, Albright L (2015). Prostate cancer risk prediction based on complete prostate cancer family history. The Prostate, 75(4), 390-8.
  25. Teerlink CC, Hegewald MJ, Cannon-Albright L (2007). A genealogical assessment of heritable predisposition to asthma mortality. American journal of respiratory and critical care medicine, 176(9), 865-70.
  26. Teerlink CC, Camp NJ, Bansal A, Crapo R, Hughes D, Kort E, Rowe K, Cannon-Albright L (2009). Significant evidence for linkage to chromosome 5q13 in a genome-wide scan for asthma in an extended pedigree resource. European journal of human genetics, 17(5), 636-43.
  27. Potrony M, Puig-Butille JA, Farnham JM, Giménez-Xavier P, Badenas C, Tell-Martí G, Aguilera P, Carrera C, Malvehy J, Teerlink CC, Puig (2018). Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q. European journal of human genetics, 26(8), 1188-1193.
  28. Teerlink CC, Cannon-Albright LA, Tashjian R (2015). Significant association of full-thickness rotator cuff tears and estrogen-related receptor-ß (ESRRB). Journal of shoulder and elbow surgery, 24(2), e31-5.
  29. Tashjian RZ, Granger EK, Zhang Y, Teerlink CC, Cannon-Albright L (2016). Identification of a genetic variant associated with rotator cuff repair healing. Journal of shoulder and elbow surgery, 25(6), 865-72.
  30. Teerlink CC, Lisa A Cannon-Albright LA, Tashjian R (2014). Significant Association of Full-Thickness Rotator Cuff Tears and ESRRB (Estrogen-related Receptor Beta). Journal of shoulder and elbow surgery,
  31. Tashjian RZ, Granger EK, Farnham JM, Cannon-Albright LA, Teerlink C (2016). Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms. Journal of shoulder and elbow surgery, 25(2), 174-9.
  32. Tashjian R, Kim SK, Roche MD, Jones KB, Teerlink C (2020). Genetic Variants Associated With Rotator Cuff Tearing Utilizing Multiple Population-Based Genetic Resources. Journal of shoulder and elbow surgery,
  33. Teerlink CC, Bernhisel R, Cannon-Albright LA, Rollins M (2018). A genealogical assessment of familial clustering of anorectal malformations. Journal of human genetics, 63(10), 1029-1034.
  34. Cai Z, Thomas A, Teerlink C, Farnham JM, Cannon-Albright LA, Camp N (2012). Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees. BMC genomics, 13, 676.
  35. Albright F, Teerlink C, Werner TL, Cannon-Albright L (2012). Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site. BMC cancer, 12, 138.
  36. Teerlink CC, Albright FS, Lins L, Cannon-Albright L (2012). A comprehensive survey of cancer risks in extended families. Genetics in medicine, 14(1), 107-14.
  37. McCarthy JP, Browning WD, Teerlink C, Veit (2012). Treatment of herpes labialis: comparison of two OTC drugs and untreated controls. Journal of esthetic and restorative dentistry, 24(2), 103-9.
  38. Allen-Brady K, Horne BD, Malhotra A, Teerlink C, Camp NJ, Thomas (2007). Analysis of high-density single-nucleotide polymorphism data: three novel methods that control for linkage disequilibrium between markers in a linkage analysis. BMC proceedings, 1 Suppl 1, S160.
  39. Ridge PG, Karch CM, Hsu S, Arano I, Teerlink CC, Ebbert MTW, Murcia JDG, Farnham JM, Damato AR, Allen M, Wang X, Harari O, Fernandez VM, Guerreiro R, Bras J, Hardy J, Munger R, Norton M, Sassi C, Singleton A, Younkin SG, Dickson DW, Golde TE, Price ND, Ertekin-Taner N, Cruchaga C, Goate AM, Corcoran C, Tschanz J, Cannon-Albright LA, Kauwe JSK, Alzheimer's Disease Neuroimaging Initiative (2018). Correction to: Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience. Genome medicine, 10(1), 4.
  40. Gusev A, Shi H, Kichaev G, Pomerantz M, Li F, Long HW, Ingles SA, Kittles RA, Strom SS, Rybicki BA, Nemesure B, Isaacs WB, Zheng W, Pettaway CA, Yeboah ED, Tettey Y, Biritwum RB, Adjei AA, Tay E, Truelove A, Niwa S, Chokkalingam AP, John EM, Murphy AB, Signorello LB, Carpten J, Leske MC, Wu SY, Hennis AJ, Neslund-Dudas C, Hsing AW, Chu L, Goodman PJ, Klein EA, Witte JS, Casey G, Kaggwa S, Cook MB, Stram DO, Blot WJ, Eeles RA, Easton D, Kote-Jarai Z, Al Olama AA, Benlloch S, Muir K, Giles GG, Southey MC, Fitzgerald LM, Gronberg H, Wiklund F, Aly M, Henderson BE, Schleutker J, Wahlfors T, Tammela TL, Nordestgaard BG, Key TJ, Travis RC, Neal DE, Donovan JL, Hamdy FC, Pharoah P, Pashayan N, Khaw KT, Stanford JL, Thibodeau SN, McDonnell SK, Schaid DJ, Maier C, Vogel W, Luedeke M, Herkommer K, Kibel AS, Cybulski C, Wokolorczyk D, Kluzniak W, Cannon-Albright L, Teerlink C, Brenner H, Dieffenbach AK, Arndt V, Park JY, Sellers TA, Lin HY, Slavov C, Kaneva R, Mitev V, Batra J, Spurdle A, Clements JA, Teixeira MR, Pandha H, Michael A, Paulo P, Maia S, Kierzek A, PRACTICAL consortium., Conti DV, Albanes D, Berg C, Berndt SI, Campa D, Crawford ED, Diver WR, Gapstur SM, Gaziano JM, Giovannucci E, Hoover R, Hunter DJ, Johansson M, Kraft P, Le Marchand L, Lindström S, Navarro C, Overvad K, Riboli E, Siddiq A, Stevens VL, Trichopoulos D, Vineis P, Yeager M, Trynka G, Raychaudhuri S, Schumacher FR, Price AL, Freedman ML, Haiman CA, Pasaniuc (2016). Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation. Nature communications, 7, 10979.
  41. Lisa A Cannon-Albright, Craig C Teerlink, Jeff Stevens, Franklin Huang, Csilla Sipeky, Johanna Schleutker, Rolando Hernandez, Julio Facelli, Neeraj Agarwal, Donald L Trum (2023). A rare variant in ERF (rs144812092) predisposes to prostate and bladder cancers. Cancers, 13(10), 2399.
  42. Teerlink C, Nelson Q, Burt R, Cannon-Albright (2014). Significant evidence of linkage for a gene predisposing to colorectal cancer and multiple primary cancers on 22q11. Clinical and translational gastroenterology, 5, e50.
  43. Kar SP, Beesley J, Amin Al Olama A, Michailidou K, Tyrer J, Kote-Jarai Z, Lawrenson K, Lindstrom S, Ramus SJ, Thompson DJ, ABCTB Investigators., Kibel AS, Dansonka-Mieszkowska A, Michael A, Dieffenbach AK, Gentry-Maharaj A, Whittemore AS, Wolk A, Monteiro A, Peixoto A, Kierzek A, Cox A, Rudolph A, Gonzalez-Neira A, Wu AH, Lindblom A, Swerdlow A, AOCS Study Group & Australian Cancer Study (Ovarian Cancer)., APCB BioResource., Ziogas A, Ekici AB, Burwinkel B, Karlan BY, Nordestgaard BG, Blomqvist C, Phelan C, McLean C, Pearce CL, Vachon C, Cybulski C, Slavov C, Stegmaier C, Maier C, Ambrosone CB, Høgdall CK, Teerlink CC, Kang D, Tessier DC, Schaid DJ, Stram DO, Cramer DW, Neal DE, Eccles D, Flesch-Janys D, Edwards DR, Wokozorczyk D, Levine DA, Yannoukakos D, Sawyer EJ, Bandera EV, Poole EM, Goode EL, Khusnutdinova E, Høgdall E, Song F, Bruinsma F, Heitz F, Modugno F, Hamdy FC, Wiklund F, Giles GG, Olsson H, Wildiers H, Ulmer HU, Pandha H, Risch HA, Darabi H, Salvesen HB, Nevanlinna H, Gronberg H, Brenner H, Brauch H, Anton-Culver H, Song H, Lim HY, McNeish I, Campbell I, Vergote I, Gronwald J, Lubi'ski J, Stanford JL, Benítez J, Doherty JA, Permuth JB, Chang-Claude J, Donovan JL, Dennis J, Schildkraut JM, Schleutker J, Hopper JL, Kupryjanczyk J, Park JY, Figueroa J, Clements JA, Knight JA, Peto J, Cunningham JM, Pow-Sang J, Batra J, Czene K, Lu KH, Herkommer K, Khaw KT, kConFab Investigators., Matsuo K, Muir K, Offitt K, Chen K, Moysich KB, Aittomäki K, Odunsi K, Kiemeney LA, Massuger LF, Fitzgerald LM, Cook LS, Cannon-Albright L, Hooning MJ, Pike MC, Bolla MK, Luedeke M, Teixeira MR, Goodman MT, Schmidt MK, Riggan M, Aly M, Rossing MA, Beckmann MW, Moisse M, Sanderson M, Southey MC, Jones M, Lush M, Hildebrandt MA, Hou MF, Schoemaker MJ, Garcia-Closas M, Bogdanova N, Rahman N, NBCS Investigators., Le ND, Orr N, Wentzensen N, Pashayan N, Peterlongo P, Guénel P, Brennan P, Paulo P, Webb PM, Broberg P, Fasching PA, Devilee P, Wang Q, Cai Q, Li Q, Kaneva R, Butzow R, Kopperud RK, Schmutzler RK, Stephenson RA, MacInnis RJ, Hoover RN, Winqvist R, Ness R, Milne RL, Travis RC, Benlloch S, Olson SH, McDonnell SK, Tworoger SS, Maia S, Berndt S, Lee SC, Teo SH, Thibodeau SN, Bojesen SE, Gapstur SM, Kjær SK, Pejovic T, Tammela TL, GENICA Network., PRACTICAL consortium., Dörk T, Brüning T, Wahlfors T, Key TJ, Edwards TL, Menon U, Hamann U, Mitev V, Kosma VM, Setiawan VW, Kristensen V, Arndt V, Vogel W, Zheng W, Sieh W, Blot WJ, Kluzniak W, Shu XO, Gao YT, Schumacher F, Freedman ML, Berchuck A, Dunning AM, Simard J, Haiman CA, Spurdle A, Sellers TA, Hunter DJ, Henderson BE, Kraft P, Chanock SJ, Couch FJ, Hall P, Gayther SA, Easton DF, Chenevix-Trench G, Eeles R, Pharoah PD, Lambrechts (2016). Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types. Cancer discovery, 6(9), 1052-67.
  44. Lisa A. Cannon'Albright, Craig C. Teerlink, Jeffrey Stevens, Angela K. Snow, Bryony A. Thompson, Russell Bell, Kim N. Nguyen, Nykole R. Sargent, Wendy K. Kohlmann, Deborah W. Neklason, Sean V. Tavtigia (2020). FANCM c5791CT stopgain mutation (rs144567652) is a familial colorectal cancer risk factor. Molecular genetics & genomic medicine, 8, e1532.
  45. Spiker WR, Brodke DS, Goz V, Lawrence B, Teerlink CC, Cannon-Albright L (2018). Evidence of an Inherited Predisposition for Spinal Cord Tumors. Global spine journal, 8(4), 340-344.
  46. Tashjian RZ, Farnham JM, Granger EK, Teerlink CC, Cannon-Albright L (2016). Evidence for an Environmental and Inherited Predisposition Contributing to the Risk for Global Tendinopathies or Compression Neuropathies in Patients With Rotator Cuff Tears. Orthopaedic journal of sports medicine, 4(4), 2325967116642173.
  47. Cannon-Albright LA, Dintelman S, Maness T, Cerny J, Thomas A, Backus S, Farnham JM, Teerlink CC, Contreras J, Kauwe JK, Meyer LJ (2018). A Population Genealogy Resource shows evidence of familial clustering for Alzheimer's Disease. Neurology. Genetics,
  48. Cannon-Albright LA, Dintelman S, Maness T, Cerny J, Thomas A, Backus S, Farnham JM, Teerlink CC, Contreras J, Kauwe JSK, Meyer L (2018). Population genealogy resource shows evidence of familial clustering for Alzheimer disease. Neurology. Genetics, 4(4), e249.
  49. Patel D, Mez J, Vardarajan BN, Staley L, Chung J, Zhang X, Farrell JJ, Rynkiewicz MJ, Cannon-Albright LA, Teerlink CC, Stevens J, Corcoran C, Gonzalez Murcia JD, Lopez OL, Mayeux R, Haines JL, Pericak-Vance MA, Schellenberg G, Kauwe JSK, Lunetta KL, Farrer LA, Alzheimer's Disease Sequencing Project (2019). Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry. JAMA network open, 2(3), e191350.
  50. Craig C. Teerlink, Elizabeth Ward, Justin B. Miller, Lyndsay A. Staley, Jeffrey Stevens, Justina P. Tavana, Matthew Cloward, Madeline Page, Louisa Dayton, Alzheimer's Disease Genetics Consortium, Lisa A. Cannon-Albright, and John S.K. Kauwe (2022). Analysis of high-risk pedigrees identifies twelve candidate variants for Alzheimer’s Disease. Alzheimer's & dementia, 18(2), 307-317.
  51. Talwar JV, Laub D, Pagadala MS, Castro A, Lewis M, Luebeck GE, Gorman BR, Pan C, Dong FN, Markianos K, Teerlink CC, Lynch J, Hauger R, Pyarajan S, Tsao PS, Morris GP, Salem RM, Thompson WK, Curtius K, Zanetti M, Carter (2023). Autoimmune alleles at the major histocompatibility locus modify melanoma susceptibility. American journal of human genetics, 13(S0002-9297), 00170-2.
  52. Cannon-Albright LA, Teerlink CC, Stevens J, Facelli JC, Carr SR, Allen-Brady K, Puri S, Bailey-Wilson JE, Musolf AM; Genetic Epidemiology of Lung Cancer Consortium; Akerley (2023). A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall-cell lung cancer. International journal of cancer, 15(153), 364-372.
  53. Teerlink CC, Miller JB, Vance EL, Staley LA, Stevens J, Tavana JP, Cloward ME, Page ML, Dayton L; Alzheimer's Disease Genetics Consortium, Cannon-Albright LA, Kauwe JSK (2023). Analysis of high-risk pedigrees identifies 11 candidate variants for Alzheimer’s disease. alzheimer's dementia, 18(2), 307-317.
  54. Valentine D, Teerlink CC, Farnham JM, Rowe K, Kaddas H, Tschanz J, Kauwe JSK, Cannon-Albright LA (2022). Comorbidity and Cancer Disease Rates among Those at High-Risk for Alzheimer's Disease: A Population Database Analysis. Int J Environ Res Public Health. International journal of environmental research and public health, 19(24), 16419.
  55. Cannon-Albright LA, Stevens J, Facelli JC, Teerlink CC, Allen-Brady K, Agarwal N (2023). High-Risk Pedigree Study Identifies LRBA (rs62346982) as a Likely Predisposition Variant for Prostate Cancer. Cancers, 15(7), 2085.
  56. Heather M Ochs-Balcom, Leah Preus, Zhaohui Du, Robert C Elston, Craig C Teerlink, Guochong Jia, Xingyi Guo, Qiuyin Cai, Jirong Long, Jie Ping, Bingshan Li, Daniel O Stram, Xiao-Ou Shu, Maureen Sanderson, Guimin Gao, Thomas Ahearn, Kathryn L Lunetta, Gary Zirpoli, Melissa A Troester, Edward A Ruiz-Narváez, Stephen A Haddad, Jonine Figueroa, Esther M John, Leslie Bernstein, Jennifer J Hu, Regina G Ziegler, Sarah Nyante, Elisa V Bandera, Sue A Ingles, Nicholas Mancuso, Michael F Press, Sandra L Deming, Jorge L Rodriguez-Gil, Song Yao, Temidayo O Ogundiran, Oladosu Ojengbede, Manjeet K Bolla, Joe Dennis, Alison M Dunning, Douglas F Easton, Kyriaki Michailidou, Paul D P Pharoah, Dale P Sandler, Jack A Taylor, Qin Wang, Katie M O'Brien, Clarice R Weinberg, Cari M Kitahara, William Blot, Katherine L Nathanson, Anselm Hennis, Barbara Nemesure, Stefan Ambs, Lara E Sucheston-Campbell, Jeannette T Bensen, Stephen J Chanock, Andrew F Olshan, Christine B Ambrosone, Olufunmilayo I Olopade, the Ghana Breast Health Study Team, David V Conti, Julie Palmer, Montserrat García-Closas, Dezheng Huo, Wei Zheng, Christopher Haima (2024). Novel breast cancer susceptibility loci under linkage peaks identified in African ancestry consortia. Human molecular genetics, ddae002.
  57. Oxnard GR, Chen R, Phar JC, Koeller DR, Bertram AA, Dahlberg SE, Rainville I, Shane-Carson K, Taylor KA, Sable-Hunt A, Sholl LM, Teerlink CC, Thomas A, Cannon-Albright LA, Fay AP, Ashton-Prolla P, Yang H, Salvatore MM, Addario BJ, Jane PA, Carbone DP, Weisner GL, Garber J (2023). Germline EGFR mutations and familial lung cancer. Journal of clinical oncology, 41(34),
  58. Thompson BA, Snow AK, Koptiuch C, Kohlmann WK, Mooney R, Johnson S, Huff CD, Yu Y, Teerlink CC, Feng BJ, Neklason DW, Cannon-Albright LA, Tavtigian S (2020). A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposis. Clinical genetics, 97(6), 943-944.
  59. Lee KM, Nelson T, Bryant A, Teerlink C, Gulati R, Pagadala M, Tcheandjieu C, Pridgen KM, DuVall SL, Yamoah K, Vassy JL, Seibert TM, Hauger R, Rose BS, Lynch J (2024). Genetic risk and likelihood of prostate cancer detection on first biopsy by ancestry. Journal of the National Cancer Institute, djae002.
  60. Cannon-Albright LA, Stevens J, Teerlink CC, Facelli JC, Allen-Brady K, Welm A (2023). A rare variant in MDH2 (rs111879470) is associated with predisposition to recurrent breast cancer in an extended high-risk pedigree. Cancers, 15(24), 5851.
  61. Davis SM, Teerlink CC, Lynch JA, Klamut N, Gorman BR, Pagadala M, Panizzon MS, Merritt VC, Genovese G, Pyarajan S, Ross JL, Hauger R (2024). An Extra X Chromosome Among Adult Women in the Million Veteran Program: A More Benign Perspective of Trisomy X. American journal of medical genetics. Part C, Seminars in medical genetics,
  62. McKay RR, Nelson TJ, Pagadala MS, Teerlink CC, Gao A, Bryant AK, Agiri FY, Guram K, Thompson RF, Pridgen KM, Seibert TM, Lee KM, Carter H, Lynch JA, Hauger RL, Rose BS (2024). Adrenal-permissive germline hsd3b1 allele and prostate cancer outcomes. JAMA network open, 7(3), e242976.
  63. Tashjian RZ, Jurynec MJ, Christy K, Stevens J, Teerlink CC, Cannon-Albright LA, Allen-Brady (2024). Identification of Rare Genetic Variants for Rotator Cuff Tearing and Repair in High-Risk Pedigrees. JSES international,
  64. Davis SM, Teerlink C, Lynch JA, Gorman BR, Pagadala M, Liu A, Panizzon MS, Merritt VC, Genovese G, Ross JL, Hauger R (2024). Prevalence, Morbidity, and Mortality of Men With Sex Chromosome Aneuploidy in the Million Veteran Program Cohort. JAMA network open, 7(3), e244113.
  65. Kaplan DE, Teerlink C, Vujkovic M, Devineni P, Sendamarai A, Purushotham K, DuVall S, Schwantes-An THL, Norden-Krichmar T, Morgan TR, Anglin T, Lynch J, Tsao P, Pyarajan S, Voight BF, Chang K (2024). Clinical and Genetic Risk Factors for Progressive Fibrosis in Metabolic Dysfunction-Associated Steatotic Liver Disease. Hepatology communications, 8(7), e0487.
  66. Pagadala MS, Teerlink CC, Jasuja GK, Palnati M, Anglin-Foote T, Chang N, Deka R, Lee KM, Agiri FY, Seibert TM, Rose BS, Pridgen KM, Lynch JA, Carter HK, Panizzon MS, Hauger R Discovery of Novel Trans-Ancestry and Ancestry-Specific Gene Loci for Androgen Levels and Hypogonadism in a Multi-Ancestral Analysis of Million Veteran Program Men. Nature communications,
  67. Craig C. Teerlink*, Shanlee M. Davis*, Aoxing Liu*, Dana M. Lapato, Bryan Gorman, Giulio Genovese, Madhurbain Singh, Mary P. Reeve, Amanda Elswick E. Gentry, Kati M. Donner, Timo P. Sipilä, Awaisa Ghazal, Meghana S. Pagadala, Matthew S. Panizzon, Eva E. Lancaster, FinnGen, banner authorship UKB working group authorship, Chris Chatzinakos, Andrea Ganna, Tim B. Bigdeli, Mark J. Daly, Julie A. Lynch, Judith Ross, Roseann E. Peterson, Richard L. Hauger. *Joint first authors Prevalence and disease risks of male and female sex chromosome trisomies in 1.5 million participants of MVP, Finngen, and UKBiobank. American journal of human genetics,
  68. Danielle Candelieri-Surette, JongSoo Lee, Julie Lynch, Nai-Chung Chang, Tyler Nelson, Craig Teerlink, Camilla Pimentel, Martin Schoen, Dan Berlowit Epidemiology of Metastatic Castration-Resistant Prostate Cancer in Veterans Nationwide. Journal of the National Comprehensive Cancer Network,
  69. Taylor B Crawford, Tyler Nelson, Roshan Karunamuni, Heena Desai, Ryan Hausler, Craig Teerlink, Hannah Carter, Meghana S. Pagadala, Patrick R. Alba, Scott L. DuVall, Morgan E. Danowski, Charles A. Brunette, Dmitry Ratner, Isla P. Garraway, Brent S. Rose, Jeffrey R. Smith, Kathleen A. Cooney, Jason L. Vassy, Richard L. Hauger, Julie A. Lynch, Tyler M. Seibert, Kara N. Maxwel Association of HOXB13 G84E with prostate cancer among 592,158 men. Journal of the National Comprehensive Cancer Network,
  70. Sony Tuteja, William J. O'Brien, Jeffrey P. Ferraro, Scott M. Damrauer, Kamal Itani, Benjamin Voight, Craig C. Teerlink, Julie A. Lynch, Scott L. DuVall, Timothy Strebel, Michael J. Kim, Mark A. Wilson, Thomas W. Barrett, Million Veteran Progra Drug-gene interactions and clinical outcomes after vascular surgery in the Million Veteran Program. JAMA surgery,
  71. Danielle Candelieri-Surette, Nina Cheranda, JongSoo Lee, Craig C. Teerlink, Camilla Pimentel, Julie A. Lynch, Dan Berlowitz, Martin W. Schoe The Impact of Race on Survival and Treatment in Veterans Treated for Metastatic Castration-Resistant Prostate Cancer. Journal of the National Comprehensive Cancer Network,

Abstract

  1. Teerlink CC, Cryer ME, Thomas (2009). Interpreting the mod score statistic in a genomewide scan for asthma.
  2. Albright F, Teerlink CC, Farnham J, Backus S, Cannon-Albright L (2009). Reconstituting genealogical information from a multipurpose data resource.
  3. Teerlink CC, Thomas (2008). An application of the latent p-value method to assess linkage in asthma pedigrees.
  4. Teerlink CC, Camp NJ, Cannon-Albright L (2006). Genome-wide linkage analysis for asthma predisposition loci in an extended pedigree resource.
  5. Teerlink CC, Cannon-Albright L (2006). A genealogical assessment of heritable predisposition to asthma mortality.
  6. Neklason D, Done M, Sargent N, Bailey M, Teerlink C, Burt R (2013). Exome sequencing of affected individuals in large multigenerational colorectal cancer kindred.
  7. Teerlink CC, Farham JM, Tashjian R, Cannon-Albright L (2013). Evidence for a genetic contribution to rotator cuff disease in a new population genealogy at the Veterans Administration.
  8. Cannon-Albright LA, Farnham JM, Teerlink CC, Stephenson R (2013). Identification of Y chromosomes associated with risk for prostate cancer.
  9. Teerlink CC, Nelson QC, Neeraj Agarwal N, Stephenson RA, Cannon-Albright L (2013). A population-based analysis of clustering identifies a strong genetic contribution to recurrent prostate cancer.
  10. Neklason DW, Gilcrease GW, Sargent NR, Snow A, Teerlink C, M. Bailey M, Burt R (2013). Exome Sequencing of Family with Carcinoid Cancers.
  11. Schaid DJ, McDonnell SK, Sinnwell JP, Cannon Albright L, Teerlink CC, Stanford J, Ostrander E, Isaacs WB, Xu J, Cooney KA, Lange E, Schleutker J, Carpten JD, Powell I, Bailey-Wilson J, Cussenot O, Cancel-Tassin G, Giles G, Fitzgerald L, Maier C, Whittemore A, Hsieh CL, Wiklund F, Catalona WJ, Foulkes W, Mandal D, Eeles R, Thibodeau S (2014). Statistical Tests for Co-Segregation of Genetic Variants with Disease in Pedigrees.
  12. Teerlink CC, Yu YY, Fletcher PT, Cannon-Albright LA, Thomas AW (2012). A novel method to identify highly penetrant pedigree-specific facial morphological phenotypes for genetic mapping.
  13. Teerlink C, Thibodeau S, Schaid D, Cooney K, Lang E, Maier C, Stanford J, Ostrander E, Schleutker J, Cancel-Tassin G, Eeles R, Easton D, Isaacs W, Xu J, Bailey-Wilson J, Wiklund F, Whittemore A, Catalona W, Foulkes W, Camp N, Cannon-Albright L, the International Consortium for Prostate Cancer Genetic (2012). Meta-analysis of 25 prostate cancer associated SNPs in high-risk prostate cancer families: new evidence from the International Consortium for Prostate Cancer Genetics (ICPCG).
  14. Teerlink CC, Farnham J, Allen-Brady K, Horne BD, Camp NJ, Cannon-Albright L (2010). Using publicly available control data for GWAS - a simple strategy for genetic matching.
  15. Teerlink CC, Farnham J, Cannon-Albright L (2011). Significant confirmation of linkage to melanoma at 9q21 in an extended Utah pedigree.
  16. Cannon-Albright LA, Teerlink CC, Agarwal N, Stephenson (2011). Evidence for a strong genetic contribution to lethal prostate cancer.
  17. Neeraj Agarwal, Anitha Alex, James M. Farnham, Shiven B. Patel, Srinivas Kiran Tantravahi, Craig Teerlink, Frederick S. Albright, Robert A Stephenson, Lisa A Cannon-Albrigh (2015). Association of single nucleotide polymorphisms (SNPs) in ESR1 and PRMT8 and response to treatment with abiraterone acetate (AA) in men with metastatic castration refractory prostate cancer (mCRPC). No.150082.
  18. Neeraj Agarwal, Tyler Howard Buckley, James M. Farnham, Shiven B. Patel, Archana M. Agarwal, Srinivas Kiran Tantravahi, Craig Teerlink, Frederick S. Albright, Robert A Stephenson, Anitha Alex, Lisa A Cannon-Albrigh (2015). Association of single nucleotide polymorphisms (SNPs) in STS and SULT2B1 and response to androgen deprivation therapy (ADT) in men with new hormone sensitive metastatic prostate cancer (mHSPC). No. 151027.
  19. Cannon-Albright LA, Dintelman S, Maness T, Thomas A, Teerlink C, Meyer (2012). A national resource for aging research: the Veterans Administration genealogy project.
  20. Yu YY, Teerlink CC, Fletcher (2011). Heritability of facial appearance.
  21. Deborah Neklason, Michelle Done, Nykole Sargent, Matthew Bailey, Craig Teerlink, Richard Kerber, Randall Bur (2012). Gap in the Middle of Familial Colorectal Cancer ¿ Moderately Penetrant Genetic Variants.
  22. Tashjian R, Teerlink CC, Farnham JM, Cannon-Albright L (2013). Genome Wide Association Study Identifying Genetic Risk for Full-Thickness Rotator Cuff Tears.
  23. Cannon-Albright LA, Farnham JM, Thai KK, Zone JJ, Teerlink C (2014). Significant evidence for linkage of cutaneous malignant melanoma to 1q41.
  24. Teerlink CC, Farnham JM, Cannon-Albright LA, Tashjian (2014). Genomewide association for rotator cuff disease identifies two significant SNPs.
  25. Farnham JM, Thai KK, Teerlink CC, Cannon-Albright LA (2014). Confirmation of association between melanoma and variants at a locus on 10q25.
  26. Agarwal N, Buckley TH, Farnham JM, Patel SB, Alex A, Teerlink C, Albright FS, Stephenson RA, Cannon-Albright LA (2014). Germ line predictors of response to androgen deprivation therapy in men with advanced prostate cancer.
  27. Cannon-Albright LA, Teerlink CC, Alex A, Albright FS, Stephenson RA, Agarwal (2014). A genomewide linkage study of lethal prostate cancer predisposition gene in a set of high-risk pedigrees.
  28. Agarwal N, Heemers H, Farnham JM, Patel SB, Gill DM, Gupta S, Teerlink CC, Stephenson RA, Alex A, Cannon-Albright L (2016). Association of single nucleotide polymorphisms (SNPs) in TPD52 gene with response to treatment with enzalutamide (ENZA) in men with metastatic castration refractory prostate cancer (mCRPC). 168541,
  29. Teerlink CC, Huff C, Stevens J, Holmen SL, Trombetti K, Grossman D, Farnham JM, Wen J, Facelli JC, Meyer L, Zone JJ, Leachman S, Cannon-Albright LA (2017). A rare variant in GOLM1 predisposes to cutaneous malignant melanoma.
  30. Teerlink CC, Hahn AW, Farnham JM, Esther J, Rathi N, Agarwal N, Cannon Albright LA (2018). A genome-wide association study of metastatic prostate cancer.
  31. Youngwon Kim Y, Sharp SJ, Hwang S, Luo S, Yeung SLA, Teerlink CC (2019). Genetic Risk, Muscle Strength And Stroke Risk.

Other

  1. Tashjian RZ, Granger EK, Farnham JM, Cannon-Albright LA, Teerlink C (2016). Erratum to "Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms" [J Shoulder Elbow Surg 2016;25:174-179]. Journal of shoulder and elbow surgery, 25(10), 1731.
  2. Teerlink CC, Cannon-Albright LA, Tashjian R (2016). Erratum to "Significant association of full-thickness rotator cuff tears and estrogen-related receptor-beta (ESRRB)" [J Shoulder Elbow Surg 2015;24:e31-e35]. 25(5), 864.