Craig Teerlink

Craig Teerlink, PhD

Languages spoken: English

Academic Information

Departments Primary - Internal Medicine

Divisions: Epidemiology , Public Health

Craig Teerlink, PhD, is a Research Associate Professor in the Division of Epidemiology in the Department of Medicine. In this role, he performs research for gene discovery in a variety of complex diseases.

Dr. Teerlink’s research has relied heavily on analysis of biobank datasets, in particular, the VA's Million Veterans Program dataset. His research has covered a range of activities contributing to gene discovery including GWAS techniques for common variant discovery and analysis of whole genome sequence data for rare variant discovery.

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

Education History

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

Selected Publications

Journal Article

  1. Candelieri-Surette D, Cheranda N, Lee J, Teerlink CC, Pimentel C, Lynch JA, Berlowitz D, Schoen MW (2025). The Impact of Race on Survival and Treatment in Veterans Treated for Metastatic Castration-Resistant Prostate Cancer. J Natl Compr Canc Netw, 23(12), 507-515.
  2. Crawford TB, Nelson T, Karunamuni R, Desai H, Hausler R, Teerlink C, Carter H, Pagadala MS, Alba PR, DuVall SL, Danowski ME, Brunette CA, Ratner D, Garraway IP, Rose BS, Smith JR, Cooney KA, Vassy JL, Hauger RL, Lynch JA, Seibert TM, Maxwell KN (2025). Association of HOXB13 G84E with prostate cancer among 592,158 men. J Natl Compr Canc Netw, 23(10), e257055.
  3. Teerlink CC, Davis SM, Liu A, Lapato DM, Gorman B, Genovese G, Singh M, Reeve MP, Elswick A, Gentry E, Donner KM, Sipil TP, Ghazal A, Pagadala MS, Panizzon MS, Lancaster EE, FinnGen, banner authorship UKB working group authorship, Chatzinakos C, Ganna A, Bigdeli TB, Daly MJ, Lynch JA, Ross J, Peterson RE, Hauger RL Joint first authors (2025). Phenome-wide association study of male and female sex chromosome trisomies in 1.5 million participants of MVP, FinnGen, and UK Biobank. Am J Hum Genet, 112(9), 2088-2021.
  4. Candelieri-Surette D, Lee J, Lynch JA, Chang NN, Nelson TJ, Teerlink CC, Pimentel C, Schoen MW, Berlowitz D (2025). Epidemiology of Metastatic Castration-Resistant Prostate Cancer in Veterans Nationwide. J Natl Compr Canc Netw, 23(8), 307-313.
  5. Tuteja S, OBrien WJ, Ferraro JP, Damrauer SM, Itani K, Voight B, Teerlink CC, Lynch JA, DuVall SL, Strebel T, Kim MJ, Wilson MA, Barrett TW, Million Veteran Program (2025). Drug-gene interactions and clinical outcomes after vascular surgery in the Million Veteran Program. JAMA Surg, 160(7), 804-813.
  6. Pagadala MS, Teerlink CC, Jasuja GK, Palnati M, Anglin-Foote T, Chang NN, Deka R, Lee KM, Agiri FY, Amariuta T, Seibert TM, Rose BS, Pridgen KM, Lynch JA, Carter HK, Panizzon MS, Hauger RL (2025). Discovery of novel ancestry specific genes for androgens and hypogonadism in Million Veteran Program Men. Nat Commun, 16(1), 4104.
  7. 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 KM (2024). Clinical and Genetic Risk Factors for Progressive Fibrosis in Metabolic Dysfunction-Associated Steatotic Liver Disease. Hepatol Commun, 8(7), e0487.
  8. Tashjian RZ, Jurynec MJ, Christy K, Stevens J, Teerlink CC, Cannon-Albright LA, Allen-Brady K (2024). Identification of Rare Genetic Variants for Rotator Cuff Tearing and Repair in High-Risk Pedigrees. JSES Int.
  9. 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 Netw Open, 7(3), e242976.
  10. Davis SM, Teerlink C, Lynch JA, Gorman BR, Pagadala M, Liu A, Panizzon MS, Merritt VC, Genovese G, Ross JL, Hauger RL (2024). Prevalence, Morbidity, and Mortality of Men With Sex Chromosome Aneuploidy in the Million Veteran Program Cohort. JAMA Netw Open, 7(3), e244113.
  11. Davis SM, Teerlink CC, Lynch JA, Klamut N, Gorman BR, Pagadala M, Panizzon MS, Merritt VC, Genovese G, Pyarajan S, Ross JL, Hauger RL (2024). An Extra X Chromosome Among Adult Women in the Million Veteran Program: A More Benign Perspective of Trisomy X. Am J Med Genet C Semin Med Genet.
  12. Ochs-Balcom HM, Preus L, Du Z, Elston RC, Teerlink CC, Jia G, Guo X, Cai Q, Long J, Ping J, Li B, Stram DO, Shu XO, Sanderson M, Gao G, Ahearn T, Lunetta KL, Zirpoli G, Troester MA, Ruiz-Narvez EA, Haddad SA, Figueroa J, John EM, Bernstein L, Hu JJ, Ziegler RG, Nyante S, Bandera EV, Ingles SA, Mancuso N, Press MF, Deming SL, Rodriguez-Gil JL, Yao S, Ogundiran TO, Ojengbede O, Bolla MK, Dennis J, Dunning AM, Easton DF, Michailidou K, Pharoah PDP, Sandler DP, Taylor JA, Wang Q, OBrien KM, Weinberg CR, Kitahara CM, Blot W, Nathanson KL, Hennis A, Nemesure B, Ambs S, Sucheston-Campbell LE, Bensen JT, Chanock SJ, Olshan AF, Ambrosone CB, Olopade OI, The Ghana Breast Health Study Team, Conti DV, Palmer J, Garca-Closas M, Huo D, Zheng W, Haiman C (2024). Novel breast cancer susceptibility loci under linkage peaks identified in African ancestry consortia. Hum Mol Genet, 33(8), 687-697.
  13. 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 JA (2024). Genetic risk and likelihood of prostate cancer detection on first biopsy by ancestry. J Natl Cancer Inst, djae002.
  14. Cannon-Albright LA, Stevens J, Teerlink CC, Facelli JC, Allen-Brady K, Welm AL (2023). A rare variant in MDH2 (rs111879470) is associated with predisposition to recurrent breast cancer in an extended high-risk pedigree. Cancers (Basel), 15(24), 5851.
  15. 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 JE (2023). Germline EGFR mutations and familial lung cancer. J Clin Oncol, 41(34).
  16. 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 W (2023). A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall-cell lung cancer. . Int J Cancer, 15(153), 364-372.
  17. 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 H (2023). Autoimmune alleles at the major histocompatibility locus modify melanoma susceptibility. Am J Hum Genet, 13(S0002-9297), 00170-2.
  18. 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 (Basel), 15(7), 2085.
  19. Lisa A Cannon-Albright, Craig C Teerlink, Jeff Stevens, Franklin Huang, Csilla Sipeky, Johanna Schleutker, Rolando Hernandez, Julio Facelli, Neeraj Agarwal, Donald L Trump (2023). A rare variant in ERF (rs144812092) predisposes to prostate and bladder cancers. Cancers (Basel), 13(10), 2399.
  20. Teerlink CC, Miller JB, Vance EL, Staley LA, Stevens J, Tavana JP, Cloward ME, Page ML, Dayton L Alzheimers 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.
  21. 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. Int J Environ Res Public Health, 19(24), 16419.
  22. 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.
  23. 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. J Bone Joint Surg Am, 104(9), 774-779.
  24. Teerlink CC, Ward E, Miller JB, Staley LA, Stevens J, Tavana JP, Cloward M, Page M, Dayton L, Alzheimers Disease Genetics Consortium, Cannon-Albright LA, Kauwe JSK (2022). Analysis of high-risk pedigrees identifies twelve candidate variants for Alzheimer’s Disease. Alzheimers Dement, 18(2), 307-317.
  25. Teerlink CC, Stevens J, Hernandez R, Facelli J, Cannon-Albright LA (2021). An intronic variant in the CELF4 gene is associated with risk for colorectal cancer. Hum Mutat, 72, 101941.
  26. Kim Y, Sharp SJ, Hwang S, Luo S, Au Yeung SL, Teerlink CC (2021). Genetic risk, muscle strength and incident stroke: findings from the UK Biobank study. Mayo Clin Proc, 96(7), 1746-1757.
  27. CannonAlbright LA, Teerlink CC, Stevens J, Snow AK, Thompson BA, Bell R, Nguyen KN, Sargent NR, Kohlmann WK, Neklason DW, Tavtigian SV (2020). FANCM c5791CT stopgain mutation (rs144567652) is a familial colorectal cancer risk factor. Mol Genet Genomic Med, 8, e1532.
  28. 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.
  29. Tashjian R, Kim SK, Roche MD, Jones KB, Teerlink CC (2020). Genetic Variants Associated With Rotator Cuff Tearing Utilizing Multiple Population-Based Genetic Resources. J Shoulder Elbow Surg.
  30. 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 SV (2020). A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposis. Clin Genet, 97(6), 943-944.
  31. Cannon-Albright LA, Foster NL, Schliep K, Farnham JM, Teerlink CC, Kaddas H, Tschanz J, Corcoran C, Kauwe JSK (2019). Relative risk for Alzheimer disease based on complete family history. Neurology, 92(15), e1745-e1753.
  32. 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, Alzheimers Disease Sequencing Project (2019). Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry. JAMA Netw Open, 2(3), e191350.
  33. 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 LA (2018). A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant Melanoma. J Natl Cancer Inst, 110(12), 1380-1385.
  34. Teerlink CC, Bernhisel R, Cannon-Albright LA, Rollins MD (2018). A genealogical assessment of familial clustering of anorectal malformations. J Hum Genet, 63(10), 1029-1034.
  35. Cannon-Albright LA, Dintelman S, Maness T, Cerny J, Thomas A, Backus S, Farnham JM, Teerlink CC, Contreras J, Kauwe JSK, Meyer LJ (2018). Population genealogy resource shows evidence of familial clustering for Alzheimer disease. Neurol Genet, 4(4), e249.
  36. Potrony M, Puig-Butille JA, Farnham JM, Gimnez-Xavier P, Badenas C, Tell-Mart G, Aguilera P, Carrera C, Malvehy J, Teerlink CC, Puig S (2018). Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q. Eur J Hum Genet, 26(8), 1188-1193.
  37. Spiker WR, Brodke DS, Goz V, Lawrence B, Teerlink CC, Cannon-Albright LA (2018). Evidence of an Inherited Predisposition for Spinal Cord Tumors. Global Spine J, 8(4), 340-344.
  38. 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. Neurol Genet.
  39. Abbott D, Brockmeyer D, Neklason DW, Teerlink C, Cannon-Albright LA (2017). Population-based description of familial clustering of Chiari malformation Type I. J Neurosurg, 128(2), 460-465.
  40. 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, Alzheimers Disease Neuroimaging Initiative (2018). Correction to: Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience. Genome Med, 10(1), 4.
  41. 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 DJ (2017). gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels. Genet Epidemiol, 41(4), 297-308.
  42. 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.
  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, Hgdall 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, Hgdall 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, Lubiski J, Stanford JL, Bentez 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, Aittomki 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, Gunel 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, Kjr SK, Pejovic T, Tammela TL, GENICA Network, PRACTICAL consortium, Drk T, Brning 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 D (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 Discov, 6(9), 1052-67.
  44. 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 L (2016). Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21. Hum Genet, 135(8), 923-38.
  45. Tashjian RZ, Granger EK, Zhang Y, Teerlink CC, Cannon-Albright LA (2016). Identification of a genetic variant associated with rotator cuff repair healing. J Shoulder Elbow Surg, 25(6), 865-72.
  46. Tashjian RZ, Farnham JM, Granger EK, Teerlink CC, Cannon-Albright LA (2016). Evidence for an Environmental and Inherited Predisposition Contributing to the Risk for Global Tendinopathies or Compression Neuropathies in Patients With Rotator Cuff Tears. Orthop J Sports Med, 4(4), 2325967116642173.
  47. 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, Lindstrm 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 B (2016). Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation. Nat Commun, 7, 10979.
  48. Tashjian RZ, Granger EK, Farnham JM, Cannon-Albright LA, Teerlink CC (2015). Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms. J Shoulder Elbow Surg, 25(2), 174-9.
  49. Albright F, Stephenson RA, Agarwal N, Teerlink CC, Lowrance WT, Farnham JM, Albright LA (2015). Prostate cancer risk prediction based on complete prostate cancer family history. Prostate, 75(4), 390-8.
  50. Teerlink CC, Cannon-Albright LA, Tashjian RZ (2015). Significant association of full-thickness rotator cuff tears and estrogen-related receptor-β (ESRRB). J Shoulder Elbow Surg, 24(2), e31-5.
  51. Teerlink CC, Lisa A Cannon-Albright LA, Tashjian R (06/27/2014). Significant Association of Full-Thickness Rotator Cuff Tears and ESRRB (Estrogen-related Receptor Beta). J Shoulder Elbow Surg.
  52. Cannon-Albright LA, Farnham JM, Bailey M, Albright FS, Teerlink CC, Agarwal N, Stephenson RA, Thomas A (2014). Identification of specific Y chromosomes associated with increased prostate cancer risk. Prostate, 74(9), 991-8.
  53. 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, Grnberg 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 LA (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. Hum Genet, 133(3), 347-56.
  54. Teerlink C, Nelson Q, Burt R, Cannon-Albright L (2014). Significant evidence of linkage for a gene predisposing to colorectal cancer and multiple primary cancers on 22q11. Clin Transl Gastroenterol, 5, e50.
  55. 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.
  56. 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, OBrien 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.
  57. 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 WB (2013). HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG). Hum Genet, 132(1), 5-14.
  58. Cannon-Albright LA, Teerlink CC, Farnham JM, Thomas AW, Zone JJ, Leachman SA (2013). Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21. J Invest Dermatol, 133(1), 128-34.
  59. Cai Z, Thomas A, Teerlink C, Farnham JM, Cannon-Albright LA, Camp NJ (2012). Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees. BMC Genomics, 13, 676.
  60. 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 J (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). Hum Genet, 131(7), 1095-103.
  61. Albright F, Teerlink C, Werner TL, Cannon-Albright LA (2012). Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site. BMC Cancer, 12, 138.
  62. McCarthy JP, Browning WD, Teerlink C, Veit G (2012). Treatment of herpes labialis: comparison of two OTC drugs and untreated controls. J Esthet Restor Dent, 24(2), 103-9.
  63. Teerlink CC, Albright FS, Lins L, Cannon-Albright LA (2012). A comprehensive survey of cancer risks in extended families. Genet Med, 14(1), 107-14.
  64. Teerlink C, Farnham J, Allen-Brady K, Camp NJ, Thomas A, Leachman S, Cannon-Albright L (2012). A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. Hum Genet, 131(1), 77-85.
  65. Allen-Brady K, Cannon-Albright L, Farnham JM, Teerlink C, Vierhout ME, van Kempen LC, Kluivers KB, Norton PA (2011). Identification of six loci associated with pelvic organ prolapse using genome-wide association analysis. Obstet Gynecol, 118(6), 1345-53.
  66. Teerlink CC, Thomas A (2010). An application of the latent p value method to assess linkage in asthma pedigrees. Hum Hered, 70(1), 1-8.
  67. Tashjian RZ, Farnham JM, Albright FS, Teerlink CC, Cannon-Albright LA (2009). Evidence for an inherited predisposition contributing to the risk for rotator cuff disease. J Bone Joint Surg Am, 91(5), 1136-42.
  68. 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.
  69. Teerlink CC, Camp NJ, Bansal A, Crapo R, Hughes D, Kort E, Rowe K, Cannon-Albright LA (2009). Significant evidence for linkage to chromosome 5q13 in a genome-wide scan for asthma in an extended pedigree resource. Eur J Hum Genet, 17(5), 636-43.
  70. Teerlink CC, Hegewald MJ, Cannon-Albright LA (2007). A genealogical assessment of heritable predisposition to asthma mortality. Am J Respir Crit Care Med, 176(9), 865-70.
  71. Allen-Brady K, Horne BD, Malhotra A, Teerlink C, Camp NJ, Thomas A (2007). Analysis of high-density single-nucleotide polymorphism data: three novel methods that control for linkage disequilibrium between markers in a linkage analysis. BMC Proc, 1 Suppl 1, S160.

Abstract

  1. Youngwon Kim Y, Sharp SJ, Hwang S, Luo S, Yeung SLA, Teerlink CC (2019). Genetic Risk, Muscle Strength And Stroke Risk. [Abstract].
  2. 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 [Abstract]. GUASCO Conference 2019.
  3. 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 (Accepted). A rare variant in GOLM1 predisposes to cutaneous malignant melanoma [Abstract]. ASHG Conference 2017.
  4. Agarwal N, Heemers H, Farnham JM, Patel SB, Gill DM, Gupta S, Teerlink CC, Stephenson RA, Alex A, Cannon-Albright LA (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) [Abstract]. ASCO Conference, 168541.
  5. Neeraj Agarwal, Anitha Alex, James M Farnham, Shiven B Patel, Srinivas Kiran Tantravahi, Craig Teerlink, Frederick S Albright, Robert A Stephenson, Lisa A Cannon-Albright (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) [Abstract]. ASCO, No.150082.
  6. 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-Albright (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) [Abstract]. ASCO, No. 151027.
  7. 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. [Abstract].
  8. Cannon-Albright LA, Teerlink CC, Alex A, Albright FS, Stephenson RA, Agarwal N (2014). A genomewide linkage study of lethal prostate cancer predisposition gene in a set of high-risk pedigrees. [Abstract].
  9. Cannon-Albright LA, Farnham JM, Thai KK, Zone JJ, Teerlink CC (2014). Significant evidence for linkage of cutaneous malignant melanoma to 1q41 [Abstract].
  10. Teerlink CC, Farnham JM, Cannon-Albright LA, Tashjian R (2014). Genomewide association for rotator cuff disease identifies two significant SNPs [Abstract].
  11. Farnham JM, Thai KK, Teerlink CC, Cannon-Albright LA (2014). Confirmation of association between melanoma and variants at a locus on 10q25 [Abstract].
  12. 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 SN (2014). Statistical Tests for Co-Segregation of Genetic Variants with Disease in Pedigrees [Abstract]. American Society of Human Genetics Conference.
  13. Tashjian R, Teerlink CC, Farnham JM, Cannon-Albright LA (2013). Genome Wide Association Study Identifying Genetic Risk for Full-Thickness Rotator Cuff Tears [Abstract]. American Society of Human Genetics Conference.
  14. Teerlink CC, Farham JM, Tashjian R, Cannon-Albright LA (2013). Evidence for a genetic contribution to rotator cuff disease in a new population genealogy at the Veterans Administration [Abstract]. American Society of Human Genetics Conference.
  15. Cannon-Albright LA, Farnham JM, Teerlink CC, Stephenson RA (2013). Identification of Y chromosomes associated with risk for prostate cancer [Abstract]. American Society of Human Genetics Conference.
  16. Teerlink CC, Nelson QC, Neeraj Agarwal N, Stephenson RA, Cannon-Albright LA (2013). A population-based analysis of clustering identifies a strong genetic contribution to recurrent prostate cancer [Abstract]. International Genetic Epidemiology Society Conference.
  17. Neklason DW, Gilcrease GW, Sargent NR, Snow A, Teerlink C, M Bailey M, Burt RW (2013). Exome Sequencing of Family with Carcinoid Cancers [Abstract]. American Society of Human Genetics Conference.
  18. Neklason D, Done M, Sargent N, Bailey M, Teerlink C, Burt R (2013). Exome sequencing of affected individuals in large multigenerational colorectal cancer kindred [Abstract]. Advances in Genome Biology & Technology Conference.
  19. 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. [Abstract]. International Genetic Epidemiology Society Conference.
  20. 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 Genetics (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) [Abstract]. International Genetic Epidemiology Society Conference.
  21. Deborah Neklason, Michelle Done, Nykole Sargent, Matthew Bailey, Craig Teerlink, Richard Kerber, Randall Burt (2012). Gap in the Middle of Familial Colorectal Cancer – Moderately Penetrant Genetic Variants [Abstract]. Clinical Oncological Society of Australia Conference.
  22. Cannon-Albright LA, Dintelman S, Maness T, Thomas A, Teerlink C, Meyer L (2012). A national resource for aging research: the Veterans Administration genealogy project [Abstract]. University of Utah Geriatrics Conference.
  23. Yu YY, Teerlink CC, Fletcher T (2011). Heritability of facial appearance [Abstract]. University of Utah Scientific Computing and Imaging Institute SCIIX Conference.
  24. Teerlink CC, Farnham J, Cannon-Albright LA (2011). Significant confirmation of linkage to melanoma at 9q21 in an extended Utah pedigree [Abstract]. International Genetic Epidemiology Society Conference.
  25. Cannon-Albright LA, Teerlink CC, Agarwal N, Stephenson R (2011). Evidence for a strong genetic contribution to lethal prostate cancer [Abstract]. American Society of Human Genetics.
  26. Teerlink CC, Farnham J, Allen-Brady K, Horne BD, Camp NJ, Cannon-Albright LA (2010). Using publicly available control data for GWAS - a simple strategy for genetic matching [Abstract]. American Society of Human Genetics Conference.
  27. Teerlink CC, Cryer ME, Thomas A (2009). Interpreting the mod score statistic in a genomewide scan for asthma [Abstract]. International Genetic Epidemiology Society Conference.
  28. Albright F, Teerlink CC, Farnham J, Backus S, Cannon-Albright LA (2009). Reconstituting genealogical information from a multipurpose data resource [Abstract]. American Medical Informatics Association Conference.
  29. Teerlink CC, Thomas A (2008). An application of the latent p-value method to assess linkage in asthma pedigrees [Abstract]. International Genetic Epidemiology Society Conference.
  30. Teerlink CC, Camp NJ, Cannon-Albright LA (2006). Genome-wide linkage analysis for asthma predisposition loci in an extended pedigree resource [Abstract]. International Genetic Epidemiology Society Conference.
  31. Teerlink CC, Cannon-Albright LA (2006). A genealogical assessment of heritable predisposition to asthma mortality [Abstract]. American Society of Human Genetics Conference.

Other

  1. Tashjian RZ, Granger EK, Farnham JM, Cannon-Albright LA, Teerlink CC (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]. J Shoulder Elbow Surg (25(10), p. 1731). United States.
  2. Teerlink CC, Cannon-Albright LA, Tashjian RZ (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]. J Shoulder Elbow Surg (25(5), p. 864). United States.