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C. Teerlink · SciRah

Researcher profile · Semantic Scholar

C. Teerlink

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C. Teerlink — researcher profile on SciRah

h-index: 29
Works: 103
Citations: 6,105

Most-cited papers

REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.
N. Ioannidis, J. Rothstein, V. Pejaver, S. Middha +37 more
2016American Journal of Human Genetics2,614 citations Open access
Semantic Scholar
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
R. Eeles, Ali Olama, S. Benlloch, E. Saunders +140 more
2013Nature Genetics585 citations Open access
Semantic Scholar
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
D. Conti, B. Darst, Lilit C. Moss, E. Saunders +227 more
2021Nature Genetics407 citations Open access
Semantic Scholar
HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG)
Jian-Feng Xu, E. Lange, Ling-Yi Lu, S. Zheng +46 more
2012Human Genetics204 citations Open access
Semantic Scholar
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping
R. Eeles, A. A. Al Olama, S. Benlloch, E. Saunders +139 more
2012192 citations
Semantic Scholar
Genome-wide Meta-analyses of Breast, Ovarian and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by At Least Two Cancer Types
S. Kar, J. Beesley, A. A. Al Olama, K. Michailidou +223 more
2016Cancer Discovery188 citations Open access
Semantic Scholar
A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease.
Ali Amin Al Olama, Z. Kote-Jarai, F. Schumacher, F. Wiklund +143 more
2013Human Molecular Genetics144 citations Open access
Semantic Scholar
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Anqi Wang, Jiayi Shen, Alex A. Rodriguez, E. Saunders +309 more
2023Nature Genetics136 citations Open access
Semantic Scholar
Prostate cancer risk prediction based on complete prostate cancer family history
Frederick S. Albright, R. Stephenson, N. Agarwal, C. Teerlink +3 more
2014The Prostate125 citations Open access
Semantic Scholar
Evidence for an inherited predisposition contributing to the risk for rotator cuff disease.
R. Tashjian, J. Farnham, Frederick S. Albright, C. Teerlink +1 more
2009Journal of Bone and Joint Surgery. American volume104 citations Open access
Semantic Scholar
Relative risk for Alzheimer disease based on complete family history
L. Cannon-Albright, N. Foster, K. Schliep, J. Farnham +5 more
2019Neurology90 citations Open access
Semantic Scholar
Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer’s disease resilience
P. Ridge, C. Karch, Simon Hsu, Ivan Arano +27 more
2017Genome Medicine76 citations Open access
Semantic Scholar
A comprehensive survey of cancer risks in extended families
C. Teerlink, Frederick S. Albright, Lauro Lins, L. Cannon-Albright
2012Genetics in Medicine67 citations Open access
Semantic Scholar
Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry
D. Patel, J. Mez, B. Vardarajan, Lyndsay A. Staley +17 more
2019JAMA Network Open59 citations Open access
Semantic Scholar
Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site
Frederick S. Albright, C. Teerlink, T. Werner, L. Cannon-Albright
2012BMC Cancer58 citations Open access
Semantic Scholar
Identification of Six Loci Associated With Pelvic Organ Prolapse Using Genome-Wide Association Analysis
K. Allen-Brady, L. Cannon-Albright, J. Farnham, C. Teerlink +4 more
2011Obstetrics and Gynecology54 citations Open access
Semantic Scholar
Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation
Alexander Gusev, Huwenbo Shi, Gleb Kichaev, M. Pomerantz +124 more
2016Nature Communications53 citations Open access
Semantic Scholar
Significant linkage evidence for a predisposition gene for pelvic floor disorders on chromosome 9q21.
K. Allen-Brady, P. Norton, J. Farnham, C. Teerlink +1 more
2009American Journal of Human Genetics53 citations Open access
Semantic Scholar
Significant association of full-thickness rotator cuff tears and estrogen-related receptor-β (ESRRB).
C. Teerlink, L. Cannon-Albright, R. Tashjian
2015Journal of shoulder and elbow surgery50 citations
Semantic Scholar
Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms.
R. Tashjian, Erin K. Granger, J. Farnham, L. Cannon-Albright +1 more
2016Journal of shoulder and elbow surgery47 citations
Semantic Scholar
Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer
D. Schaid, S. Mcdonnell, L. FitzGerald, L. Derycke +35 more
2020European Urology46 citations Open access
Semantic Scholar
Identification of a genetic variant associated with rotator cuff repair healing.
R. Tashjian, Erin K. Granger, Yue Zhang, C. Teerlink +1 more
2016Journal of shoulder and elbow surgery41 citations
Semantic Scholar
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21
C. Teerlink, D. Leongamornlert, Tokhir Dadaev, Alun Thomas +37 more
2016Human Genetics40 citations Open access
Semantic Scholar
Germline EGFR mutations and familial lung cancer
G. Oxnard, Ruthia Chen, Jennifer C Pharr, Diane R. Koeller +19 more
2023Journal of Clinical Oncology38 citations Open access
Semantic Scholar
Population-based description of familial clustering of Chiari malformation Type I.
D. Abbott, D. Brockmeyer, Deborah W. Neklason, C. Teerlink +1 more
2017Journal of Neurosurgery37 citations Open access
Semantic Scholar
A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q
C. Teerlink, J. Farnham, K. Allen-Brady, N. Camp +3 more
2011Human Genetics31 citations
Semantic Scholar
Genetic Risk, Muscle Strength, and Incident Stroke: Findings From the UK Biobank Study.
Youngwon Kim, Semi Hwang, S. Sharp, Shan Luo +2 more
2021Mayo Clinic proceedings30 citations Open access
Semantic Scholar
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
C. Teerlink, S. Thibodeau, S. Mcdonnell, D. Schaid +43 more
2013Human Genetics27 citations Open access
Semantic Scholar
Genetic Variants Associated With Rotator Cuff Tearing Utilizing Multiple Population-Based Genetic Resources.
R. Tashjian, Stuart K. Kim, Megan Roche, Kevin B. Jones +1 more
2020Journal of shoulder and elbow surgery25 citations
Semantic Scholar
A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant Melanoma
C. Teerlink, C. Huff, J. Stevens, Yao Yu +15 more
2018Journal of the National Cancer Institute24 citations Open access
Semantic Scholar
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)
G. Jin, Ling-Yi Lu, K. Cooney, Anna M. Ray +41 more
2011Human Genetics22 citations Open access
Semantic Scholar
The Effect of Sex Hormone Deficiency on the Incidence of Rotator Cuff Repair
Karch M. Smith, J. Hotaling, A. Presson, Chong Zhang +5 more
2022Journal of Bone and Joint Surgery. American volume21 citations
Semantic Scholar
A role for the MEGF6 gene in predisposition to osteoporosis
C. Teerlink, Michael J. Jurynec, Rolando Hernandez, J. Stevens +6 more
2020bioRxiv21 citations Open access
Semantic Scholar
Pathogenic Germline DNA Repair Gene and HOXB13 Mutations in Men With Metastatic Prostate Cancer.
J. Boyle, A. Hahn, A. Kapron, W. Kohlmann +8 more
2020JCO Precision Oncology19 citations Open access
Semantic Scholar
A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposis
B. Thompson, A. Snow, Cathryn Koptiuch, W. Kohlmann +9 more
2019bioRxiv18 citations Open access
Semantic Scholar
Analysis of high‐risk pedigrees identifies 11 candidate variants for Alzheimer's disease
C. Teerlink, Justin B. Miller, Elizabeth L Vance, Lyndsay A. Staley +7 more
2021Alzheimer's & Dementia16 citations Open access
Semantic Scholar
Identification of specific Y-chromosomes associated with increased prostate cancer risk
L. Cannon-Albright, J. Farnham, M. Bailey, Frederick S. Albright +4 more
2014The Prostate13 citations Open access
Semantic Scholar
Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21
L. Cannon-Albright, C. Teerlink, J. Farnham, Alun Thomas +2 more
2012Journal of Investigative Dermatology13 citations Open access
Semantic Scholar
Significant evidence for linkage to chromosome 5q13 in a genome-wide scan for asthma in an extended pedigree resource
C. Teerlink, N. Camp, A. Bansal, R. Crapo +4 more
2008European Journal of Human Genetics12 citations Open access
Semantic Scholar
Analysis of high-density single-nucleotide polymorphism data: three novel methods that control for linkage disequilibrium between markers in a linkage analysis
K. Allen-Brady, B. Horne, A. Malhotra, C. Teerlink +2 more
2007BMC Proceedings12 citations Open access
Semantic Scholar
Evidence for an Environmental and Inherited Predisposition Contributing to the Risk for Global Tendinopathies or Compression Neuropathies in Patients With Rotator Cuff Tears
R. Tashjian, J. Farnham, Erin K. Granger, C. Teerlink +1 more
2016Orthopaedic Journal of Sports Medicine11 citations Open access
Semantic Scholar
Erratum to "Significant association of full-thickness rotator cuff tears and estrogen-related receptor-β (ESRRB)" [J Shoulder Elbow Surg 2015;24:e31-e35].
C. Teerlink, L. Cannon-Albright, R. Tashjian
2016Journal of shoulder and elbow surgery11 citations
Semantic Scholar
Comorbidity and Cancer Disease Rates among Those at High-Risk for Alzheimer’s Disease: A Population Database Analysis
D. Valentine, C. Teerlink, J. Farnham, K. Rowe +4 more
2022International Journal of Environmental Research and Public Health9 citations Open access
Semantic Scholar
Identification and genomic analysis of pedigrees with exceptional longevity identifies candidate rare variants
Justin B. Miller, Elizabeth M. Ward, Lyndsay A. Staley, Jeffrey Stevens +7 more
2020Neurobiology of Disease9 citations Open access
Semantic Scholar
FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor
L. Cannon-Albright, C. Teerlink, Jeffrey Stevens, A. Snow +7 more
2020Molecular Genetics & Genomic Medicine8 citations Open access
Semantic Scholar
Population genealogy resource shows evidence of familial clustering for Alzheimer disease
L. Cannon-Albright, Sue M. Dintelman, T. Maness, J. Cerny +7 more
2018Neurology: Genetics8 citations Open access
Semantic Scholar
A genealogical assessment of familial clustering of anorectal malformations
C. Teerlink, R. Bernhisel, L. Cannon-Albright, M. Rollins
2018Journal of Human Genetics8 citations
Semantic Scholar
gsSKAT: Rapid Gene-Set Analysis and Multiple Testing Correction for Rare-variant Association Studies using Weighted Linear Kernels
Nicholas B. Larson, S. Mcdonnell, L. C. Albright, C. Teerlink +28 more
2017Genetic Epidemiology8 citations Open access
Semantic Scholar
An Extra X Chromosome Among Adult Women in the Million Veteran Program: A More Benign Perspective of Trisomy X
S. Davis, C. Teerlink, J. Lynch, Natalia Klamut +7 more
2024American Journal of Medical Genetics. Part C, Seminars in Medical Genetics7 citations Open access
Semantic Scholar
An intronic variant in the CELF4 gene is associated with risk for colorectal cancer
C. Teerlink, J. Stevens, Rolando Hernandez, J. Facelli +1 more
2021Cancer Epidemiology7 citations Open access
Semantic Scholar

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