Multiple Common Susceptibility Variants near BMP Pathway Loci GREM1, BMP4, and BMP2 Explain Part of the Missing Heritability of Colorectal Cancer IPM Tomlinson, LG Carvajal-Carmona, SE Dobbins, A Tenesa, AM Jones, ... PLoS genetics 7 (6), e1002105, 2011 | 240 | 2011 |
Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25 L Fejerman, N Ahmadiyeh, D Hu, S Huntsman, KB Beckman, JL Caswell, ... Nature communications 5 (1), 5260, 2014 | 146 | 2014 |
Germline mutations in PALB2, BRCA1, and RAD51C, which regulate DNA recombination repair, in patients with gastric cancer R Sahasrabudhe, P Lott, M Bohorquez, T Toal, AP Estrada, JJ Suarez, ... Gastroenterology 152 (5), 983-986. e6, 2017 | 117 | 2017 |
Five endometrial cancer risk loci identified through genome-wide association analysis THT Cheng, DJ Thompson, TA O'Mara, JN Painter, DM Glubb, S Flach, ... Nature genetics 48 (6), 667-674, 2016 | 92 | 2016 |
Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk JN Painter, TA O'mara, J Batra, T Cheng, FA Lose, J Dennis, ... Human molecular genetics 24 (5), 1478-1492, 2015 | 65 | 2015 |
A polygenic risk score for breast cancer in US Latinas and Latin American women Y Shieh, L Fejerman, PC Lott, K Marker, SD Sawyer, D Hu, S Huntsman, ... JNCI: Journal of the National Cancer Institute 112 (6), 590-598, 2020 | 64 | 2020 |
COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer IPM Tomlinson, M Dunlop, H Campbell, B Zanke, S Gallinger, T Hudson, ... British journal of cancer 102 (2), 447-454, 2010 | 64 | 2010 |
Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment P Villanueva, R Nudel, A Hoischen, MA Fernández, NH Simpson, ... PLoS genetics 11 (3), e1004925, 2015 | 57 | 2015 |
Clinical manifestations of colorectal cancer patients from a large multicenter study in Colombia M Bohorquez, R Sahasrabudhe, A Criollo, MC Sanabria-Salas, A Velez, ... Medicine 95 (40), e4883, 2016 | 54 | 2016 |
The HABP2 G534E Variant Is an Unlikely Cause of Familial Nonmedullary Thyroid Cancer R Sahasrabudhe, J Stultz, J Williamson, P Lott, A Estrada, M Bohorquez, ... The journal of clinical endocrinology & metabolism 101 (3), 1098-1103, 2016 | 47 | 2016 |
Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1 THT Cheng, D Thompson, J Painter, T O’Mara, M Gorman, L Martin, ... Scientific reports 5 (1), 17369, 2015 | 43 | 2015 |
Identification of novel common breast cancer risk variants at the 6q25 locus among Latinas J Hoffman, L Fejerman, D Hu, S Huntsman, M Li, EM John, G Torres-Mejia, ... Breast Cancer Research 21, 1-12, 2019 | 42 | 2019 |
COGENT (COlorectal cancer GENeTics) revisited RS Houlston, Members of COGENT Mutagenesis 27 (2), 143-151, 2012 | 37 | 2012 |
Human epidermal growth factor receptor 2–positive breast cancer is associated with indigenous American ancestry in Latin American women KM Marker, VA Zavala, T Vidaurre, PC Lott, JN Vásquez, ... Cancer research 80 (9), 1893-1901, 2020 | 31 | 2020 |
A snapshot of current genetic testing practice in Lynch syndrome: The results of a representative survey of 33 Latin American existing centres/registries A Della Valle, BM Rossi, EI Palmero, M Antelo, CA Vaccaro, ... European Journal of Cancer 119, 112-121, 2019 | 20 | 2019 |
Native American gene continuity to the modern admixed population from the Colombian Andes: implication for biomedical, population and forensic studies AA Criollo-Rayo, M Bohórquez, R Prieto, K Howarth, C Culma, ... Forensic Science International: Genetics 36, e1-e7, 2018 | 19 | 2018 |
Caracterización de los hallazgos histopatológicos de tumores colorrectales en pacientes del Tolima, Colombia NY Flórez-Delgado, ME Bohórquez, G Mateus, R Prieto Sánchez, ... Revista colombiana de Gastroenterología 27 (2), 88-95, 2012 | 19 | 2012 |
Novel MLH1 duplication identified in Colombian families with Lynch syndrome V Alonso-Espinaco, MD Giráldez, C Trujillo, H van der Klift, J Muñoz, ... Genetics in medicine 13 (2), 155-160, 2011 | 18 | 2011 |
The 8q24 rs6983267G variant is associated with increased thyroid cancer risk R Sahasrabudhe, A Estrada, P Lott, L Martin, GP Echeverry, A Velez, ... Endocrine-related cancer 22 (5), 841-849, 2015 | 17 | 2015 |
BRAF and TERT mutations in papillary thyroid cancer patients of Latino ancestry AP Estrada-Flórez, ME Bohórquez, A Vélez, CS Duque, JH Donado, ... Endocrine connections 8 (9), 1310-1317, 2019 | 16 | 2019 |