| Year |
Citation |
Score |
| 2021 |
Lin WY, Fordham SE, Hungate E, Sunter NJ, Elstob C, Xu Y, Park C, Quante A, Strauch K, Gieger C, Skol A, Rahman T, Sucheston-Campbell L, Wang J, Hahn T, et al. Genome-wide association study identifies susceptibility loci for acute myeloid leukemia. Nature Communications. 12: 6233. PMID 34716350 DOI: 10.1038/s41467-021-26551-x |
0.334 |
|
| 2020 |
Oliva M, Muñoz-Aguirre M, Kim-Hellmuth S, Wucher V, Gewirtz ADH, Cotter DJ, Parsana P, Kasela S, Balliu B, Viñuela A, Castel SE, Mohammadi P, Aguet F, Zou Y, Khramtsova EA, ... Skol AD, et al. The impact of sex on gene expression across human tissues. Science (New York, N.Y.). 369. PMID 32913072 DOI: 10.1126/Science.Aba3066 |
0.337 |
|
| 2018 |
Crona DJ, Skol AD, Leppänen VM, Glubb DM, Etheridge AS, Hilliard E, Peña CE, Peterson YK, Klauber-DeMore N, Alitalo KK, Innocenti F. Genetic variants of VEGFA and FLT4 are determinants of survival in renal cell carcinoma patients treated with sorafenib. Cancer Research. PMID 30385613 DOI: 10.1158/0008-5472.Can-18-1089 |
0.427 |
|
| 2017 |
Clay-Gilmour AI, Hahn T, Preus LM, Onel K, Skol A, Hungate E, Zhu Q, Haiman CA, Stram DO, Pooler L, Sheng X, Yan L, Liu Q, Hu Q, Liu S, et al. Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex. Blood Advances. 1: 1717-1728. PMID 29296818 DOI: 10.1182/Bloodadvances.2017006023 |
0.375 |
|
| 2017 |
Hungate EA, Applebaum MA, Skol AD, Vaksman Z, Diamond M, McDaniel L, Volchenboum SL, Stranger BE, Maris JM, Diskin SJ, Onel K, Cohn SL. Evaluation of Genetic Predisposition for MYCN-Amplified Neuroblastoma. Journal of the National Cancer Institute. 109. PMID 29117357 DOI: 10.1093/Jnci/Djx093 |
0.434 |
|
| 2017 |
Hulur I, Skol AD, Gamazon ER, Cox NJ, Onel K. Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma. Plos One. 12: e0185730. PMID 28973033 DOI: 10.1371/Journal.Pone.0185730 |
0.384 |
|
| 2016 |
Skol AD, Sasaki MM, Onel K. The genetics of breast cancer risk in the post-genome era: thoughts on study design to move past BRCA and towards clinical relevance. Breast Cancer Research : Bcr. 18: 99. PMID 27716388 DOI: 10.1186/S13058-016-0759-4 |
0.316 |
|
| 2016 |
Hungate EA, Vora SR, Gamazon ER, Moriyama T, Best T, Hulur I, Lee Y, Evans TJ, Ellinghaus E, Stanulla M, Rudant J, Orsi L, Clavel J, Milne E, Scott RJ, ... ... Skol AD, et al. A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology. Nature Communications. 7: 10635. PMID 26868379 DOI: 10.1038/Ncomms10635 |
0.463 |
|
| 2015 |
Pinto N, Volchenboum SL, Skol AD, Rhodes L, Doan A, Fein-Levy C, Lipton JM, Cunningham JM, Onel K. Establishing a translational genomics infrastructure in pediatric cancer: the GREAT KIDS experience. Personalized Medicine. 12: 221-229. PMID 29771652 DOI: 10.2217/Pme.14.90 |
0.317 |
|
| 2015 |
Sasaki MM, Skol AD, Bao R, Rhodes LV, Chambers R, Vokes EE, Cohen EE, Onel K. Integrated Genomic Analysis Suggests MLL3 Is a Novel Candidate Susceptibility Gene for Familial Nasopharyngeal Carcinoma. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 26014803 DOI: 10.1158/1055-9965.Epi-15-0275 |
0.37 |
|
| 2015 |
Hulur I, Gamazon ER, Skol AD, Xicola RM, Llor X, Onel K, Ellis NA, Kupfer SS. Enrichment of inflammatory bowel disease and colorectal cancer risk variants in colon expression quantitative trait loci. Bmc Genomics. 16: 138. PMID 25766683 DOI: 10.1186/S12864-015-1292-Z |
0.439 |
|
| 2015 |
Kariuki SN, Ghodke-Puranik Y, Dorschner JM, Chrabot BS, Kelly JA, Tsao BP, Kimberly RP, Alarcón-Riquelme ME, Jacob CO, Criswell LA, Sivils KL, Langefeld CD, Harley JB, Skol AD, Niewold TB. Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus. Genes and Immunity. 16: 15-23. PMID 25338677 DOI: 10.1038/Gene.2014.57 |
0.412 |
|
| 2015 |
Kupfer SS, Hulur I, Gamazon E, Skol A, Llor X, Onel K, Ellis NA. Abstract 4582: Enrichment of colorectal cancer and inflammatory bowel disease risk variants in colon expression quantitative trait loci in African Americans Cancer Research. 75: 4582-4582. DOI: 10.1158/1538-7445.Am2015-4582 |
0.475 |
|
| 2014 |
Cozen W, Timofeeva MN, Li D, Diepstra A, Hazelett D, Delahaye-Sourdeix M, Edlund CK, Franke L, Rostgaard K, Van Den Berg DJ, Cortessis VK, Smedby KE, Glaser SL, Westra HJ, Robison LL, ... ... Skol AD, et al. A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus. Nature Communications. 5: 3856. PMID 24920014 DOI: 10.1038/Ncomms4856 |
0.447 |
|
| 2014 |
Kupfer SS, Skol AD, Hong E, Ludvik A, Kittles RA, Keku TO, Sandler RS, Ellis NA. Shared and independent colorectal cancer risk alleles in TGFβ-related genes in African and European Americans. Carcinogenesis. 35: 2025-30. PMID 24753543 DOI: 10.1093/Carcin/Bgu088 |
0.508 |
|
| 2014 |
Paré-Brunet L, Glubb D, Evans P, Berenguer-Llergo A, Etheridge AS, Skol AD, Di Rienzo A, Duan S, Gamazon ER, Innocenti F. Discovery and functional assessment of gene variants in the vascular endothelial growth factor pathway. Human Mutation. 35: 227-35. PMID 24186849 DOI: 10.1002/Humu.22475 |
0.354 |
|
| 2014 |
Hulur I, Skol A, Onel K. Abstract 1297: The heritability of melanoma differs between light- and dark-skinned individuals of European descent Cancer Research. 74: 1297-1297. DOI: 10.1158/1538-7445.Am2014-1297 |
0.362 |
|
| 2013 |
Applebaum MA, Skol A, Bond G, Onel K. Abstract 429: Damage-induced apoptosis in primary human lymphocytes is a genetic program modified by gender and age. Cancer Research. 73: 429-429. DOI: 10.1158/1538-7445.Am2013-429 |
0.313 |
|
| 2013 |
Sasaki MM, Skol AD, Pugh TJ, Meyerson M, Onel K. Abstract 4018: Whole exome sequencing analysis of familial Medulloblastoma. Cancer Research. 73: 4018-4018. DOI: 10.1158/1538-7445.Am2013-4018 |
0.378 |
|
| 2012 |
Koldobskaya Y, Ko K, Kumar AA, Agik S, Arrington J, Kariuki SN, Franek BS, Kumabe M, Utset TO, Jolly M, Skol AD, Niewold TB. Gene-expression-guided selection of candidate loci and molecular phenotype analyses enhance genetic discovery in systemic lupus erythematosus. Clinical & Developmental Immunology. 2012: 682018. PMID 22988468 DOI: 10.1155/2012/682018 |
0.489 |
|
| 2012 |
Stanhope SA, Skol AD. Improved minimum cost and maximum power two stage genome-wide association study designs. Plos One. 7: e42367. PMID 22970116 DOI: 10.1371/Journal.Pone.0042367 |
0.306 |
|
| 2012 |
Gamazon ER, Skol AD, Perera MA. The limits of genome-wide methods for pharmacogenomic testing. Pharmacogenetics and Genomics. 22: 261-72. PMID 22344246 DOI: 10.1097/Fpc.0B013E328350Ca5F |
0.375 |
|
| 2012 |
Cozen W, Li D, Best T, Van Den Berg DJ, Gourraud PA, Cortessis VK, Skol AD, Mack TM, Glaser SL, Weiss LM, Nathwani BN, Bhatia S, Schumacher FR, Edlund CK, Hwang AE, et al. A genome-wide meta-analysis of nodular sclerosing Hodgkin lymphoma identifies risk loci at 6p21.32. Blood. 119: 469-75. PMID 22086417 DOI: 10.1182/Blood-2011-03-343921 |
0.467 |
|
| 2011 |
Kupfer SS, Anderson JR, Ludvik AE, Hooker S, Skol A, Kittles RA, Keku TO, Sandler RS, Ruiz-Ponte C, Castellvi-Bel S, Castells A, Carracedo A, Ellis NA. Genetic associations in the vitamin D receptor and colorectal cancer in African Americans and Caucasians. Plos One. 6: e26123. PMID 22046258 DOI: 10.1371/Journal.Pone.0026123 |
0.402 |
|
| 2011 |
Cheng R, Abney M, Palmer AA, Skol AD. QTLRel: an R package for genome-wide association studies in which relatedness is a concern. Bmc Genetics. 12: 66. PMID 21794153 DOI: 10.1186/1471-2156-12-66 |
0.391 |
|
| 2011 |
Parker CC, Cheng R, Sokoloff G, Lim JE, Skol AD, Abney M, Palmer AA. Fine-mapping alleles for body weight in LG/J × SM/J F₂ and F(34) advanced intercross lines. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 22: 563-71. PMID 21761260 DOI: 10.1007/S00335-011-9349-Z |
0.328 |
|
| 2011 |
Onel K, Best T, Skol AD, Li D, Kirchhoff T, Yasui Y, Bhatia S, Strong LC, Domchek SM, Nathanson KL, Olopade O, Mack TM, Conti DV, Offit K, Cozen W, et al. Abstract 5092: Variants at 6q21 implicate PRDM1 in the etiology of therapy-induced second malignancies after Hodgkin's lymphoma Cancer Research. 71: 5092-5092. DOI: 10.1158/1538-7445.Am2011-5092 |
0.418 |
|
| 2010 |
Kariuki SN, Franek BS, Mikolaitis RA, Utset TO, Jolly M, Skol AD, Niewold TB. Promoter variant of PIK3C3 is associated with autoimmunity against Ro and Sm epitopes in African-American lupus patients. Journal of Biomedicine & Biotechnology. 2010: 826434. PMID 20671926 DOI: 10.1016/J.Clim.2010.03.166 |
0.317 |
|
| 2010 |
Kupfer SS, Anderson JR, Hooker S, Skol A, Kittles RA, Keku TO, Sandler RS, Ellis NA. Genetic heterogeneity in colorectal cancer associations between African and European americans. Gastroenterology. 139: 1677-85, 1685.e1-8. PMID 20659471 DOI: 10.1053/J.Gastro.2010.07.038 |
0.369 |
|
| 2010 |
Kariuki SN, Franek BS, Kumar AA, Arrington J, Mikolaitis RA, Utset TO, Jolly M, Crow MK, Skol AD, Niewold TB. Trait-stratified genome-wide association study identifies novel and diverse genetic associations with serologic and cytokine phenotypes in systemic lupus erythematosus. Arthritis Research & Therapy. 12: R151. PMID 20659327 DOI: 10.1016/J.Clim.2010.03.347 |
0.396 |
|
| 2010 |
Cheng R, Lim JE, Samocha KE, Sokoloff G, Abney M, Skol AD, Palmer AA. Genome-wide association studies and the problem of relatedness among advanced intercross lines and other highly recombinant populations. Genetics. 185: 1033-44. PMID 20439773 DOI: 10.1534/Genetics.110.116863 |
0.399 |
|
| 2010 |
Best T, Skol AD, Gamazon E, Onel K. A Functional Analysis of Variants Associated with Therapy-Induced Second Malignancies After Hodgkin Lymphoma Identified by a Genome-Wide Scan Blood. 116: 3892-3892. DOI: 10.1182/Blood.V116.21.3892.3892 |
0.479 |
|
| 2010 |
Cozen W, Li D, Best T, Berg DJVD, Skol A, Cortessis VK, Mack TM, Glaser SL, Schumacher F, Weiss L, Nathwani BN, Hwang A, Bhatia S, Strong LC, Robison LL, et al. A Meta-Analysis of Nodular Sclerosis Hodgkin Lymphoma Identifies Risk Loci at 6p21.32 Blood. 116: 2686-2686. DOI: 10.1182/Blood.V116.21.2686.2686 |
0.491 |
|
| 2010 |
Kupfer SS, Anderson JR, Hooker S, Skol A, Kittles RA, Keku TO, Sandler RS, Ellis NA. Abstract PR-4: Genetic heterogeneity in colorectal cancer associations in African Americans Cancer Epidemiology, Biomarkers & Prevention. 19. DOI: 10.1158/1055-9965.Disp-10-Pr-6 |
0.469 |
|
| 2009 |
Hamidovic A, Dlugos A, Skol A, Palmer AA, de Wit H. Evaluation of genetic variability in the dopamine receptor D2 in relation to behavioral inhibition and impulsivity/sensation seeking: an exploratory study with d-amphetamine in healthy participants. Experimental and Clinical Psychopharmacology. 17: 374-83. PMID 19968402 DOI: 10.1037/A0017840 |
0.395 |
|
| 2009 |
Kupfer SS, Torres JB, Hooker S, Anderson JR, Skol AD, Ellis NA, Kittles RA. Novel single nucleotide polymorphism associations with colorectal cancer on chromosome 8q24 in African and European Americans. Carcinogenesis. 30: 1353-7. PMID 19520795 DOI: 10.1093/Carcin/Bgp123 |
0.432 |
|
| 2009 |
Knight JA, Skol AD, Shinde A, Hastings D, Walgren RA, Shao J, Tennant TR, Banerjee M, Allan JM, Le Beau MM, Larson RA, Graubert TA, Cox NJ, Onel K. Genome-wide association study to identify novel loci associated with therapy-related myeloid leukemia susceptibility. Blood. 113: 5575-82. PMID 19299336 DOI: 10.1182/Blood-2008-10-183244 |
0.431 |
|
| 2009 |
Maheshwari M, Shi J, Badner JA, Skol A, Willour VL, Muzny DM, Wheeler DA, Gerald FR, Detera-Wadleigh S, McMahon FJ, Potash JB, Gershon ES, Liu C, Gibbs RA. Common and rare variants of DAOA in bipolar disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 960-6. PMID 19194963 DOI: 10.1002/Ajmg.B.30925 |
0.521 |
|
| 2007 |
Sabeti PC, Varilly P, Fry B, Lohmueller J, Hostetter E, Cotsapas C, Xie X, Byrne EH, McCarroll SA, Gaudet R, Schaffner SF, Lander ES, Frazer KA, Ballinger DG, ... ... Skol A, et al. Genome-wide detection and characterization of positive selection in human populations. Nature. 449: 913-8. PMID 17943131 DOI: 10.1038/Nature06250 |
0.46 |
|
| 2007 |
Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, Gibbs RA, Belmont JW, Boudreau A, Hardenbol P, Leal SM, Pasternak S, Wheeler DA, Willis TD, Yu F, ... ... Skol A, et al. A second generation human haplotype map of over 3.1 million SNPs. Nature. 449: 851-61. PMID 17943122 DOI: 10.1038/Nature06258 |
0.513 |
|
| 2007 |
Skol AD, Scott LJ, Abecasis GR, Boehnke M. Optimal designs for two-stage genome-wide association studies. Genetic Epidemiology. 31: 776-88. PMID 17549752 DOI: 10.1002/Gepi.20240 |
0.491 |
|
| 2007 |
Willer CJ, Bonnycastle LL, Conneely KN, Duren WL, Jackson AU, Scott LJ, Narisu N, Chines PS, Skol A, Stringham HM, Petrie J, Erdos MR, Swift AJ, Enloe ST, Sprau AG, et al. Screening of 134 single nucleotide polymorphisms (SNPs) previously associated with type 2 diabetes replicates association with 12 SNPs in nine genes. Diabetes. 56: 256-64. PMID 17192490 DOI: 10.2337/Db06-0461 |
0.72 |
|
| 2006 |
Skol AD, Scott LJ, Abecasis GR, Boehnke M. Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies. Nature Genetics. 38: 209-13. PMID 16415888 DOI: 10.1038/Ng1706 |
0.547 |
|
| 2006 |
Skol AD, Scott LJ, Abecasis GR, Boehnke M. Correction: Corrigendum: Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies Nature Genetics. 38: 390-390. DOI: 10.1038/Ng0306-390 |
0.518 |
|
| 2005 |
Faraone SV, Skol AD, Tsuang DW, Young KA, Haverstock SL, Prabhudesai S, Mena F, Menon AS, Leong L, Sautter F, Baldwin C, Bingham S, Weiss D, Collins J, Keith T, et al. Genome scan of schizophrenia families in a large Veterans Affairs Cooperative Study sample: evidence for linkage to 18p11.32 and for racial heterogeneity on chromosomes 6 and 14. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 139: 91-100. PMID 16152571 DOI: 10.1002/Ajmg.B.30213 |
0.546 |
|
| 2005 |
Skol AD, Xiao R, Boehnke M. An algorithm to construct genetically similar subsets of families with the use of self-reported ethnicity information. American Journal of Human Genetics. 77: 346-54. PMID 16080111 DOI: 10.1086/432961 |
0.482 |
|
| 2005 |
Mohlke KL, Skol AD, Scott LJ, Valle TT, Bergman RN, Tuomilehto J, Boehnke M, Collins FS. Evaluation of SLC2A10 (GLUT10) as a candidate gene for type 2 diabetes and related traits in Finns. Molecular Genetics and Metabolism. 85: 323-7. PMID 15936967 DOI: 10.1016/J.Ymgme.2005.04.011 |
0.538 |
|
| 2004 |
Silander K, Mohlke KL, Scott LJ, Peck EC, Hollstein P, Skol AD, Jackson AU, Deloukas P, Hunt S, Stavrides G, Chines PS, Erdos MR, Narisu N, Conneely KN, Li C, et al. Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes. Diabetes. 53: 1141-9. PMID 15047633 DOI: 10.2337/Diabetes.53.4.1141 |
0.698 |
|
| 2003 |
Skol AD, Young KA, Tsuang DW, Faraone SV, Haverstock SL, Bingham S, Prabhudesai S, Mena F, Menon AS, Yu CE, Rundell P, Pepple J, Sauter F, Baldwin C, Weiss D, et al. Modest evidence for linkage and possible confirmation of association between NOTCH4 and schizophrenia in a large Veterans Affairs Cooperative Study sample. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 118: 8-15. PMID 12627457 DOI: 10.1002/Ajmg.B.10055 |
0.593 |
|
| 2002 |
Faraone SV, Skol AD, Tsuang DW, Bingham S, Young KA, Prabhudesai S, Haverstock SL, Mena F, Menon AS, Bisset D, Pepple J, Sautter F, Baldwin C, Weiss D, Collins J, et al. Linkage of chromosome 13q32 to schizophrenia in a large veterans affairs cooperative study sample. American Journal of Medical Genetics. 114: 598-604. PMID 12210272 DOI: 10.1002/Ajmg.10601 |
0.527 |
|
| 2002 |
Douglas JA, Skol AD, Boehnke M. Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family data. American Journal of Human Genetics. 70: 487-95. PMID 11791214 DOI: 10.1086/338919 |
0.635 |
|
| 2001 |
Tsuang DW, Skol AD, Faraone SV, Bingham S, Young KA, Prabhudesai S, Haverstock SL, Mena F, Menon AS, Bisset D, Pepple J, Sauter F, Baldwin C, Weiss D, Collins J, et al. Examination of genetic linkage of chromosome 15 to schizophrenia in a large Veterans Affairs Cooperative Study sample. American Journal of Medical Genetics. 105: 662-8. PMID 11803512 DOI: 10.1002/Ajmg.1550 |
0.545 |
|
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