| Year |
Citation |
Score |
| 2023 |
Astore C, Sharma S, Nagpal S, Cutler DJ, Rioux JD, Cho JH, McGovern DPB, Brant SR, Kugathasan S, Jordan IK, Gibson G. The role of admixture in the rare variant contribution to inflammatory bowel disease. Genome Medicine. 15: 97. PMID 37968638 DOI: 10.1186/s13073-023-01244-w |
0.388 |
|
| 2023 |
Curtis SW, Carlson JC, Beaty TH, Murray JC, Weinberg SM, Marazita ML, Cotney JL, Cutler DJ, Epstein MP, Leslie EJ. Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes. Human Genetics. PMID 37676273 DOI: 10.1007/s00439-023-02596-4 |
0.312 |
|
| 2023 |
Curtis SW, Carlson JC, Beaty TH, Murray JC, Weinberg SM, Marazita ML, Cotney JL, Cutler DJ, Epstein MP, Leslie EJ. Rare genetic variants in modify orofacial cleft phenotypes. Medrxiv : the Preprint Server For Health Sciences. PMID 37034635 DOI: 10.1101/2023.03.24.23287714 |
0.303 |
|
| 2022 |
Sazonovs A, Stevens CR, Venkataraman GR, Yuan K, Avila B, Abreu MT, Ahmad T, Allez M, Ananthakrishnan AN, Atzmon G, Baras A, Barrett JC, Barzilai N, Beaugerie L, Beecham A, ... ... Cutler DJ, et al. Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility. Nature Genetics. PMID 36038634 DOI: 10.1038/s41588-022-01156-2 |
0.708 |
|
| 2022 |
Kozlova A, Zhang S, Kotlar AV, Jamison B, Zhang H, Shi S, Forrest MP, McDaid J, Cutler DJ, Epstein MP, Zwick ME, Pang ZP, Sanders AR, Warren ST, Gejman PV, et al. Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons. American Journal of Human Genetics. 109: 1500-1519. PMID 35931052 DOI: 10.1016/j.ajhg.2022.07.001 |
0.589 |
|
| 2022 |
Badshah N, Mattison KA, Ahmad S, Chopra P, Johnston HR, Ahmad S, Khan SH, Sarwar MT, Cutler DJ, Taylor M, Vadlamani G, Zwick ME, Escayg A. Novel Missense Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior. Frontiers in Neurology. 13: 918022. PMID 35911904 DOI: 10.3389/fneur.2022.918022 |
0.624 |
|
| 2022 |
Kong HE, Lim J, Linsalata A, Kang Y, Malik I, Allen EG, Cao Y, Shubeck L, Johnston R, Huang Y, Gu Y, Guo X, Zwick ME, Qin Z, Wingo TS, ... ... Cutler DJ, et al. Identification of as a genetic modifier of fragile X-associated tremor/ataxia syndrome. Proceedings of the National Academy of Sciences of the United States of America. 119: e2118124119. PMID 35617426 DOI: 10.1073/pnas.2118124119 |
0.614 |
|
| 2022 |
Jurickova I, Bonkowski E, Angerman E, Novak E, Huron A, Akers G, Iwasawa K, Braun T, Hadar R, Hooker M, Han S, Cutler DJ, Okou DT, Kugathasan S, Jegga A, et al. Eicosatetraynoic Acid and Butyrate Regulate Human Intestinal Organoid Mitochondrial and Extracellular Matrix Pathways Implicated in Crohn's Disease Strictures. Inflammatory Bowel Diseases. PMID 35259271 DOI: 10.1093/ibd/izac037 |
0.656 |
|
| 2022 |
Venkateswaran S, Somineni HK, Kilaru V, Katrinli S, Prince J, Okou DT, Hyams JS, Denson LA, Kellermayer R, Gibson G, Cutler DJ, Smith AK, Kugathasan S, Conneely KN. Methylation Quantitative Trait Loci are Largely Consistent across Disease States in Crohn's disease. G3 (Bethesda, Md.). PMID 35172000 DOI: 10.1093/g3journal/jkac041 |
0.719 |
|
| 2021 |
Trevino CE, Holleman AM, Corbitt H, Maslen CL, Rosser TC, Cutler DJ, Johnston HR, Rambo-Martin BL, Oberoi J, Dooley KJ, Capone GT, Reeves RH, Cordell HJ, Keavney BD, Agopian AJ, et al. Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome. Scientific Reports. 11: 15164. PMID 34285246 DOI: 10.1038/s41598-021-94021-x |
0.565 |
|
| 2021 |
Mosley TJ, Johnston HR, Cutler DJ, Zwick ME, Mulle JG. Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders. Bmc Medical Genomics. 14: 154. PMID 34107974 DOI: 10.1186/s12920-021-00999-8 |
0.612 |
|
| 2021 |
Somineni HK, Weitzner JH, Venkateswaran S, Dodd A, Prince J, Karikaran A, Sauer CG, Abramowicz S, Zwick ME, Cutler DJ, Okou DT, Chopra P, Kugathasan S. Site- and Taxa-Specific Disease-Associated Oral Microbial Structures Distinguish Inflammatory Bowel Diseases. Inflammatory Bowel Diseases. PMID 34002220 DOI: 10.1093/ibd/izab082 |
0.763 |
|
| 2021 |
Somineni HK, Nagpal S, Venkateswaran S, Cutler DJ, Okou DT, Haritunians T, Simpson CL, Begum F, Datta LW, Quiros AJ, Seminerio J, Mengesha E, Alexander JS, Baldassano RN, Dudley-Brown S, et al. Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease. American Journal of Human Genetics. PMID 33600772 DOI: 10.1016/j.ajhg.2021.02.001 |
0.806 |
|
| 2020 |
Trevino CE, Holleman AM, Corbitt H, Maslen CL, Rosser TC, Cutler DJ, Johnston HR, Rambo-Martin BL, Oberoi J, Dooley KJ, Capone GT, Reeves RH, Cordell HJ, Keavney BD, Agopian AJ, et al. Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome. Scientific Reports. 10: 18051. PMID 33093519 DOI: 10.1038/s41598-020-74650-4 |
0.649 |
|
| 2020 |
Bishop MR, Diaz Perez KK, Sun M, Ho S, Chopra P, Mukhopadhyay N, Hetmanski JB, Taub MA, Moreno-Uribe LM, Valencia-Ramirez LC, Restrepo Muñeton CP, Wehby G, Hecht JT, Deleyiannis F, Weinberg SM, ... ... Cutler DJ, et al. Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios. American Journal of Human Genetics. PMID 32574564 DOI: 10.1016/J.Ajhg.2020.05.018 |
0.384 |
|
| 2020 |
Cleynen I, Engchuan W, Hestand MS, Heung T, Holleman AM, Johnston HR, Monfeuga T, McDonald-McGinn DM, Gur RE, Morrow BE, Swillen A, Vorstman JAS, Bearden CE, Chow EWC, van den Bree M, ... ... Cutler DJ, et al. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry. PMID 32015465 DOI: 10.1038/S41380-020-0654-3 |
0.6 |
|
| 2020 |
Satterstrom FK, Kosmicki JA, Wang J, Breen MS, De Rubeis S, An JY, Peng M, Collins R, Grove J, Klei L, Stevens C, Reichert J, Mulhern MS, Artomov M, Gerges S, ... ... Cutler DJ, et al. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism. Cell. PMID 31981491 DOI: 10.1016/J.Cell.2019.12.036 |
0.635 |
|
| 2020 |
Venkateswaran S, Somineni HK, Matthews J, Kilaru V, Denson LA, Hyams JS, Investigators P, Cutler DJ, Smith AK, Conneely KN, Kugathasan S. 614 RECTAL TISSUE DNA METHYLATION IN ULCERATIVE COLITIS SHOWS DISEASE-SPECIFIC ASSOCIATIONS: INSIGHTS FROM LONGITUDINAL ANALYSIS OF PROTECT STUDY PARTICIPANTS Gastroenterology. 158: S-131. DOI: 10.1016/S0016-5085(20)31007-6 |
0.307 |
|
| 2020 |
Niklinska-Schirtz BJ, Matthews J, Venkateswaran S, Prince J, Dodd A, Cutler DJ, Kugathasan S. 589 Pediatric Crohn'S Disease Patient Derived Organoids Show Persistent Transcriptomic Epithelial Cell Defects Gastroenterology. 158. DOI: 10.1016/S0016-5085(20)30995-1 |
0.33 |
|
| 2019 |
Solis-Lemus CR, Fischer ST, Todor A, Liu C, Leslie EJ, Cutler DJ, Ghosh D, Epstein MP. Leveraging Family History in Case-Control Analyses of Rare Variation. Genetics. PMID 31843756 DOI: 10.1534/Genetics.119.302846 |
0.323 |
|
| 2019 |
Venkateswaran S, Denson LA, Jurickova I, Dodd A, Zwick ME, Cutler DJ, Kugathasan S, Okou DT. Neutrophil GM-CSF signaling in inflammatory bowel disease patients is influenced by non-coding genetic variants. Scientific Reports. 9: 9168. PMID 31235766 DOI: 10.1038/S41598-019-45701-2 |
0.786 |
|
| 2019 |
Doan RN, Lim ET, De Rubeis S, Betancur C, Cutler DJ, Chiocchetti AG, Overman LM, Soucy A, Goetze S, Freitag CM, Daly MJ, Walsh CA, Buxbaum JD, Yu TW. Recessive gene disruptions in autism spectrum disorder. Nature Genetics. PMID 31209396 DOI: 10.1038/S41588-019-0433-8 |
0.352 |
|
| 2019 |
Wingo TS, Cutler DJ, Wingo AP, Le NA, Rabinovici GD, Miller BL, Lah JJ, Levey AI. Association of Early-Onset Alzheimer Disease With Elevated Low-density Lipoprotein Cholesterol Levels and Rare Genetic Coding Variants of APOB. Jama Neurology. PMID 31135820 DOI: 10.1001/Jamaneurol.2019.0648 |
0.313 |
|
| 2019 |
Somineni HK, Venkateswaran S, Kilaru V, Marigorta UM, Mo A, Okou DT, Kellermayer R, Mondal K, Cobb D, Walters TD, Griffiths A, Noe JD, Crandall WV, Rosh JR, Mack DR, ... ... Cutler DJ, et al. Blood-derived DNA Methylation Signatures of Crohn's Disease and Severity of Intestinal Inflammation. Gastroenterology. PMID 30779925 DOI: 10.1053/J.Gastro.2019.01.270 |
0.702 |
|
| 2019 |
Berauer JP, Mezina AI, Okou DT, Sabo A, Muzny DM, Gibbs RA, Hegde MR, Chopra P, Cutler DJ, Perlmutter DH, Bull LN, Thompson RJ, Loomes KM, Spinner NB, Rajagopalan R, et al. Identification of PKD1L1 Gene Variants in Children with the Biliary Atresia Splenic Malformation Syndrome. Hepatology (Baltimore, Md.). PMID 30664273 DOI: 10.1002/Hep.30515 |
0.695 |
|
| 2019 |
Venkateswaran S, Somineni HK, Kilaru V, Hyams JS, Denson LA, Cutler DJ, Smith AK, Conneely KN, Kugathasan S. Tu1159 – Blood Mqtl Effects are Consistent During the Course of the Disease Regardless of Remission Or Relapse Status in Pediatric Crohn’s Disease Patients Gastroenterology. 156: S-967. DOI: 10.1016/S0016-5085(19)39373-4 |
0.33 |
|
| 2019 |
Somineni HK, Haritunians T, Simpson CL, Cutler DJ, Okou D, Itan Y, Venkateswaran S, Stevens C, Datta LW, Dhere TA, Lazarev M, Consortium EAAI, Zwick ME, Cho JH, Daly MJ, et al. Su1028 – Whole-Genome Sequencing of African Americans Identifies Novel Rare Variants Associated with Inflammatory Bowel Disease Gastroenterology. 156: S-488-S-489. DOI: 10.1016/S0016-5085(19)38082-5 |
0.8 |
|
| 2019 |
Satterstrom F, Kosmicki J, Wang J, Collins R, de Rubeis S, Breen M, Gerges S, Børglum A, Buxbaum J, Cutler D, Devlin B, Roeder K, Sanders S, Talkowski M, Daly M. 31DISCOVERY AND CHARACTERIZATION OF 102 GENES ASSOCIATED WITH AUTISM FROM EXOME SEQUENCING OF 37,269 INDIVIDUALS European Neuropsychopharmacology. 29: S1083-S1084. DOI: 10.1016/J.Euroneuro.2018.08.038 |
0.342 |
|
| 2018 |
Denson LA, Jurickova I, Karns R, Shaw KA, Cutler DJ, Okou D, Alexander Valencia C, Dodd A, Mondal K, Aronow BJ, Haberman Y, Linn A, Price A, Bezold R, Lake K, et al. Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte-Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's Disease. Inflammatory Bowel Diseases. PMID 30124884 DOI: 10.1093/Ibd/Izy265 |
0.78 |
|
| 2018 |
Shaw KA, Cutler DJ, Okou D, Dodd A, Aronow BJ, Haberman Y, Stevens C, Walters TD, Griffiths A, Baldassano RN, Noe JD, Hyams JS, Crandall WV, Kirschner BS, Heyman MB, et al. Genetic variants and pathways implicated in a pediatric inflammatory bowel disease cohort. Genes and Immunity. PMID 29593342 DOI: 10.1038/S41435-018-0015-2 |
0.814 |
|
| 2018 |
Venkateswaran S, Prince J, Cutler DJ, Marigorta UM, Okou DT, Prahalad S, Mack D, Boyle B, Walters T, Griffiths A, Sauer CG, LeLeiko N, Keljo D, Markowitz J, Baker SS, et al. Enhanced Contribution of HLA in Pediatric Onset Ulcerative Colitis. Inflammatory Bowel Diseases. 24: 829-838. PMID 29562276 DOI: 10.1093/Ibd/Izx084 |
0.8 |
|
| 2018 |
Denson LA, Jurickova I, Karns R, Shaw KA, Cutler DJ, Okou D, Dodd A, Quinn K, Mondal K, Aronow BJ, Haberman Y, Linn A, Price A, Bezold R, Lake K, et al. Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients with Crohn's Disease. Gastroenterology. PMID 29454792 DOI: 10.1053/J.Gastro.2018.02.016 |
0.783 |
|
| 2018 |
Kotlar AV, Trevino CE, Zwick ME, Cutler DJ, Wingo TS. Bystro: rapid online variant annotation and natural-language filtering at whole-genome scale. Genome Biology. 19: 14. PMID 29409527 DOI: 10.1186/S13059-018-1387-3 |
0.605 |
|
| 2018 |
Somineni HK, Venkateswaran S, Kilaru V, Chopra P, Okou DT, Hyams JS, Denson LA, Cutler DJ, Gibson G, Conneely KN, Smith AK, Kugathasan S. 10 EPIGENOME-WIDE ASSOCIATION STUDY IDENTIFIED SHARED METHYLOMIC CONTRIBUTIONS TO SUSCEPTIBILITY AND PROGRESSION IN PEDIATRIC CROHN’S DISEASE Inflammatory Bowel Diseases. 24: S71-S71. DOI: 10.1093/ibd/izy038.017 |
0.704 |
|
| 2018 |
Somineni HK, Venkateswaran S, Kilaru V, Chopra P, Okou DT, Hyams JS, Denson LA, Cutler DJ, Gibson G, Conneely KN, Smith AK, Kugathasan S. 10 EPIGENOME-WIDE ASSOCIATION STUDY IDENTIFIED SHARED METHYLOMIC CONTRIBUTIONS TO SUSCEPTIBILITY AND PROGRESSION IN PEDIATRIC CROHN'S DISEASE Gastroenterology. 154: S101. DOI: 10.1053/J.Gastro.2017.11.238 |
0.723 |
|
| 2018 |
Denson LA, Jurickova I, Karns R, Shaw KA, Cutler DJ, Okou D, Dodd A, Mondal K, Aronow BJ, Haberman Y, Linn A, Price A, Bezold R, Lake K, Jackson K, et al. 27 CLINICAL AND GENOMIC CORRELATES OF NEUTROPHIL GRANULOCYTE-MACROPHAGE COLONY STIMULATING FACTOR SIGNALING IN PEDIATRIC CROHN DISEASE Inflammatory Bowel Diseases. 24: S7-S8. DOI: 10.1053/J.Gastro.2017.11.051 |
0.772 |
|
| 2018 |
Jurickova I, Karns R, Cutler DJ, Okou D, Dodd A, Mondal K, Aronow BJ, Haberman Y, Linn A, Price A, Bezold R, Lake K, Jackson K, Walters TD, Griffiths AM, et al. 378 - Genomic Correlates of Reduced Neutrophil Granulocytemacrophage Colony Stimulating Factor Signaling in Stricturing Pediatric Crohn Disease Gastroenterology. 154: S-89-S-90. DOI: 10.1016/S0016-5085(18)30746-7 |
0.777 |
|
| 2017 |
Rambo-Martin BL, Mulle JG, Cutler DJ, Bean LJH, Rosser TC, Dooley KJ, Cua C, Capone G, Maslen CL, Reeves RH, Sherman SL, Zwick ME. Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects. G3 (Bethesda, Md.). PMID 29141989 DOI: 10.1534/G3.117.300366 |
0.639 |
|
| 2017 |
Guo T, Repetto GM, McDonald McGinn DM, Chung JH, Nomaru H, Campbell CL, Blonska A, Bassett AS, Chow EWC, Mlynarski EE, Swillen A, Vermeesch J, Devriendt K, Gothelf D, Carmel M, ... ... Cutler DJ, et al. Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3. Circulation. Cardiovascular Genetics. 10. PMID 29025761 DOI: 10.1161/Circgenetics.116.001690 |
0.311 |
|
| 2017 |
Johnston HR, Chopra P, Wingo TS, Patel V, Epstein MP, Mulle JG, Warren ST, Zwick ME, Cutler DJ. Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizes. Proceedings of the National Academy of Sciences of the United States of America. PMID 28916730 DOI: 10.1073/Pnas.1714535114 |
0.609 |
|
| 2017 |
Wingo TS, Duong DM, Zhou M, Dammer EB, Wu H, Cutler DJ, Lah JJ, Levey AI, Seyfried NT. Integrating Next-Generation Genomic Sequencing and Mass Spectrometry to Estimate Allele-Specific Protein Abundance in Human Brain. Journal of Proteome Research. PMID 28691493 DOI: 10.1021/Acs.Jproteome.7B00324 |
0.323 |
|
| 2017 |
Johnston HR, Chopra P, Wingo TS, Patel V, Epstein MP, Mulle JG, Warren ST, Zwick ME, Cutler DJ. PEMapper and PECaller provide a simplified approach to whole-genome sequencing. Proceedings of the National Academy of Sciences of the United States of America. PMID 28223510 DOI: 10.1073/Pnas.1618065114 |
0.627 |
|
| 2017 |
Kosmicki JA, Samocha KE, Howrigan DP, Sanders SJ, Slowikowski K, Lek M, Karczewski KJ, Cutler DJ, Devlin B, Roeder K, Buxbaum JD, Neale BM, MacArthur DG, Wall DP, Robinson EB, et al. Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples. Nature Genetics. PMID 28191890 DOI: 10.1038/Ng.3789 |
0.385 |
|
| 2017 |
Wingo TS, Kotlar A, Cutler DJ. MPD: multiplex primer design for next-generation targeted sequencing. Bmc Bioinformatics. 18: 14. PMID 28056760 DOI: 10.1186/S12859-016-1453-3 |
0.349 |
|
| 2017 |
Denson LA, Jurickova I, Shaw K, Linn A, Dodd A, Okou D, Chalk C, Bonkowski E, Griffiths AM, Baldassano RN, Noe JD, Hyams JS, Crandall WV, Heyman MB, Snapper SB, ... ... Cutler DJ, et al. Low Neutrophil Reactive Oxygen Species Production is Associated with Nicotinamide-Adenine Dinucleotide Phosphate (NADPH) Oxidase Gene Mutations and Refractory Colonic Involvement in Pediatric Crohn Disease Gastroenterology. 152: S955. DOI: 10.1016/S0016-5085(17)33247-X |
0.759 |
|
| 2017 |
Denson LA, Jurickova I, Shaw K, Linn A, Dodd A, Okou D, Chalk C, Bonkowski E, Griffiths AM, Baldassano RN, Noe JD, Hyams JS, Crandall WV, Heyman MB, Snapper SB, ... ... Cutler DJ, et al. Reduced Neutrophil Granulocyte-Macrophage Colony Stimulating Factor Signaling is Associated with Granulocyte-Macrophage Colony Stimulating Factor Receptor Alpha Chain Gene Mutations and Stricturing Disease Complications in Pediatric Crohn Disease Gastroenterology. 152: S955. DOI: 10.1016/S0016-5085(17)33246-8 |
0.762 |
|
| 2017 |
Prince J, Venkateswaran S, Cutler DJ, Okou D, Chopra P, Davis S, Baker SS, Strople JA, Hommel KA, Evans JS, Sauer CG, Markowitz J, Rufo PA, Pfefferkorn MD, Ziring D, et al. Greater Contribution of HLA to Risk for Pediatric-Onset Ulcerative Colitis Can be Narrowed to 3 Independent Classic HLA Variants and Corresponding Amino Acid Changes Gastroenterology. 152: S954. DOI: 10.1016/S0016-5085(17)33244-4 |
0.677 |
|
| 2016 |
Brant SR, Okou DT, Simpson CL, Cutler DJ, Haritunians T, Bradfield JP, Chopra P, Prince J, Begum F, Kumar A, Huang C, Venkateswaran S, Datta LW, Wei Z, Thomas K, et al. Genome-wide Association Study Identifies African-Specific Susceptibility Loci in African Americans with Inflammatory Bowel Disease. Gastroenterology. PMID 27693347 DOI: 10.1053/J.Gastro.2016.09.032 |
0.8 |
|
| 2016 |
Broadaway KA, Cutler DJ, Duncan R, Moore JL, Ware EB, Jhun MA, Bielak LF, Zhao W, Smith JA, Peyser PA, Kardia SL, Ghosh D, Epstein MP. A Statistical Approach for Testing Cross-Phenotype Effects of Rare Variants. American Journal of Human Genetics. 98: 525-540. PMID 26942286 DOI: 10.1016/J.Ajhg.2016.01.017 |
0.366 |
|
| 2015 |
Huang C, Haritunians T, Okou DT, Cutler DJ, Zwick ME, Taylor KD, Datta LW, Maranville JC, Liu Z, Ellis S, Chopra P, Alexander JS, Baldassano RN, Cross RK, Dassopoulos T, et al. Characterization of Genetic Loci That Affect Susceptibility to Inflammatory Bowel Diseases in African Americans. Gastroenterology. PMID 26278503 DOI: 10.1053/J.Gastro.2015.07.065 |
0.796 |
|
| 2015 |
Ramachandran D, Zeng Z, Locke AE, Mulle JG, Bean LJ, Rosser TC, Dooley KJ, Cua CL, Capone GT, Reeves RH, Maslen CL, Cutler DJ, Feingold E, Sherman SL, Zwick ME. Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. G3 (Bethesda, Md.). 5: 1961-71. PMID 26194203 DOI: 10.1534/G3.115.019943 |
0.659 |
|
| 2015 |
Cutler DJ, Zwick ME, Okou DT, Prahalad S, Walters T, Guthery SL, Dubinsky M, Baldassano R, Crandall WV, Rosh J, Markowitz J, Stephens M, Kellermayer R, Pfefferkorn M, Heyman MB, et al. Dissecting Allele Architecture of Early Onset IBD Using High-Density Genotyping. Plos One. 10: e0128074. PMID 26098103 DOI: 10.1371/Journal.Pone.0128074 |
0.802 |
|
| 2015 |
Tran TT, Liu Y, Zwick ME, Ramachandran D, Cutler DJ, Huang X, Berry GT, Fridovich-Keil JL. A De Novo Variant in Galactose-1-P Uridylyltransferase (GALT) Leading to Classic Galactosemia. Jimd Reports. 19: 1-6. PMID 25681079 DOI: 10.1007/8904_2014_349 |
0.587 |
|
| 2015 |
Johnston HR, Hu Y, Cutler DJ. Population genetics identifies challenges in analyzing rare variants. Genetic Epidemiology. 39: 145-8. PMID 25640419 DOI: 10.1002/Gepi.21881 |
0.381 |
|
| 2015 |
Ramachandran D, Mulle JG, Locke AE, Bean LJ, Rosser TC, Bose P, Dooley KJ, Cua CL, Capone GT, Reeves RH, Maslen CL, Cutler DJ, Sherman SL, Zwick ME. Contribution of copy-number variation to Down syndrome-associated atrioventricular septal defects. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 554-60. PMID 25341113 DOI: 10.1038/Gim.2014.144 |
0.621 |
|
| 2015 |
Brant SR, Huang C, Haritunians T, Okou DT, Cutler DJ, Zwick ME, Datta LW, Taylor KD, Rotter JI, Bridges S, Kimberly RP, Rich SS, McGovern D, Kugathasan S. 387 Immunochip Implicates Multiple Genetic Loci for African American IBD Including HLA-DRB1*1502 for UC, NOD2, PTGER4, IL23R, LZKF3 and STAT5A/STAT3 for CD and Several Regions of Significant Admixture Linkage Disequilibrium Gastroenterology. 148: S-80. DOI: 10.1016/S0016-5085(15)30281-X |
0.777 |
|
| 2014 |
De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, ... ... Cutler DJ, et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 515: 209-15. PMID 25363760 DOI: 10.1038/Nature13772 |
0.611 |
|
| 2014 |
Okou DT, Mondal K, Faubion WA, Kobrynski LJ, Denson LA, Mulle JG, Ramachandran D, Xiong Y, Svingen P, Patel V, Bose P, Waters JP, Prahalad S, Cutler DJ, Zwick ME, et al. Exome sequencing identifies a novel FOXP3 mutation in a 2-generation family with inflammatory bowel disease. Journal of Pediatric Gastroenterology and Nutrition. 58: 561-8. PMID 24792626 DOI: 10.1097/Mpg.0000000000000302 |
0.794 |
|
| 2014 |
Mulle JG, Pulver AE, McGrath JA, Wolyniec PS, Dodd AF, Cutler DJ, Sebat J, Malhotra D, Nestadt G, Conrad DF, Hurles M, Barnes CP, Ikeda M, Iwata N, Levinson DF, et al. Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia. Biological Psychiatry. 75: 371-7. PMID 23871472 DOI: 10.1016/J.Biopsych.2013.05.040 |
0.333 |
|
| 2014 |
Prahalad S, Marion MC, Cobb J, Sudman M, Hinks A, Pichavant M, Ponder L, Reed AM, Wallace C, Becker ML, Yeung RSM, Rosenberg AM, Punaro MG, Mellins ED, Nelson JL, ... ... Cutler D, et al. A159: The Autoimmune Genetic Architecture of Childhood Onset Rheumatoid Arthritis Arthritis & Rheumatology. 66: S205-S206. DOI: 10.1002/Art.38585 |
0.382 |
|
| 2013 |
Johnston HR, Cutler DJ. A comprehensive search for recombinogenic motifs in the human genome. Plos One. 8: e62920. PMID 23626862 DOI: 10.1371/Journal.Pone.0062920 |
0.307 |
|
| 2013 |
Prahalad S, Conneely KN, Jiang Y, Sudman M, Wallace CA, Brown MR, Ponder LA, Rohani-Pichavant M, Zwick ME, Cutler DJ, Angeles-Han ST, Vogler LB, Kennedy C, Rouster-Stevens K, Wise CA, et al. Susceptibility to childhood-onset rheumatoid arthritis: investigation of a weighted genetic risk score that integrates cumulative effects of variants at five genetic loci. Arthritis and Rheumatism. 65: 1663-7. PMID 23450725 DOI: 10.1002/Art.37913 |
0.615 |
|
| 2013 |
Kugathasan S, Okou DT, Mondal K, Benjamin AL, Kumar A, Hussain SZ, Katz J, Cross R, Moulton DE, Cutler DJ, Zwick ME. Su1743 Exome Sequencing Identify Novel Variants in African-Americans With Severe Perianal and Colonic Crohn's Disease Gastroenterology. 144: S-465. DOI: 10.1016/S0016-5085(13)61720-5 |
0.751 |
|
| 2013 |
Kugathasan S, Dubinsky M, Guthery SL, Okou DT, Bose P, Zwick ME, Cutler DJ, Waters JP, Hyams JS, Baldassano R, Stephens MC, Heyman MB, Griffiths AM, Crandall W, Markowitz J, et al. 976 Early Onset Crohn's Disease Exhibit Distinct Allele Architecture Differences and Reveal New IBD Loci Gastroenterology. 144: S-178. DOI: 10.1016/S0016-5085(13)60634-4 |
0.781 |
|
| 2012 |
Steinberg KM, Ramachandran D, Patel VC, Shetty AC, Cutler DJ, Zwick ME. Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder. Molecular Autism. 3: 8. PMID 23020841 DOI: 10.1186/2040-2392-3-8 |
0.688 |
|
| 2012 |
Mondal K, Ramachandran D, Patel VC, Hagen KR, Bose P, Cutler DJ, Zwick ME. Excess variants in AFF2 detected by massively parallel sequencing of males with autism spectrum disorder. Human Molecular Genetics. 21: 4356-64. PMID 22773736 DOI: 10.1093/Hmg/Dds267 |
0.636 |
|
| 2012 |
Johnston HR, Cutler DJ. Population demographic history can cause the appearance of recombination hotspots. American Journal of Human Genetics. 90: 774-83. PMID 22560089 DOI: 10.1016/J.Ajhg.2012.03.011 |
0.314 |
|
| 2012 |
Adeyanju O, Okou DT, Huang C, Kumar A, Sauer C, Galloway C, Prasad M, Waters J, Cutler DJ, Zwick ME, Dhere T, Kugathasan S. Common NOD2 risk variants in African Americans with Crohn's disease are due exclusively to recent Caucasian admixture. Inflammatory Bowel Diseases. 18: 2357-9. PMID 22447396 DOI: 10.1002/Ibd.22944 |
0.79 |
|
| 2012 |
Sun M, Mondal K, Patel V, Horner VL, Long AB, Cutler DJ, Caspary T, Zwick ME. Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse. G3 (Bethesda, Md.). 2: 143-50. PMID 22384391 DOI: 10.1534/G3.111.001669 |
0.636 |
|
| 2012 |
Judy JT, Seifuddin F, Mahon PB, Huo Y, Goes FS, Jancic D, Schweizer B, Mondimore FM, Mackinnon DF, Depaulo JR, Gershon ES, McMahon FJ, Cutler DJ, Zandi PP, Potash JB, et al. Association study of serotonin pathway genes in attempted suicide. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 112-9. PMID 22170779 DOI: 10.1002/Ajmg.B.32008 |
0.348 |
|
| 2012 |
Wingo TS, Lah JJ, Levey AI, Cutler DJ. Autosomal recessive causes likely in early-onset Alzheimer disease. Archives of Neurology. 69: 59-64. PMID 21911656 DOI: 10.1001/Archneurol.2011.221 |
0.315 |
|
| 2012 |
Prahalad S, Brown M, Thompson SD, Zwick M, Cutler D, Ponder LA, Prozonic J, Angeles-Han S, Vogler LB, Kennedy CW, Wallace CA, Wise C, Punaro MG, Reed AM, Park JL, et al. Susceptibility to childhood onset rheumatoid arthritis: investigation of a weighted genetic risk score that integrates cumulative effects of five genetic risk variants Pediatric Rheumatology. 10. DOI: 10.1186/1546-0096-10-S1-A116 |
0.625 |
|
| 2011 |
Wingo TS, Cutler DJ, Yarab N, Kelly CM, Glass JD. The heritability of amyotrophic lateral sclerosis in a clinically ascertained United States research registry. Plos One. 6: e27985. PMID 22132186 DOI: 10.1371/Journal.Pone.0027985 |
0.309 |
|
| 2011 |
Wright FA, Strug LJ, Doshi VK, Commander CW, Blackman SM, Sun L, Berthiaume Y, Cutler D, Cojocaru A, Collaco JM, Corey M, Dorfman R, Goddard K, Green D, Kent JW, et al. Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. Nature Genetics. 43: 539-46. PMID 21602797 DOI: 10.1038/Ng.838 |
0.376 |
|
| 2011 |
Mondal K, Shetty AC, Patel V, Cutler DJ, Zwick ME. Targeted sequencing of the human X chromosome exome. Genomics. 98: 260-5. PMID 21524701 DOI: 10.1016/J.Ygeno.2011.04.004 |
0.616 |
|
| 2011 |
Wang W, Shen P, Thiyagarajan S, Lin S, Palm C, Horvath R, Klopstock T, Cutler D, Pique L, Schrijver I, Davis RW, Mindrinos M, Speed TP, Scharfe C. Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing. Nucleic Acids Research. 39: 44-58. PMID 20843780 DOI: 10.1093/Nar/Gkq750 |
0.359 |
|
| 2011 |
Adeyanju O, Okou D, Huang C, Sauer C, Prasad M, Waters J, Ifeadike W, Benjamin A, Labaze S, Cutler D, Zwick M, Dhere T, Kugathasan S. Risk of NOD2 in African-American subjects with Crohnʼs disease is exclusively contributed by Caucasian admixture Inflammatory Bowel Diseases. 17: S77-S78. DOI: 10.1097/00054725-201112002-00255 |
0.758 |
|
| 2011 |
Wingo T, Levey A, Lah J, Cutler D. Early-onset Alzheimer's disease likely has autosomal recessive causes Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.09.088 |
0.333 |
|
| 2010 |
Patel VC, Mondal K, Shetty AC, Horner VL, Bedoyan JK, Martin D, Caspary T, Cutler DJ, Zwick ME. Microarray oligonucleotide probe designer (MOPeD): A web service. Open Access Bioinformatics. 2: 145-155. PMID 21379402 DOI: 10.2147/OAB.S13741 |
0.615 |
|
| 2010 |
Cutler DJ, Jensen JD. To pool, or not to pool? Genetics. 186: 41-3. PMID 20855575 DOI: 10.1534/Genetics.110.121012 |
0.374 |
|
| 2010 |
Shetty AC, Athri P, Mondal K, Horner VL, Steinberg KM, Patel V, Caspary T, Cutler DJ, Zwick ME. SeqAnt: a web service to rapidly identify and annotate DNA sequence variations. Bmc Bioinformatics. 11: 471. PMID 20854673 DOI: 10.1186/1471-2105-11-471 |
0.642 |
|
| 2010 |
Collins SC, Bray SM, Suhl JA, Cutler DJ, Coffee B, Zwick ME, Warren ST. Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males. American Journal of Medical Genetics. Part A. 152: 2512-20. PMID 20799337 DOI: 10.1002/Ajmg.A.33626 |
0.645 |
|
| 2010 |
Mulle JG, Dodd AF, McGrath JA, Wolyniec PS, Mitchell AA, Shetty AC, Sobreira NL, Valle D, Rudd MK, Satten G, Cutler DJ, Pulver AE, Warren ST. Microdeletions of 3q29 confer high risk for schizophrenia. American Journal of Human Genetics. 87: 229-36. PMID 20691406 DOI: 10.1016/J.Ajhg.2010.07.013 |
0.38 |
|
| 2010 |
Mulle JG, Patel VC, Warren ST, Hegde MR, Cutler DJ, Zwick ME. Empirical evaluation of oligonucleotide probe selection for DNA microarrays. Plos One. 5: e9921. PMID 20360966 DOI: 10.1371/Journal.Pone.0009921 |
0.591 |
|
| 2010 |
Collins SC, Coffee B, Benke PJ, Berry-Kravis E, Gilbert F, Oostra B, Halley D, Zwick ME, Cutler DJ, Warren ST. Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype. Plos One. 5: e9476. PMID 20221430 DOI: 10.1371/Journal.Pone.0009476 |
0.615 |
|
| 2010 |
Cutler DJ, Abecasis GR. Response to Graffelman: Tests of Hardy-Weinberg Equilibrium American Journal of Human Genetics. 86: 818-819. DOI: 10.1016/J.Ajhg.2010.03.012 |
0.326 |
|
| 2009 |
McDougal KE, Fallin MD, Moller DR, Song Z, Cutler DJ, Steiner LL, Cutting GR. Variation in the lymphotoxin-alpha/tumor necrosis factor locus modifies risk of erythema nodosum in sarcoidosis. The Journal of Investigative Dermatology. 129: 1921-6. PMID 19225544 DOI: 10.1038/Jid.2008.456 |
0.378 |
|
| 2009 |
Carney AE, Sanders RD, Garza KR, McGaha LA, Bean LJ, Coffee BW, Thomas JW, Cutler DJ, Kurtkaya NL, Fridovich-Keil JL. Origins, distribution and expression of the Duarte-2 (D2) allele of galactose-1-phosphate uridylyltransferase. Human Molecular Genetics. 18: 1624-32. PMID 19224951 DOI: 10.1093/Hmg/Ddp080 |
0.327 |
|
| 2009 |
Willour VL, Chen H, Toolan J, Belmonte P, Cutler DJ, Goes FS, Zandi PP, Lee RS, MacKinnon DF, Mondimore FM, Schweizer B, DePaulo JR, Gershon ES, et al. Family-based association of FKBP5 in bipolar disorder. Molecular Psychiatry. 14: 261-8. PMID 18180755 DOI: 10.1038/Sj.Mp.4002141 |
0.361 |
|
| 2008 |
Bremer LA, Blackman SM, Vanscoy LL, McDougal KE, Bowers A, Naughton KM, Cutler DJ, Cutting GR. Interaction between a novel TGFB1 haplotype and CFTR genotype is associated with improved lung function in cystic fibrosis. Human Molecular Genetics. 17: 2228-37. PMID 18424453 DOI: 10.1093/Hmg/Ddn123 |
0.326 |
|
| 2008 |
Lin S, Carvalho B, Cutler DJ, Arking DE, Chakravarti A, Irizarry RA. Validation and extension of an empirical Bayes method for SNP calling on Affymetrix microarrays. Genome Biology. 9: R63. PMID 18387188 DOI: 10.1186/Gb-2008-9-4-R63 |
0.455 |
|
| 2008 |
Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, Rea A, Guy M, Lin S, Cook EH, Chakravarti A. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. American Journal of Human Genetics. 82: 160-4. PMID 18179894 DOI: 10.1016/J.Ajhg.2007.09.015 |
0.56 |
|
| 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, ... ... Cutler DJ, et al. Genome-wide detection and characterization of positive selection in human populations. Nature. 449: 913-8. PMID 17943131 DOI: 10.1038/Nature06250 |
0.529 |
|
| 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, ... ... Cutler DJ, et al. A second generation human haplotype map of over 3.1 million SNPs. Nature. 449: 851-61. PMID 17943122 DOI: 10.1038/Nature06258 |
0.53 |
|
| 2007 |
Okou DT, Steinberg KM, Middle C, Cutler DJ, Albert TJ, Zwick ME. Microarray-based genomic selection for high-throughput resequencing. Nature Methods. 4: 907-9. PMID 17934469 DOI: 10.1038/Nmeth1109 |
0.764 |
|
| 2007 |
Kohler JR, Cutler DJ. Simultaneous discovery and testing of deletions for disease association in SNP genotyping studies. American Journal of Human Genetics. 81: 684-99. PMID 17846995 DOI: 10.1086/520823 |
0.383 |
|
| 2007 |
Gherman A, Chen PE, Teslovich TM, Stankiewicz P, Withers M, Kashuk CS, Chakravarti A, Lupski JR, Cutler DJ, Katsanis N. Population bottlenecks as a potential major shaping force of human genome architecture. Plos Genetics. 3: e119. PMID 17658953 DOI: 10.1371/Journal.Pgen.0030119 |
0.516 |
|
| 2007 |
Verma R, Cutler DJ, Holmans P, Knowles JA, Crowe RR, Scheftner WA, Weissman MM, DePaulo JR, Levinson DF, Potash JB. Investigating the role of p11 (S100A10) sequence variation in susceptibility to major depression. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 1079-82. PMID 17510952 DOI: 10.1002/Ajmg.B.30514 |
0.338 |
|
| 2006 |
Blackman SM, Deering-Brose R, McWilliams R, Naughton K, Coleman B, Lai T, Algire M, Beck S, Hoover-Fong J, Hamosh A, Fallin MD, West K, Arking DE, Chakravarti A, Cutler DJ, et al. Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis. Gastroenterology. 131: 1030-9. PMID 17030173 DOI: 10.1053/J.Gastro.2006.07.016 |
0.471 |
|
| 2006 |
Zhou S, Kassauei K, Cutler DJ, Kennedy GC, Sidransky D, Maitra A, Califano J. An oligonucleotide microarray for high-throughput sequencing of the mitochondrial genome. The Journal of Molecular Diagnostics : Jmd. 8: 476-82. PMID 16931588 DOI: 10.2353/Jmoldx.2006.060008 |
0.332 |
|
| 2005 |
Maitra A, Arking DE, Shivapurkar N, Ikeda M, Stastny V, Kassauei K, Sui G, Cutler DJ, Liu Y, Brimble SN, Noaksson K, Hyllner J, Schulz TC, Zeng X, Freed WJ, et al. Genomic alterations in cultured human embryonic stem cells. Nature Genetics. 37: 1099-103. PMID 16142235 DOI: 10.1038/Ng1631 |
0.499 |
|
| 2005 |
Mitchell AA, Chakravarti A, Cutler DJ. On the probability that a novel variant is a disease-causing mutation. Genome Research. 15: 960-6. PMID 15965029 DOI: 10.1101/Gr.3761405 |
0.541 |
|
| 2005 |
Emison ES, McCallion AS, Kashuk CS, Bush RT, Grice E, Lin S, Portnoy ME, Cutler DJ, Green ED, Chakravarti A. A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk. Nature. 434: 857-63. PMID 15829955 DOI: 10.1038/Nature03467 |
0.585 |
|
| 2005 |
Wigginton JE, Cutler DJ, Abecasis GR. A note on exact tests of Hardy-Weinberg equilibrium. American Journal of Human Genetics. 76: 887-93. PMID 15789306 DOI: 10.1086/429864 |
0.306 |
|
| 2005 |
Zwick ME, Mcafee F, Cutler DJ, Read TD, Ravel J, Bowman GR, Galloway DR, Mateczun A. Microarray-based resequencing of multiple Bacillus anthracis isolates. Genome Biology. 6: R10. PMID 15642093 DOI: 10.1186/Gb-2004-6-1-R10 |
0.631 |
|
| 2004 |
Lin S, Chakravarti A, Cutler DJ. Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies. Nature Genetics. 36: 1181-8. PMID 15502828 DOI: 10.1038/Ng1457 |
0.582 |
|
| 2004 |
Lin S, Chakravarti A, Cutler DJ. Haplotype and missing data inference in nuclear families. Genome Research. 14: 1624-32. PMID 15256514 DOI: 10.1101/Gr.2204604 |
0.496 |
|
| 2004 |
Wong CW, Albert TJ, Vega VB, Norton JE, Cutler DJ, Richmond TA, Stanton LW, Liu ET, Miller LD. Tracking the evolution of the SARS coronavirus using high-throughput, high-density resequencing arrays. Genome Research. 14: 398-405. PMID 14993206 DOI: 10.1101/Gr.2141004 |
0.363 |
|
| 2004 |
Mitchell AA, Zwick ME, Chakravarti A, Cutler DJ. Discrepancies in dbSNP confirmation rates and allele frequency distributions from varying genotyping error rates and patterns. Bioinformatics (Oxford, England). 20: 1022-32. PMID 14764571 DOI: 10.1093/Bioinformatics/Bth034 |
0.66 |
|
| 2003 |
Thomas JW, Touchman JW, Blakesley RW, Bouffard GG, Beckstrom-Sternberg SM, Margulies EH, Blanchette M, Siepel AC, Thomas PJ, McDowell JC, Maskeri B, Hansen NF, Schwartz MS, Weber RJ, Kent WJ, ... ... Cutler DJ, et al. Comparative analyses of multi-species sequences from targeted genomic regions. Nature. 424: 788-93. PMID 12917688 DOI: 10.1038/Nature01858 |
0.531 |
|
| 2003 |
Badano JL, Kim JC, Hoskins BE, Lewis RA, Ansley SJ, Cutler DJ, Castellan C, Beales PL, Leroux MR, Katsanis N. Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet-Biedl patients with two mutations at a second BBS locus. Human Molecular Genetics. 12: 1651-9. PMID 12837689 DOI: 10.1093/Hmg/Ddg188 |
0.363 |
|
| 2003 |
Mitchell AA, Cutler DJ, Chakravarti A. Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test. American Journal of Human Genetics. 72: 598-610. PMID 12587097 DOI: 10.1086/368203 |
0.545 |
|
| 2003 |
Marth G, Schuler G, Yeh R, Davenport R, Agarwala R, Church D, Wheelan S, Baker J, Ward M, Kholodov M, Phan L, Czabarka E, Murvai J, Cutler D, Wooding S, et al. Sequence variations in the public human genome data reflect a bottlenecked population history. Proceedings of the National Academy of Sciences of the United States of America. 100: 376-81. PMID 12502794 DOI: 10.1073/Pnas.222673099 |
0.555 |
|
| 2003 |
Belmont JW, Hardenbol P, Willis TD, Yu F, Yang H, Ch'Ang LY, Huang W, Liu B, Shen Y, Tam PKH, Tsui LC, Waye MMY, Wong JTF, Zeng C, Zhang Q, ... ... Cutler DJ, et al. The international HapMap project Nature. 426: 789-796. DOI: 10.1038/Nature02168 |
0.388 |
|
| 2002 |
Lin S, Cutler DJ, Zwick ME, Chakravarti A. Haplotype inference in random population samples. American Journal of Human Genetics. 71: 1129-37. PMID 12386835 DOI: 10.1086/344347 |
0.651 |
|
| 2001 |
Cutler DJ, Zwick ME, Carrasquillo MM, Yohn CT, Tobin KP, Kashuk C, Mathews DJ, Shah NA, Eichler EE, Warrington JA, Chakravarti A. High-throughput variation detection and genotyping using microarrays. Genome Research. 11: 1913-25. PMID 11691856 DOI: 10.1101/Gr.197201 |
0.793 |
|
| 2000 |
Zwick ME, Cutler DJ, Chakravarti A. Patterns of genetic variation in Mendelian and complex traits. Annual Review of Genomics and Human Genetics. 1: 387-407. PMID 11701635 DOI: 10.1146/Annurev.Genom.1.1.387 |
0.655 |
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