Michael E. Zwick, Ph.D. - Publications

Human Genetics Emory University School of Medicine, Atlanta, GA, United States 
Human Genetics

64 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Murphy MM, Johnston HR, Zwick ME. Staff Scientist Perspectives on Onboarding and Professional Development: A Case Study. Journal of Biomolecular Techniques : Jbt. PMID 34121934 DOI: 10.7171/jbt.21-3204-001  0.32
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  0.92
2021 Trevino CE, Rounds JC, Charen K, Shubeck L, Hipp HS, Spencer JB, Johnston HR, Cutler DJ, Zwick ME, Epstein MP, Murray A, Macpherson JN, Mila M, Rodriguez-Revenga L, Berry-Kravis E, et al. Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation. Fertility and Sterility. PMID 34016428 DOI: 10.1016/j.fertnstert.2021.04.021  0.92
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  0.92
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, ... ... Zwick ME, 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  0.92
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, ... ... Zwick ME, 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  0.92
2020 Pollak RM, Zinsmeister MC, Murphy MM, Zwick ME, Mulle JG. New phenotypes associated with 3q29 duplication syndrome: Results from the 3q29 registry. American Journal of Medical Genetics. Part A. PMID 32154651 DOI: 10.1002/Ajmg.A.61540  0.32
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, ... ... Zwick ME, 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  0.92
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, ... ... Zwick ME, 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  0.92
2019 Pollak RM, Murphy MM, Epstein MP, Zwick ME, Klaiman C, Saulnier CA, Mulle JG. Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry. Molecular Autism. 10: 30. PMID 31346402 DOI: 10.1186/S13229-019-0281-5  0.32
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  0.92
2019 Pollak R, Purcell R, Rutkowski T, Malone T, Pachura K, Bassell GJ, Epstein MP, Caspary T, Dawson PA, Jones DP, Warren ST, Weinshenker D, Zwick ME, Mulle JG. T11Metabolic Dysfunction As A Contributor To Phenotypes Of The Schizophrenia-Associated 3Q29 Deletion European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2019.08.210  0.32
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, ... ... Zwick ME, 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  0.92
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, ... ... Zwick ME, 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  0.92
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, ... ... Zwick ME, et al. Enhanced Contribution of HLA in Pediatric Onset Ulcerative Colitis. Inflammatory Bowel Diseases. 24: 829-838. PMID 29562276 DOI: 10.1093/Ibd/Izx084  0.92
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, ... ... Zwick ME, 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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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, ... ... Zwick ME, 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  0.92
2016 Shaw KA, Bertha M, Hofmekler T, Chopra P, Vatanen T, Srivatsa A, Prince J, Kumar A, Sauer C, Zwick ME, Satten GA, Kostic AD, Mulle JG, Xavier RJ, Kugathasan S. Dysbiosis, inflammation, and response to treatment: a longitudinal study of pediatric subjects with newly diagnosed inflammatory bowel disease. Genome Medicine. 8: 75. PMID 27412252 DOI: 10.1186/S13073-016-0331-Y  0.92
2016 Glassford MR, Rosenfeld JA, Freedman AA, Zwick ME, Mulle JG. Novel features of 3q29 deletion syndrome: Results from the 3q29 registry. American Journal of Medical Genetics. Part A. PMID 26738761 DOI: 10.1002/Ajmg.A.37537  0.92
2015 Kotlar AV, Mercer KB, Zwick ME, Mulle JG. New discoveries in schizophrenia genetics reveal neurobiological pathways: A review of recent findings. European Journal of Medical Genetics. PMID 26493318 DOI: 10.1016/J.Ejmg.2015.10.008  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
2014 Qiao Y, Mondal K, Trapani V, Wen J, Carpenter G, Wildin R, Price EM, Gibbons RJ, Eichmeyer J, Jiang R, DuPont B, Martell S, Lewis SM, Robinson WP, O'Driscoll M, ... ... Zwick ME, et al. Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genes. Human Mutation. 35: 58-62. PMID 24130152 DOI: 10.1002/Humu.22465  0.92
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  0.92
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  0.92
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  0.92
2012 Zwick ME, Joseph SJ, Didelot X, Chen PE, Bishop-Lilly KA, Stewart AC, Willner K, Nolan N, Lentz S, Thomason MK, Sozhamannan S, Mateczun AJ, Du L, Read TD. Genomic characterization of the Bacillus cereus sensu lato species: backdrop to the evolution of Bacillus anthracis. Genome Research. 22: 1512-24. PMID 22645259 DOI: 10.1101/Gr.134437.111  0.92
2012 Bedoyan JK, Schaibley VM, Peng W, Bai Y, Mondal K, Shetty AC, Durham M, Micucci JA, Dhiraaj A, Skidmore JM, Kaplan JB, Skinner C, Schwartz CE, Antonellis A, Zwick ME, et al. Disruption of RAB40AL function leads to Martin--Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder. Journal of Medical Genetics. 49: 332-40. PMID 22581972 DOI: 10.1136/Jmedgenet-2011-100575  0.92
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  0.92
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  0.92
2011 Zwick ME, Thomason MK, Chen PE, Johnson HR, Sozhamannan S, Mateczun A, Read TD. Genetic variation and linkage disequilibrium in Bacillus anthracis. Scientific Reports. 1: 169. PMID 22355684 DOI: 10.1038/Srep00169  0.92
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  0.92
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  0.92
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  0.92
2010 Chen PE, Willner KM, Butani A, Dorsey S, George M, Stewart A, Lentz SM, Cook CE, Akmal A, Price LB, Keim PS, Mateczun A, Brahmbhatt TN, Bishop-Lilly KA, Zwick ME, et al. Rapid identification of genetic modifications in Bacillus anthracis using whole genome draft sequences generated by 454 pyrosequencing. Plos One. 5: e12397. PMID 20811637 DOI: 10.1371/Journal.Pone.0012397  0.92
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  0.92
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  0.92
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  0.92
2010 Tang J, Le S, Sun L, Yan X, Zhang M, Macleod J, Leroy B, Northrup N, Ellis A, Yeatman TJ, Liang Y, Zwick ME, Zhao S. Copy number abnormalities in sporadic canine colorectal cancers. Genome Research. 20: 341-50. PMID 20086242 DOI: 10.1101/Gr.092726.109  0.92
2010 Chen PE, Cook C, Stewart AC, Nagarajan N, Sommer DD, Pop M, Thomason B, Thomason MP, Lentz S, Nolan N, Sozhamannan S, Sulakvelidze A, Mateczun A, Du L, Zwick ME, et al. Genomic characterization of the Yersinia genus. Genome Biology. 11: R1. PMID 20047673 DOI: 10.1186/Gb-2010-11-1-R1  0.92
2009 Okou DT, Locke AE, Steinberg KM, Hagen K, Athri P, Shetty AC, Patel V, Zwick ME. Combining microarray-based genomic selection (MGS) with the Illumina Genome Analyzer platform to sequence diploid target regions. Annals of Human Genetics. 73: 502-13. PMID 19573206 DOI: 10.1111/J.1469-1809.2009.00530.X  0.92
2009 Passalacqua KD, Varadarajan A, Ondov BD, Okou DT, Zwick ME, Bergman NH. Structure and complexity of a bacterial transcriptome. Journal of Bacteriology. 191: 3203-11. PMID 19304856 DOI: 10.1128/Jb.00122-09  0.92
2008 Hegde MR, Chin EL, Mulle JG, Okou DT, Warren ST, Zwick ME. Microarray-based mutation detection in the dystrophin gene. Human Mutation. 29: 1091-9. PMID 18663755 DOI: 10.1002/Humu.20831  0.92
2008 Zwick ME, Kiley MP, Stewart AC, Mateczun A, Read TD. Genotyping of Bacillus cereus strains by microarray-based resequencing. Plos One. 3: e2513. PMID 18596941 DOI: 10.1371/Journal.Pone.0002513  0.92
2008 Steinberg KM, Okou DT, Zwick ME. Applying rapid genome sequencing technologies to characterize pathogen genomes. Analytical Chemistry. 80: 520-8. PMID 18320606 DOI: 10.1021/Ac086027Z  0.92
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  0.92
2005 Zwick ME. A genome sequencing center in every lab. European Journal of Human Genetics : Ejhg. 13: 1167-8. PMID 16251888 DOI: 10.1038/Sj.Ejhg.5201504  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
1999 Zwick ME, Cutler DJ, Langley CH. Classic Weinstein: tetrad analysis, genetic variation and achiasmate segregation in Drosophila and humans. Genetics. 152: 1615-29. PMID 10430587  0.92
1999 Zwick ME, Salstrom JL, Langley CH. Genetic variation in rates of nondisjunction: association of two naturally occurring polymorphisms in the chromokinesin nod with increased rates of nondisjunction in Drosophila melanogaster. Genetics. 152: 1605-14. PMID 10430586  0.92
1994 Boyce TM, Zwick ME, Aquadro CF. Mitochondrial DNA in the Bark Weevils: Phylogeny and evolution in the Pissodes strobi species group (Coleoptera: Curculionidae) Molecular Biology and Evolution. 11: 183-194. DOI: 10.1093/Oxfordjournals.Molbev.A040113  0.92
1989 Boyce TM, Zwick ME, Aquadro CF. Mitochondrial DNA in the bark weevils: size, structure and heteroplasmy. Genetics. 123: 825-36. PMID 2612897  0.92
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