Michael E. Zwick
Michael E. Zwick
Senior Vice President for Research, Rutgers University
Verified email at - Homepage
Cited by
Cited by
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ...
Nature 515 (7526), 209-215, 2014
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
Microarray-based genomic selection for high-throughput resequencing
DT Okou, KM Steinberg, C Middle, DJ Cutler, TJ Albert, ME Zwick
Nature methods 4 (11), 907-909, 2007
High-throughput variation detection and genotyping using microarrays
DJ Cutler, ME Zwick, MM Carrasquillo, CT Yohn, KP Tobin, C Kashuk, ...
Genome research 11 (11), 1913-1925, 2001
Mitochondrial DNA in the bark weevils: size, structure and heteroplasmy.
TM Boyce, ME Zwick, CF Aquadro
Genetics 123 (4), 825-836, 1989
Dysbiosis, inflammation, and response to treatment: a longitudinal study of pediatric subjects with newly diagnosed inflammatory bowel disease
KA Shaw, M Bertha, T Hofmekler, P Chopra, T Vatanen, A Srivatsa, ...
Genome medicine 8, 1-13, 2016
Structure and complexity of a bacterial transcriptome
KD Passalacqua, A Varadarajan, BD Ondov, DT Okou, ME Zwick, ...
Journal of bacteriology 191 (10), 3203-3211, 2009
Haplotype inference in random population samples
S Lin, DJ Cutler, ME Zwick, A Chakravarti
The American Journal of Human Genetics 71 (5), 1129-1137, 2002
Genomic characterization of the Bacillus cereus sensu lato species: backdrop to the evolution of Bacillus anthracis
ME Zwick, SJ Joseph, X Didelot, PE Chen, KA Bishop-Lilly, AC Stewart, ...
Genome research 22 (8), 1512-1524, 2012
Microarray‐based mutation detection in the dystrophin gene
MR Hegde, ELH Chin, JG Mulle, DT Okou, ST Warren, ME Zwick
Human mutation 29 (9), 1091-1099, 2008
Genome-wide association study identifies African-specific susceptibility loci in African Americans with inflammatory bowel disease
SR Brant, DT Okou, CL Simpson, DJ Cutler, T Haritunians, JP Bradfield, ...
Gastroenterology 152 (1), 206-217. e2, 2017
Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males
SC Collins, SM Bray, JA Suhl, DJ Cutler, B Coffee, ME Zwick, ST Warren
American journal of medical genetics Part A 152 (10), 2512-2520, 2010
Genomic characterization of the Yersinia genus
PE Chen, C Cook, AC Stewart, N Nagarajan, DD Sommer, M Pop, ...
Genome biology 11, 1-18, 2010
Patterns of genetic variation in Mendelian and complex traits
ME Zwick, DJ Cutler, A Chakravarti
Annual review of genomics and human genetics 1 (1), 387-407, 2000
The All of Us Research Program: data quality, utility, and diversity
AH Ramirez, L Sulieman, DJ Schlueter, A Halvorson, J Qian, ...
Patterns 3 (8), 2022
Genetic contributors to risk of schizophrenia in the presence of a 22q11. 2 deletion
I Cleynen, W Engchuan, MS Hestand, T Heung, AM Holleman, ...
Molecular psychiatry 26 (8), 4496-4510, 2021
Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay
M He, LE Kratz, JJ Michel, AN Vallejo, L Ferris, RI Kelley, JJ Hoover, ...
The Journal of clinical investigation 121 (3), 976-984, 2011
Genetic variation in rates of nondisjunction: association of two naturally occurring polymorphisms in the chromokinesin nod with increased rates of nondisjunction in Drosophila …
ME Zwick, JL Salstrom, CH Langley
Genetics 152 (4), 1605-1614, 1999
Microarray-based resequencing of multiple Bacillus anthracisisolates
ME Zwick, F Mcafee, DJ Cutler, TD Read, J Ravel, GR Bowman, ...
Genome biology 6, 1-13, 2005
Novel features of 3q29 deletion syndrome: results from the 3q29 registry
MR Glassford, JA Rosenfeld, AA Freedman, ME Zwick, ...
American journal of medical genetics Part A 170 (4), 999-1006, 2016
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