Publications

Complete List of Published Work in MyBibliography:

http://www.ncbi.nlm.nih.gov/sites/myncbi/michael.zwick.2/bibliography/41149876/public/?sort=date&direction=descending

Bibliography:

a. Published and Accepted Research Articles in Refereed Journals:

1. Boyce TM, Zwick ME, Aquadro CF. 1989. Mitochondrial DNA in the bark weevils: size, structure and heteroplasmy. Genetics 123: 825-836.

2. Boyce TM, Zwick ME, Aquadro CF. 1994. Mitochondrial DNA in the bark weevils: phylogeny and evolution in the Pissodes strobi species group (Coleoptera: Curculionidae). Mol Biol Evol 11: 183-194.

3. Zwick ME, Salstrom JL, Langley CH. 1999. 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: 1605-1614. PMC1460721.

4. Zwick ME, Cutler DJ, Langley CH. 1999. Classic Weinstein: tetrad analysis, genetic variation and achiasmate segregation in Drosophila and humans. Genetics 152: 1615-1629. PMC1460678.

5. Cutler DJ, Zwick ME, Carrasquillo MM, Yohn CT, Tobin KP, Kashuk C, Mathews DJ, Shah NA, Eichler EE, Warrington JA, Chakravarti A. 2001. High-throughput variation detection and genotyping using microarrays. Genome Res 11: 1913-1925.

6. Lin S, Cutler DJ, Zwick ME, Chakravarti A. 2002. Haplotype inference in random population samples. Am J Hum Genet 71: 1129-1137. PMC385088.

7. Mitchell AA, Zwick ME, Chakravarti A, Cutler DJ. 2004. Discrepancies in dbSNP confirmation rates and allele frequency distributions from varying genotyping error rates and patterns. Bioinformatics 20: 1022-1032.

8. Zwick ME, Mcafee F, Cutler DJ, Read TD, Ravel J, Bowman GR, Galloway DR, Mateczun A. 2005. Microarray-based resequencing of multiple Bacillus anthracis isolates. Genome Biol 6: R10. PMC549062.

9. Okou DT, Steinberg KM, Middle C, Cutler DJ, Albert TJ, Zwick ME. 2007. Microarray-based genomic selection for high-throughput resequencing. Nat Methods 4: 907-909.

10. Hegde MR, Chin EL, Mulle JG, Okou DT, Warren ST, Zwick ME. 2008. Microarray-based mutation detection in the dystrophin gene. Hum Mutat 29: 1091-1099. PMC2574813.

11. Zwick ME, Kiley MP, Stewart AC, Mateczun A, Read TD. 2008. Genotyping of Bacillus cereus strains by microarray-based resequencing. PLOS ONE 3: e2513. PMC2438477.

12. Okou DT, Locke AE, Steinberg KM, Hagen K, Athri P, Shetty AC, Patel V, Zwick ME. 2009. Combining microarray-based genomic selection (MGS) with the Illumina Genome Analyzer platform to sequence diploid target regions. Ann Hum Genet 73: 502-513. PMC2729809.

13. Passalacqua KD, Varadarajan A, Ondov BD, Okou DT, Zwick ME, Bergman NH. 2009. Structure and complexity of a bacterial transcriptome. J Bacteriol 191: 3203-3211. PMC2687165.

14. 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, Read TD. 2010. Genomic characterization of the Yersinia genus. Genome Biol 11: R1. PMC2847712.

15. 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, Read TD, Sozhamannan S. 2010. Rapid identification of genetic modifications in Bacillus anthracis using whole genome draft sequences generated by 454 pyrosequencing. PLOS ONE 5: PMC2928293.

16. Collins SC, Coffee B, Benke PJ, Berry-Kravis E, Gilbert F, Oostra B, Halley D, Zwick ME, Cutler DJ, Warren ST. 2010. Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype. PLOS ONE 5: e9476. PMC2832695.

17. Collins SC, Bray SM, Suhl JA, Cutler DJ, Coffee B, Zwick ME, Warren ST. 2010. Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males. Am J Med Genet A 152A: 2512-2520. PMC2946449.

18. Mulle JG, Patel VC, Warren ST, Hegde MR, Cutler DJ, Zwick ME. 2010. Empirical evaluation of oligonucleotide probe selection for DNA microarrays. PLoS ONE 5: e9921. PMC2847945.

19. Patel VC, Mondal K, Shetty AC, Horner VL, Bedoyan JK, Martin D, Caspary T, Cutler DJ, Zwick ME. 2010. Microarray oligonucleotide probe designer (MOPeD): A web service. Open Access Bioinformatics 2: 145-155. PMC3048354.

20. Shetty AC, Athri P, Mondal K, Horner VL, Steinberg KM, Patel V, Caspary T, Cutler DJ, Zwick ME. 2010. SeqAnt: a web service to rapidly identify and annotate DNA sequence variations. BMC Bioinformatics 11: 471. PMC2955049.

21. 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. 2010. Copy number abnormalities in sporadic canine colorectal cancers. Genome Res 20: 341-350. PMC2840980.

22. Zwick ME, Thomason MK, Chen PE, Johnson HR, Sozhamannan S, Mateczun A, Read TD. 2011. Genetic variation and linkage disequilibrium in Bacillus anthracis. Sci Rep 1: Article 169. 1-8. PMC3240990.

23. He M, Kratz LE, Michel JJ, Vallejo AN, Ferris L, Kelley RI, Hoover JJ, Jukic D, Gibson KM, Wolfe LA, Ramachandran D, Zwick ME, Vockley J. 2011. Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay. J Clin Invest 121: 976-984. PMC3049385.

24. Mondal K, Shetty AC, Patel V, Cutler DJ, Zwick ME. 2011. Targeted sequencing of the human X chromosome exome. Genomics 98: 260-265. PMC3154473.

25. Sun M, Mondal K, Patel V, Horner VL, Long AB, Cutler DJ, Caspary T, Zwick ME. 2012. Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse. G3: Genes Genomes Genetics 2: 143-150. PMC3276189.

26. Adeyanju O, Okou DT, Huang C, Kumar A, Sauer C, Galloway C, Prasad M, Waters J, Cutler DJ, Zwick ME, Dhere T, Kugathasan S. 2012. The common NOD2 risk variants in African Americans with Crohn’s disease are due exclusively to recent Caucasian admixture. Inflamm Bowel Dis, in press. PMC3392535.

27. Bedoyan JK, Schaibley V, Peng W, Bai Y, Mondal K, Shetty AC, Durham M, Dhiraaj A, Skidmore J, Kaplan JB, Skinner C, Stevenson RE, Schwartz CE, Antonellis A, Zwick ME, Cavalcoli JD, Li JZ, Martin DM. 2012. Disruption of RAB40AL function leads to Martin-Probst Syndrome, a rare X-linked multisystem neurodevelopmental human disorder. J of Med Genet 49: 332-340. PMC3350147.

28. 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. 2012. Genomic characterization of the Bacillus cereus sensu lato species: backdrop to the evolution of Bacillus anthracis. Genome Research, published online May 29, 2012, doi:10.1101/gr.134437.111. PMC22645259.

29. Mondal K, Ramachandran D, Patel VC, Hagen KR, Bose P, Cutler DJ, Zwick ME. 2012. Excess variants in AFF2 detected by massively parallel sequencing of males with autism spectrum disorder. Hum Mol Genet 21: 4356-4364. PMC3441129.

30. Steinberg KM, Ramachandran D, Patel V, Shetty AC, Cutler DJ, Zwick ME. 2012. Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder. Mol Autism 3: 8. PMC3492087.

31. 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, Punaro M, Reed AM, Mellins ED, Bohnsack JF, Glass DN, Thompson SD. 2013. Susceptibility to childhood-onset rheumatoid arthritis: investigation of a weighted genetic risk score that integrates cumulative effects of variants at five genetic Loci. Arthritis Rheum 65: 1663-1667. PMC3683854.

32. 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, Wolf FI, Zwick ME*, Rajcan-Separovic E. 2014. Variant ATRX Syndrome with Dysfunction of ATRX and MAGT1 Genes. Hum Mutat 35: 58-62. PMC in process. *co-senior author

33. 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, Kugathasan S. 2014. Exome Sequencing Identifies a Novel FOXP3 Mutation in a Two-Generation Family with Inflammatory Bowel Disease. Journal of Pediatric Gastroenterology and Nutrition. PMC4277865.

34. De Rubeis S, He X, Goldberg AP, Poultney C, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Fu S, Aleksic B, Biscaldi M, Bolton PF, Brownfeld JM1,2, Cai J, Campbell NJ, Carracedo A, Chahrour MH, Chiocchetti AG, Coon H, Crawford EL, Crooks L, Curran SR, Dawson G, Duketis E, Fernandez BA, Gallagher L, Geller E, Guter SJ, Hill RS, Ionita-Laza I, Kilpinen H, Klauck SM, Kolevzon A, Lee I, Lehtimaki T, Lin C, Ma'ayan A, Marshall CR, Neale B, Owen MJ, Ozaki N, Parellada M, Parr J, Purcell S, Puura K, Rajagopalan D, Rehnström K, Reichenberg A, Sachse M, Sanders SJ, Schafer C, Schulte-Rüther M, Skuse D, Stevens C, Szatmari P, Tammimies K, Valladares O, Voran A, Wang L, Weiss LA, Willsey JA, Yu TW, Yuen RKC, the DDD Study, Homozygosity Mapping Collaborative for Autism, UK10K Consortium, the Autism Sequencing Consortium, Cook EH, Freitag CM, Gill M, Hultman C, Lehner T, Palotie A, Schellenberg GD, Sklar P, State MW, Sutcliffe JS, Walsh CA, Scherer SW, Zwick ME, Barrett J, Cutler DJ, Roeder K, Devlin B, Daly MJ, Buxbaum JD. 2014. Synaptic, transcriptional, and chromatin genes disrupted in autism, Nature. 515: 209-215. PMC4402723.

35. 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. 2014. Contribution of Copy Number Variation to Down Syndrome-associated Atrioventricular Septal Defects. Genetics in Med. 2014 Oct 23. PMC4408203.

36. Tran T-TV, Liu Y, Zwick ME, Ramachandran D, Cutler DJ, Huang X, Berry GT, Fridovich-Keil JL. 2014. A de novo mutation in galactose-1-P uridylyltransferase (GALT) leading to classic galactosemia. JIMD Rep. 19: 1-6. PMC4501235.

37. 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, LeLeiko N, Mack D, Moulton D, Kappelman MD, Kumar A, Prince J, Bose P, Mondal K, Ramachandran D, Bohnsack JF, Griffiths AM, Haberman Y, Essers J, Thompson SD, Aronow B, Keljo DJ, Hyams JS, Denson LA, Kugathasan S. 2015. Dissecting Allele Architecture of Early Onset IBD Using High-Density Genotyping. PLoS ONE 10: e0128074. *co-first author. PMC4476779.

38. Sanders SJ, He X, Willsey AJ, Ercan-Sencicek AG, Samocha KE, Cicek AE, Murtha MT, Bal VH, Bishop SL, Dong S, Goldberg AP, Jinlu C, Keaney JF, Klei L, Mandell JD, Moreno-De-Luca D, Poultney CS, Robinson EB, Smith L, Solli-Nowlan T, Su MY, Teran NA, Walker MF, Werling DM, Beaudet AL, Cantor RM, Fombonne E, Geschwind DH, Grice DE, Lord C, Lowe JK, Mane SM, Martin DM, Morrow EM, Talkowski ME, Sutcliffe JS, Walsh CA, Yu TW, Autism SC, Ledbetter DH, Martin CL, Cook EH, Buxbaum JD, Daly MJ, Devlin B, Roeder K, State MW. 2015. Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci. Neuron 87: 1215-1233. PMC4624267.

39. Ramachandran D, Zeng Z, Locke A, Mulle JG, Bean LJ, Rosser TC, Dooley KJ, Cua CL, Capone GT, Reeves RH, Maslen CL, Cutler DJ, Feingold E, Sherman SL, and Zwick ME. 2015. Genome-wide Association Study of Down Syndrome-associated Atrioventricular Septal Defects. G3 5(10) 1961-71. PMC4592978.

40. 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, Dhere TA, Duerr RH, Hanson JS, Hou JK, Hussain SZ, Isaacs KL, Kachelries KE, Kader H, Kappelman MD, Katz J, Kellermayer R, Kirschner BS, Kuemmerle JF, Kumar A, Kwon JH, Lazarev M, Mannon P, Moulton DE, Osuntokun BO, Patel A, Rioux JD, Rotter JI, Saeed S, Scherl EJ, Silverberg MS, Silverman A, Targan SR, Valentine JF, Wang MH, Simpson CL, Bridges SL, Kimberly RP, Rich SS, Cho JH, Di Rienzo A, Kao LW, McGovern DP, Brant SR, Kugathasan S. 2015. Characterization of Genetic Loci That Affect Susceptibility to Inflammatory Bowel Diseases in African Americans. Gastroenterology 149: 1575-1586. PMC4685036.

41. Glassford MR, Rosenfeld JA, Freedman AA, Zwick ME, Mulle JG, Unique RCDSG. 2016. Novel features of 3q29 deletion syndrome: Results from the 3q29 registry. Am J Med Genet A 170A: 999-1006. PMC4849199.

42. 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. 2016. Dysbiosis, inflammation, and response to treatment: a longitudinal study of pediatric subjects with newly diagnosed inflammatory bowel disease. Genome Med 8: 75. PMC4944441.

43. 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, Herrinton LJ, Klapproth JA, Quiros AJ, Seminerio J, Liu Z, Alexander JS, Baldassano RN, Dudley-Brown S, Cross RK, Dassopoulos T, Denson LA, Dhere TA, Dryden GW, Hanson JS, Hou JK, Hussain SZ, Hyams JS, Isaacs KL, Kader H, Kappelman MD, Katz J, Kellermayer R, Kirschner BS, Kuemmerle JF, Kwon JH, Lazarev M, Li E, Mack D, Mannon P, Moulton DE, Newberry RD, Osuntokun BO, Patel AS, Saeed SA, Targan SR, Valentine JF, Wang MH, Zonca M, Rioux JD, Duerr RH, Silverberg MS, Cho JH, Hakonarson H, Zwick ME, McGovern DP, Kugathasan S. 2017. Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease. Gastroenterology 152: 206-217.e2. PMC5164948.

44. Lim ET, Uddin M, De Rubeis S, Chan Y, Kamumbu AS, Zhang X, D’Gama AM, Kim SN, Hill RS, Goldberg AP, Poultney C, Minshew NJ, Kushima I, Aleksic B, Ozaki N, Parellada M, Arango C, Penzol MJ, Carracedo A, Kolevzon A, Hultman CM, Weiss LA, Fromer M, Chiocchetti AG, Freitag CM, Autism Sequencing Consortium, Church GM, Scherer SW, Buxbaum JD, Walsh CA. 2017. Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder. Nat Neurosci 20: 1217-1224. PMC5672813.

45. Johnston HR, Chopra P, Wingo TS, Patel V, International COBABIDS, Epstein MP, Mulle JG, Warren ST, Zwick ME, Cutler DJ. 2017. PEMapper and PECaller provide a simplified approach to whole-genome sequencing. Proc Natl Acad Sci U S A 114: E1923-E1932. PMC5347547.

46. Johnston HR, Chopra P, Wingo TS, Patel V, Epstein MP, Mulle JG, Warren ST, Zwick ME, Cutler DJ. 2017. Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizes. Proc Natl Acad Sci U S A 114: E8323. PMC5635938.

47. Sun X, Pittard WS, Xu T, Chen L, Zwick ME, Jiang X, Wang F, Qin ZS. 2017. Omicseq: a web-based search engine for exploring omics datasets. Nucleic Acids Res 45: W445-W452. PMC5793835.

48. Kotlar AV, Trevino CE, Zwick ME, Cutler DJ, Wingo TS. 2018. Bystro: rapid online variant annotation and natural-language filtering at whole-genome scale. Genome Biol 19: 14. PMC5801807.

49. 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. 2018. Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects. 2018. G3 (Bethesda) 8: 105-111. PMC5765339.

50. 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, Jackson K, Walters TD, Griffiths A, Baldassano RN, Noe JD, Hyams JS, Crandall WV, Kirschner BS, Heyman MB, Snapper S, Guthery SL, Dubinsky MC, Leleiko NS, Otley AR, Xavier RJ, Stevens C, Daly MJ, Zwick ME, Kugathasan S. 2018. Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients with Crohn’s Disease. Gastroenterology. PMC5985211.

51. 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, Rosh J, Pfefferkorn M, Heyman MB, Patel A, Otley A, Baldassano R, Noe J, Rufo P, Oliva-Hemker M, Davis S, Zwick ME, Gibson G, Denson LA, Hyams J, Kugathasan S. 2018. Enhanced Contribution of HLA in Pediatric Onset Ulcerative Colitis. Inflamm Bowel Dis 24: 829-838. PMC6350448.

52. Shaw KA, Cutler DJ, Okou D, Epstein MP, Dodd A, Mulle JG, Denson LA, Kugathasan S, Zwick ME. 2018. Genetic variants and pathways implicated in a pediatric inflammatory bowel disease cohort. Genes and Immunity. PMC6162182.

53. Guo T, Diacou A, Nomaru H, McDonald-McGinn DM, Hestand M, Demaerel W, Zhang L, Zhao Y, Ujueta F, Shan J, Montagna C, Zheng D, Crowley TB, Kushan-Wells L, Bearden CE, Kates WR, Gothelf D, Schneider M, Eliez S, Breckpot J, Swillen A, Vorstman J, Zackai E, Benavides Gonzalez F, Repetto GM, Emanuel BS, Bassett AS, Vermeesch JR, Marshall CR, Morrow BE, International 22q11.2 Brain and Behavior Consortium. 2018. Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2. Hum Mol Genet 27: 1150-1163. PMC6059186.

54. 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. Sci Rep. 2019; 9(1) 9168. doi:10.1038/s41598-019-45701-2. PMCID: PMC6591305.

55. Pollak RM, Murphy MM, Epstein MP, Zwick ME, Klaiman C, Saulnier CA, Emory P, Mulle JG. Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry. Mol Autism. 2019; 10 30. doi:10.1186/s13229-019-0281-5. PMCID: PMC6636128.

56. All OURPI, Denny JC, Rutter JL, Goldstein DB, Philippakis A, Smoller JW, Jenkins G, Dishman E. The “All of Us” Research Program. N Engl J Med. 2019; 381(7) 668-676. doi:10.1056/NEJMsr1809937. PMCID: In Progress.

b. Manuscripts Submitted:

c. Review Articles:

1. Zwick ME, Cutler DJ, Chakravarti A. 2000. Patterns of genetic variation in Mendelian and complex traits. Annu Rev Genomics Hum Genet 1: 387-407.

2. Steinberg KM, Okou DT, Zwick ME. 2008. Applying rapid genome sequencing technologies to characterize pathogen genomes. Anal Chem 80: 520-528.

3. Ezewudo M, Zwick ME. 2013. Evaluating rare variants in complex disorders using next-generation sequencing. Curr Psychiatry Rep 15: 349.

4. Kotlar AV, Mercer KB, Zwick ME, Mulle JG. 2015. New discoveries in schizophrenia genetics reveal neurobiological pathways: A review of recent findings. Eur J Med Genet 58: 704-714. PMC4679408.

d. Symposium Contributions:

1. Zwick ME. 2001. The central role of variation in human genetics. Jurimetrics 42: 133-139.

e. Book Chapters:

1. Zwick ME, Cutler DJ, Chakravarti A. 2001. Genetic Variation Analysis of Neuropsychiatric Traits. In: Chin HR, Moldin SO, editors. Methods in Genomic Neuroscience. Boca Raton: CRC Press. pp. 297-310.

2. Okou DT, Zwick ME. 2008. The Role of Resequencing Arrays in Revolutionizing DNA Sequencing. In: Kim S, Tank H, Mardis ER, editors. Genome Sequencing Technology and Algorithms. Boston: Artech House. pp. 25-42.

3. Ezuwado M, Bose P, Patel V, Zwick ME. 2012. SeqAnt 2012: Recent Developments in Next Generation Sequencing Annotation In: Perez-Sanchez, H, editor. Bioinformatics. Rijeka: InTech.

f. Other Publications:

1. Zwick ME. 2005. A genome sequencing center in every lab. Eur J Hum Genet 13: 1167-1168.

2. Buxbaum JD, Daly MJ, Devlin B, Lehner T, Roeder K, State MW, Autism Sequencing Consortium. 2012. The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders. Neuron 76: 1052-1056. PMC3863639.

3. Gur RE, Bassett AS, McDonald-McGinn DM, Bearden CE, Chow E, Emanuel BS, Owen M, Swillen A, Van den Bree M, Vermeesch J, Warren S, Lehner T, Morrow B, The International 22q11.2 Deletion Syndrome Brain Behavior Consortium. 2017. A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11. 2 Deletion Syndrome Brain Behavior Consortium. Molecular psychiatry 22: 1664.