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Eli Hatchwell

Research Profile

Disorders

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Kenneth D Gadow; Carla J DeVincent; Saniya Kibria; Sarah F Kirsch; Doreen M Olvet; Victoria I Siegal; Eli Hatchwell
Allele-specific associations of 5-HTTLPR/rs25531 with ADHD and autism spectrum disorder.
Aparna Prasad; Jessica Rickaby; Wendy Roberts; Daisuke Sato; Peggy S Eis; Bridget A Fernandez; Eli Hatchwell; Anath C Lionel; Chao Lu; Christian R Marshall; Daniele Merico; Peter Szatmari; Bhooma Thiruvahindrapuram; John Wei; Stephen W Scherer
A discovery resource of rare copy number variations in individuals with autism spectrum disorder.
Doreen M Olvet; Eli Hatchwell; Greg Hajcak
Lack of association between the 5-HTTLPR and the error-related negativity (ERN).

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All Publications

2013: Kenneth D Gadow; Carla J DeVincent; Saniya Kibria; Sarah F Kirsch; Doreen M Olvet; Victoria I Siegal; Eli Hatchwell
Allele-specific associations of 5-HTTLPR/rs25531 with ADHD and autism spectrum disorder.
Progress in neuro-psychopharmacology & biological psychiatry 2013;40():292-7.
2012: Aparna Prasad; Jessica Rickaby; Wendy Roberts; Daisuke Sato; Peggy S Eis; Bridget A Fernandez; Eli Hatchwell; Anath C Lionel; Chao Lu; Christian R Marshall; Daniele Merico; Peter Szatmari; Bhooma Thiruvahindrapuram; John Wei; Stephen W Scherer
A discovery resource of rare copy number variations in individuals with autism spectrum disorder.
G3 (Bethesda, Md.) 2012;2(12):1665-85.
2010: Doreen M Olvet; Eli Hatchwell; Greg Hajcak
Lack of association between the 5-HTTLPR and the error-related negativity (ERN).
Biological psychology 2010;85(3):504-8.
2010: Sibel Kantarci; Kate G Ackerman; Meaghan K Russell; Mauro Longoni; Carrie Sougnez; Kristin M Noonan; Eli Hatchwell; Xiaoyun Zhang; Rafael Pieretti Vanmarcke; Kwame Anyane-Yeboa; Paul Dickman; Jay Wilson; Patricia K Donahoe; Barbara R Pober
Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH.
American journal of medical genetics. Part A 2010;152A(10):2493-504.
2010: Kenneth D Gadow; Carla J DeVincent; Victoria Pisarevskaya; Doreen M Olvet; Wenjie Xu; Nancy R Mendell; Stephen J Finch; Eli Hatchwell
Parent-child DRD4 genotype as a potential biomarker for oppositional, anxiety, and repetitive behaviors in children with autism spectrum disorder.
Progress in neuro-psychopharmacology & biological psychiatry 2010;34(7):1208-14.
2010: Kenneth D Gadow; Carla J DeVincent; Doreen M Olvet; Victoria Pisarevskaya; Eli Hatchwell
Association of DRD4 polymorphism with severity of oppositional defiant disorder, separation anxiety disorder and repetitive behaviors in children with autism spectrum disorder.
The European journal of neuroscience 2010;32(6):1058-65.
2010: Kenneth D Gadow; Jasmin Roohi; Carla J DeVincent; Sarah Kirsch; Eli Hatchwell
Glutamate transporter gene (SLC1A1) single nucleotide polymorphism (rs301430) and repetitive behaviors and anxiety in children with autism spectrum disorder.
Journal of autism and developmental disorders 2010;40(9):1139-45.
2010: Elizabeth A Mulligan; Eli Hatchwell; Sean R McCorkle; John J Dunn
Differential binding of Escherichia coli McrA protein to DNA sequences that contain the dinucleotide m5CpG.
Nucleic acids research 2010;38(6):1997-2005.
2010: Stephen R Williams; Sureni V Mullegama; Jill A Rosenfeld; Aditi I Dagli; Eli Hatchwell; William P Allen; Charles A Williams; Sarah H Elsea
Haploinsufficiency of MBD5 associated with a syndrome involving microcephaly, intellectual disabilities, severe speech impairment, and seizures.
European journal of human genetics : EJHG 2010;18(4):436-41.
2010: Eli Hatchwell
BAK1 gene variation and abdominal aortic aneurysms-variants are likely due to sequencing of a processed gene on chromosome 20.
Human mutation 2010;31(1):108-9; author reply 110-1.
2009: Kenneth D Gadow; Jasmin Roohi; Carla J DeVincent; Sarah Kirsch; Eli Hatchwell
Association of COMT (Val158Met) and BDNF (Val66Met) gene polymorphisms with anxiety, ADHD and tics in children with autism spectrum disorder.
Journal of autism and developmental disorders 2009;39(11):1542-51.
2009: Mayumi Oda; Jacob L Glass; Reid F Thompson; Yongkai Mo; Emmanuel N Olivier; Maria E Figueroa; Rebecca R Selzer; Todd A Richmond; Xinmin Zhang; Luke Dannenberg; Roland D Green; Ari Melnick; Eli Hatchwell; Eric E Bouhassira; Amit Verma; Masako Suzuki; John M Greally
High-resolution genome-wide cytosine methylation profiling with simultaneous copy number analysis and optimization for limited cell numbers.
Nucleic acids research 2009;37(12):3829-39.
2009: Greg Hajcak; C Castille; Doreen M Olvet; J P Dunning; J Roohi; Eli Hatchwell
Genetic variation in brain-derived neurotrophic factor and human fear conditioning.
Genes, brain, and behavior 2009;8(1):80-5.
2008: Kenneth D Gadow; Jasmin Roohi; Carla J DeVincent; Eli Hatchwell
Association of ADHD, tics, and anxiety with dopamine transporter (DAT1) genotype in autism spectrum disorder.
Journal of child psychology and psychiatry, and allied disciplines 2008;49(12):1331-8.
2008: Susan L Christian; Camille W. Brune; Jyotsna Sudi; Ravinesh A Kumar; Shaung Liu; Samer Karamohamed; Judith A Badner; Seiichi Matsui; Jeffrey Conroy; Devin McQuaid; James Gergel; Eli Hatchwell; T Conrad Gilliam; Elliot S Gershon; Norma J Nowak; William B Dobyns; Edwin H Cook
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
Biological psychiatry 2008;63(12):1111-7.
2008: Jasmin Roohi; David H Tegay; John C Pomeroy; Sandra Burkett; Gary Stone; Roscoe Stanyon; Eli Hatchwell
A de novo apparently balanced translocation [46,XY,t(2;9)(p13;p24)] interrupting RAB11FIP5 identifies a potential candidate gene for autism spectrum disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(4):411-7.
2008: Jizu Zhi; Eli Hatchwell
Human MLPA Probe Design (H-MAPD): a probe design tool for both electrophoresis-based and bead-coupled human multiplex ligation-dependent probe amplification assays.
BMC genomics 2008;9():407.
2008: J Roohi; M Cammer; Cristina Montagna; Eli Hatchwell
An improved method for generating BAC DNA suitable for FISH.
Cytogenetic and genome research 2008;121(1):7-9.
2008: Helga V Toriello; Eli Hatchwell
Toriello-Carey syndrome phenotype and chromosome anomalies.
American journal of medical genetics. Part A 2008;146A(1):116.
2007: Wilson A Lee; Nadine Pernodet; Bingquan Li; Chien H Lin; Eli Hatchwell; Miriam H Rafailovich
Multicomponent polymer coating to block photocatalytic activity of TiO2 nanoparticles.
Chemical communications (Cambridge, England) 2007;(45):4815-7.
2007: Eli Hatchwell; John M Greally
The potential role of epigenomic dysregulation in complex human disease.
Trends in genetics : TIG 2007;23(11):588-95.
2007: Santhosh Girirajan; S R Williams; James Y Garbern; N Nowak; Eli Hatchwell; Sarah H Elsea
17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndrome.
Clinical genetics 2007;72(1):47-58.
2007: Santhosh Girirajan; Roberto Mendoza-Londono; Christopher N Vlangos; Lucie Dupuis; Norma J Nowak; David J Bunyan; Eli Hatchwell; Sarah H Elsea
Smith-Magenis syndrome and Moyamoya disease in a patient with del(17)(p11.2p13.1).
American journal of medical genetics. Part A 2007;143A(9):999-1008.
2007: David H Tegay; Andrew lane; Jasmin Roohi; Eli Hatchwell
Contiguous gene deletion involving L1CAM and AVPR2 causes X-linked hydrocephalus with nephrogenic diabetes insipidus.
American journal of medical genetics. Part A 2007;143(6):594-8.
2006: M R Herbert; J P Russo; S Yang; J Roohi; M Blaxill; Stephen Kahler; L Cremer; Eli Hatchwell
Autism and environmental genomics.
Neurotoxicology 2006;27(5):671-84.
2006: Batbayar Khulan; Reid Thompson; Qian Ye; Melissa Fazzari; Masako Suzuki; Edyta Stasiek; Maria E Figueroa; Jacob L Glass; Quan Chen; Cristina Montagna; Eli Hatchwell; Rebecca R Selzer; Richmond Todd; Roland D Green; Ari Melnick; John M Greally
Comparative isoschizomer profiling of cytosine methylation: the HELP assay.
Genome research 2006;16(8):1046-55.