J. Jaworski

E R Martin, M A Pericak-Vance, J. Gilbert, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants

Derek J Van Booven, J. Gilbert, M. Cuccaro, 2015, Molecular Autism.

Copy Number Variants in Extended Autism Spectrum Disorder Families Reveal Candidates Potentially Involved in Autism Risk

Scott M. Williams, J. Gilbert, M. Cuccaro, 2011, PloS one.

Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2009, Autism research : official journal of the International Society for Autism Research.

Variants in several genomic regions associated with asperger disorder

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2010, Autism research : official journal of the International Society for Autism Research.

Lack of association between autism and SLC25A12.

Eden R Martin, John R Gilbert, Jonathan L Haines, 2006, The American journal of psychiatry.

An Analysis Paradigm for Investigating Multi‐locus Effects in Complex Disease: Examination of Three GABAA Receptor Subunit Genes on 15q11‐q13 as Risk Factors for Autistic Disorder.

E R Martin, M A Pericak-Vance, J. Gilbert, 2006, Annals of human genetics.

Ordered‐subset analysis of savant skills in autism for 15q11‐q13

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes

J. Sutcliffe, J. Gilbert, M. Cuccaro, 2004, Neuroscience Letters.

Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14

J. Gilbert, M. Cuccaro, J. Haines, 2007, Molecular Psychiatry.

A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease

Hiep D. Nguyen, J. Bressler, M. Fornage, 2018, Alzheimer's & Dementia.

Exome Sequencing of Extended Families with Alzheimer’s Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function

M. Pericak-Vance, J. Jaworski, J. Haines, 2017, Journal of Alzheimer's disease & Parkinsonism.

Whole genome sequencing of Caribbean Hispanic families with late‐onset Alzheimer's disease

James Jaworski, Mohamad Saad, Eric Boerwinkle, 2018, Annals of clinical and translational neurology.

A de novo 1.5 Mb microdeletion on chromosome 14q23.2‐23.3 in a patient with autism and spherocytosis

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2011, Autism research : official journal of the International Society for Autism Research.

Investigation of potential gene–gene interactions between apoe and reln contributing to autism risk

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2007, Psychiatric genetics.

An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males

J. Gilbert, H. Hakonarson, Kai Wang, 2011, Molecular autism.

Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease

M. Cuccaro, J. Haines, M. Pericak-Vance, 2016, Alzheimer's & Dementia.

Genome-wide linkage analyses of non-Hispanic White families identifies novel loci for familial late-onset Alzheimer ' s disease

Vance, M. Cuccaro, J. Haines, 2016 .

Variants in several genomic regions associated with asperger disorder

M. Cuccaro, M. Pericak-Vance, J. Jaworski, 2010, Autism research : official journal of the International Society for Autism Research.

Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways.

Scott M. Williams, M. Cuccaro, M. Pericak-Vance, 2012, Human molecular genetics.