Zoran Brkanac

Boston University — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

28h-index2.8kcitations48works2.02yr avg
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Research Topics

Genetics and Neurodevelopmental Disorders(15), Genomic variations and chromosomal abnormalities(10), Autism Spectrum Disorder Research(8), Genomics and Rare Diseases(8), Reading and Literacy Development(6)

Publications47 total

Circulating endocannabinoids and cognitive function in older adults
Alzheimer s & Dementia·2025Open Access
Data Descriptor: Human whole exome genotype data for Alzheimer’s Disease
2022Open Access
Evidence for involvement of GNB1L in autism
UNC Libraries·2020Open Access
Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene
Translational Psychiatry·2019· 36 citedOpen Access
Suppression and facilitation of human neural responses
eLife·2018· 74 citedOpen Access
Author response: Suppression and facilitation of human neural responses
2017Open Access
Caspase-8, association with Alzheimer’s Disease and functional analysis of rare variants
PLoS ONE·2017· 47 citedOpen Access
Suppression and facilitation of human neural responses
2017· 4 citedOpen Access
Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder
Autism Research·2017· 44 citedOpen Access
Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism
Molecular Psychiatry·2016· 40 citedOpen Access
Family‐based genome scan for age at onset of late‐onset Alzheimer's disease in whole exome sequencing data
Genes Brain & Behavior·2015· 17 citedOpen Access
PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers
Bioinformatics·2015· 10 citedOpen Access
Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes
Human Genetics·2015· 64 citedOpen Access
P4‐199: App processing genes case‐control screening and functional analysis in Alzheimer's disease
Alzheimer s & Dementia·2015
R47H Variant of<i>TREM2</i>Associated With Alzheimer Disease in a Large Late-Onset Family
JAMA Neurology·2015· 141 cited
O1‐04‐02: EXOME‐SEQUENCING IN LATE‐ONSET FAMILIES IDENTIFIED ADDITIONAL CANDIDATES GENES FOR ALZHEIMER'S DISEASE
Alzheimer s & Dementia·2014
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease
Nature·2013· 472 citedOpen Access
Supplementary Material for: Identification of Rare Variants from Exome Sequence in a Large Pedigree with Autism
Figshare·2013Open Access
Title Page / Table of Contents
Human Heredity·2012Open Access
Front &amp; Back Matter
Human Heredity·2012
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Frequent Co-authors

Wendy H. Raskind(21), Ellen M. Wijsman(18), Mark Matsushita(12), Raphael Bernier(8), Hervé Perdry(8), Eleftheria Zeggini(8), Druck Reinhardt Druck Basel(8), Robin J. Leach(7), N.H. Chapman(7), Katy Ankenman(7), Hilary Coon(7), Ian B. Stanaway(7), Virginia W. Berninger(6), Nicola H. Chapman(6), Alejandro Q. Nato(6), Elizabeth E. Marchani(6), Carlos Cruchaga(5), Deborah A. Nickerson(5), Christina Cheung(5), Santhosh Girirajan(4)