Author details

Full Name

Zoran Brkanac

Affiliation

University of Washington

ORCID

Career Start Year

1996

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
30664616	Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene.	Transl Psychiatry	2019
27956748	Association of rare missense variants in the second intracellular loop of Na<sub>V</sub>1.7 sodium channels with familial autism.	Mol Psychiatry	2018
29376822	Suppression and facilitation of human neural responses.	Elife	2018
28985224	Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants.	PLoS One	2017
28419775	Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder.	Autism Res	2017
26204995	Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes.	Hum Genet	2015
26394601	Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data.	Genes Brain Behav	2015
26076170	R47H Variant of TREM2 Associated With Alzheimer Disease in a Large Late-Onset Family: Clinical, Genetic, and Neuropathological Study.	JAMA Neurol	2015
26231429	PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers.	Bioinformatics	2015
24336208	Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease.	Nature	2014
22095694	Evidence for involvement of GNB1L in autism.	Am J Med Genet B Neuropsychiatr Genet	2012
23594493	Identification of rare variants from exome sequence in a large pedigree with autism.	Hum Hered	2012
21484596	Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.	J Neurodev Disord	2011
22102821	Relative burden of large CNVs on a range of neurodevelopmental phenotypes.	PLoS Genet	2011
21209939	The effect of algorithms on copy number variant detection.	PLoS One	2010
19409521	IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23.	Am J Hum Genet	2009
18607713	Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci.	Behav Genet	2008
19727434	Pharmacology and genetics of autism: implications for diagnosis and treatment.	Per Med	2008
17450541	Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia.	Am J Med Genet B Neuropsychiatr Genet	2007
16331673	Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity.	Am J Med Genet B Neuropsychiatr Genet	2006
15753956	A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.	Mol Psychiatry	2005
16126608	Genetic determinants of addiction to opioids and cocaine.	Harv Rev Psychiatry	2005
15389770	Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.	Am J Med Genet B Neuropsychiatr Genet	2004
12644968	Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia.	Am J Hum Genet	2003
12649625	Prazosin in PTSD.	J Am Acad Child Adolesc Psychiatry	2003
11992570	Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.	Am J Med Genet	2002
12164726	A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.	Arch Neurol	2002
10188722	Genetic pattern of prostate cancer progression.	Int J Cancer	1999
9718349	Evidence for a novel osteosarcoma tumor-suppressor gene in the chromosome 18 region genetically linked with Paget disease of bone.	Am J Hum Genet	1998
9585582	Identification of cryptic rearrangements in patients with 18q- deletion syndrome.	Am J Hum Genet	1998
9096757	Preferential loss of the paternal alleles in the 18q- syndrome.	Am J Med Genet	1997
9286448	Growth hormone insufficiency associated with haploinsufficiency at 18q23.	Am J Med Genet	1997
8812511	Assignment of the human nuclear hormone receptor, NUC1 (PPARD), to chromosome 6p21.1-p21.2.	Genomics	1996

1 - 33 of 33

Julie S Cohen

Kennedy Krieger Institute

Career Start Year 2007

Number of shared co-authors 1

Kaya Bilguvar

Acibadem Mehmet Ali Aydinlar University

Career Start Year 2005

Number of shared co-authors 3

Jonathan Sebat

University of California San Diego

Career Start Year 2000

Number of shared co-authors 5

Alistair T Pagnamenta

NIHR Biomedical Research Centre, University of Oxford

Career Start Year 1999

Number of shared co-authors 2

Patrick M A Sleiman

The Center for Applied Genomics, Children's Hospital of Philadelphia

Career Start Year 1999

Number of shared co-authors 12

Bridget A Fernandez

Memorial University of Newfoundland

Career Start Year 1999

Number of shared co-authors 4

Matthew W State

UCSF Weill Institute for Neurosciences, University of California san francisco

Career Start Year 1997

Number of shared co-authors 6

Dalila Pinto

Icahn School of Medicine at Mount Sinai

Career Start Year 1997

Number of shared co-authors 8

Timothy W Yu

Harvard Medical School

Career Start Year 1997

Number of shared co-authors 3

Kym M Boycott

Children's Hospital of Eastern Ontario

Career Start Year 1996

Number of shared co-authors 5

Szabolcs Szelinger

College of American Pathologists

Career Start Year 1996

Number of shared co-authors 2

Vandana Shashi

Duke University School of Medicine

Career Start Year 1994

Number of shared co-authors 5

Stanley F Nelson

university of california los angeles

Career Start Year 1993

Number of shared co-authors 7

Kimberly F Doheny

Center for Inherited Disease Research, Johns Hopkins School of Medicine

Career Start Year 1993

Number of shared co-authors 8

Dimitrios Avramopoulos

Johns Hopkins School of Medicine

Career Start Year 1992

Number of shared co-authors 5

Jeffrey R Gruen

Yale Medical School

Career Start Year 1991

Number of shared co-authors 3

Stephen W Scherer

The Hospital for Sick Children

Career Start Year 1990

Number of shared co-authors 11

Suzanne M Leal

Center for Statistical Genetics, Columbia University Medical Center

Career Start Year 1990

Number of shared co-authors 9

Bertram M??ller-Myhsok

Max Planck Institute of Psychiatry

Career Start Year 1989

Number of shared co-authors 10

Markus M N??then

Institute of Human Genetics, University Hospital Bonn

Career Start Year 1989

Number of shared co-authors 17

Daniel H Geschwind

University of California los angeles

Career Start Year 1989

Number of shared co-authors 18

Peter Heutink

German Center for Neurodegenerative Diseases (DZNE).

Career Start Year 1988

Number of shared co-authors 14

James S Sutcliffe

Vanderbilt Genetics Institute, Vanderbilt University

Career Start Year 1988

Number of shared co-authors 5

Anne S Bassett

Institute of Medical Science, University of Toronto

Career Start Year 1986

Number of shared co-authors 6

Joseph D Buxbaum

Icahn School of Medicine at Mount Sinai

Career Start Year 1986

Number of shared co-authors 17

Frances Lucy Raymond

University of Cambridge, UK Cambridge University Hospitals NHS Foundation Trust

Career Start Year 1983

Number of shared co-authors 1

Linda M Brzustowicz

The State University of New Jersey

Career Start Year 1983

Number of shared co-authors 1

Thomas Meitinger

Technical University of Munich, Institute of Human Genetics

Career Start Year 1982

Number of shared co-authors 6

Guy A Rouleau

McGill University, Canada Montreal Neurological Institute and Hospital

Career Start Year 1981

Number of shared co-authors 16

Gholson J Lyon

NYS Institute for Basic Research in Developmental Disabilities .

Career Start Year 1972

Number of shared co-authors 8

row(s) 1 - 30 of 30

Wendy H Raskind

University of Washington School of Medicine

Co-authored papers 19

Mark Matsushita

University of Washington

Co-authored papers 12

Robin J Leach

University of Texas Health San Antonio

Co-authored papers 6

Virginia W Berninger

University of Washington

Co-authored papers 6

Thomas D Bird

University of Washington School of Medicine

Co-authored papers 5

Deborah A Nickerson

University of Washington

Co-authored papers 4

Santhosh Girirajan

The Huck Institutes of Life Sciences, University Park, Pennsylvania State University

Co-authored papers 3

Evan E Eichler

University of Washington

Co-authored papers 2

Elizabeth E Blue

University of Washington

Co-authored papers 2

Chang-En Yu

and Clinical Center

Co-authored papers 2

Ian B Stanaway

Kidney Research Institute and Division of Nephrology, University of Washington

Co-authored papers 2

Hilary Coon

Co-authored papers 2

Mark J Rieder

Co-authored papers 1

Christophe L M J Verlinde

University of Washington

Co-authored papers 1

Kostantin Kiianitsa

University of Washington

Co-authored papers 1

Giovanni Battista Ferrero

Co-authored papers 1

Gerard D Schellenberg

Co-authored papers 1

James B Leverenz

Lou Ruvo Center for Brain Health, Cleveland Clinic

Co-authored papers 1

Eric J Topol

Universidade Federal de Sao Paulo

Co-authored papers 1

Andrew B Singleton

National Institute on Aging

Co-authored papers 1

Dong-Hui Chen

University of Washington School of Medicine

Co-authored papers 1

Lindsay A Farrer

Boston University Chobanian & Avedisian School of Medicine

Co-authored papers 1

David S Carrell

Kaiser Permanente Washington Health Research Institute

Co-authored papers 1

Malia Rumbaugh

Indiana University School of Medicine

Co-authored papers 1

Margaret A Pericak-Vance

Co-authored papers 1

Maynard V Olson

University of Washington

Co-authored papers 1

Michael O Dorschner

University of Washington

Co-authored papers 1

Sevilla D Detera-Wadleigh

National Institute of Mental Health Intramural Research Program

Co-authored papers 1

Alison M Goate

Icahn School of Medicine at Mount Sinai

Co-authored papers 1

Ji Eun Lee

Soonchunhyang University College of Medicine, Bucheon Hospital

Co-authored papers 1

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