Zoran Brkanac

PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers

Alejandro Q. Nato, Nicola H. Chapman, Ellen M. Wijsman, 2015, Bioinform..

Suppression and facilitation of human neural responses

Michael-Paul Schallmo, Rachel Millin, Scott O Murray, 2017, bioRxiv.

Suppression and facilitation of human neural responses

Michael-Paul Schallmo, Scott O. Murray, Anastasia V. Flevaris, 2017 .

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

Ellen M Wijsman, Zoran Brkanac, Virginia W Berninger, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes

Carlos S. Moreno, Carl Baker, Evan E. Eichler, 2011, PLoS genetics.

Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia.

Zoran Brkanac, David Nochlin, C. Verlinde, 2003, American journal of human genetics.

Genetic Determinants of Addiction to Opioids and Cocaine

Zoran Brkanac, M. Oreskovich, A. Saxon, 2005, Harvard review of psychiatry.

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

Ellen M. Wijsman, Virginia W. Berninger, Beate Peter, 2010, Journal of Neurodevelopmental Disorders.

Genomewide scan for real‐word reading subphenotypes of dyslexia: Novel chromosome 13 locus and genetic complexity

Ellen M Wijsman, Robert P Igo, Zoran Brkanac, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.