Zoran Brkanac

2.8k citations

32 papers · 1.6k indexed · h-index 24

Molecular Biology top 10%
Genetics top 5%
Cellular and Molecular Neuroscience top 5%
Developmental and Educational Psychology top 5%
Cognitive Neuroscience top 5%

Co-authors: Wendy H. Raskind Mark Matsushita Ellen M. Wijsman Robin J. Leach Virginia W. Berninger Jannine D. Cody Raphael Bernier Tiffany Vu
Topics: Genetics and Neurodevelopmental Disorders (13 papers)Genomic variations and chromosomal abnormalities (9 papers)Reading and Literacy Development (6 papers)
Cited by: Developmental and Educational Psychology Genetics Cellular and Molecular Neuroscience
Journals: Bioinformatics PLoS ONE The American Journal of Human Genetics
Partner nations: United States Germany Italy

In The Last Decade

Zoran Brkanac

32 papers receiving 1.6k citations

Peers

Countries citing papers authored by Zoran Brkanac

Since Specialization

Citations

This map shows the geographic impact of Zoran Brkanac's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Zoran Brkanac with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Zoran Brkanac more than expected).

Fields of papers citing papers by Zoran Brkanac

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Zoran Brkanac. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Zoran Brkanac. The network helps show where Zoran Brkanac may publish in the future.

Co-authorship network of co-authors of Zoran Brkanac

This figure shows the co-authorship network connecting the top 25 collaborators of Zoran Brkanac. A scholar is included among the top collaborators of Zoran Brkanac based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Zoran Brkanac. Zoran Brkanac is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism 2016 ·Molecular Psychiatry ·Moran Rubinstein,Ashok Patowary,Ian B. Stanaway,(unknown),Ryan Nesbitt,(unknown),Todd Scheuer,Deborah A. Nickerson,Wendy H. Raskind,Ellen M. Wijsman,R. Bernier,William A. Catterall,Zoran Brkanac	29
2	Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes 2015 ·Human Genetics ·Nicola H. Chapman,Alejandro Q. Nato,Raphael Bernier,Katy Ankenman,Harkirat Sohi,Jeff Munson,Ashok Patowary,(unknown),Elizabeth Blue,Sara Jane Webb,Hilary Coon,Wendy H. Raskind,Zoran Brkanac,Ellen M. Wijsman	42
3	Identification of Rare Variants from Exome Sequence in a Large Pedigree with Autism 2012 ·Human Heredity ·Elizabeth E. Marchani,N.H. Chapman,Christina Cheung,Katy Ankenman,Ian B. Stanaway,Hilary Coon,Deborah A. Nickerson,R. Bernier,Zoran Brkanac,Ellen M. Wijsman	9
4	Evidence for involvement of GNB1L in autism 2011 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·(unknown),Mark Matsushita,Santhosh Girirajan,(unknown),(unknown),Youngmee Sul,Raphael Bernier,Annette Estes,Géraldine Dawson,Nancy J. Minshew,(unknown),Evan E. Eichler,Mark J. Rieder,Deborah A. Nickerson,Debby W. Tsuang,Ming T. Tsuang,Ellen M. Wijsman,Wendy H. Raskind,Zoran Brkanac	21
5	Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample 2010 ·Journal of Neurodevelopmental Disorders ·Beate Peter,Wendy H. Raskind,Mark Matsushita,(unknown),Tiffany Vu,Virginia W. Berninger,Ellen M. Wijsman,Zoran Brkanac	88
6	The Effect of Algorithms on Copy Number Variant Detection 2010 ·PLoS ONE ·Debby W. Tsuang,Steven P. Millard,Benjamin A. Ely,Peter Chi,(unknown),Wendy H. Raskind,(unknown),Zoran Brkanac,Chang Yu	27
7	IFRD1 Is a Candidate Gene for SMNA on Chromosome 7q22-q23 2009 ·The American Journal of Human Genetics ·Zoran Brkanac,David H. Spencer,Jay Shendure,Peggy D. Robertson,Mark Matsushita,Tiffany Vu,Thomas D. Bird,Maynard V. Olson,Wendy H. Raskind	35
8	Genome Scan of a Nonword Repetition Phenotype in Families with Dyslexia: Evidence for Multiple Loci 2008 ·Behavior Genetics ·Zoran Brkanac,Nicola H. Chapman,Robert P. Igo,Mark Matsushita,Kathleen Nielsen,Virginia W. Berninger,Ellen M. Wijsman,Wendy H. Raskind	26
9	Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia 2007 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Zoran Brkanac,Nicola H. Chapman,Mark Matsushita,(unknown),Kathleen Nielsen,Elizabeth Cochrane,Virginia W. Berninger,Ellen M. Wijsman,Wendy H. Raskind	78
10	A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency 2005 ·Molecular Psychiatry ·Wendy H. Raskind,Robert P. Igo,N.H. Chapman,Virginia W. Berninger,Jennifer B. Thomson,Megumi Matsushita,Zoran Brkanac,Ted Holzman,Matthew Brown,Ellen M. Wijsman	58
11	Genomewide scan for real‐word reading subphenotypes of dyslexia: Novel chromosome 13 locus and genetic complexity 2005 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Robert P. Igo,Nicola H. Chapman,Virginia W. Berninger,Mark Matsushita,Zoran Brkanac,Joseph H. Rothstein,Ted Holzman,Kathleen Nielsen,Wendy H. Raskind,Ellen M. Wijsman	39
12	Linkage analyses of four regions previously implicated in dyslexia: Confirmation of a locus on chromosome 15q 2004 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Nicola H. Chapman,Robert P. Igo,Jennifer B. Thomson,Mark Matsushita,Zoran Brkanac,Ted Holzman,Virginia W. Berninger,Ellen M. Wijsman,Wendy H. Raskind	73
13	Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia 2003 ·The American Journal of Human Genetics ·Dong-Hui Chen,Zoran Brkanac,Christophe L. M. J. Verlinde,(unknown),(unknown),David Nochlin,Mark Matsushita,Hillary Lipe,John Wolff,Magali Fernandez,Patrick J. Cimino,(unknown),Wendy H. Raskind	174
14	A New Dominant Spinocerebellar Ataxia Linked to Chromosome 19q13.4-qter 2002 ·Archives of Neurology ·Zoran Brkanac,(unknown),Magali Fernandez,Mark Matsushita,Hillary Lipe,John Wolff,David Nochlin,Wendy H. Raskind,Thomas D. Bird	53
15	Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22‐q32 2002 ·American Journal of Medical Genetics ·Zoran Brkanac,Magali Fernandez,Mark Matsushita,(unknown),John Wolff,Thomas D. Bird,Wendy H. Raskind	47
16	Genetic pattern of prostate cancer progression 1999 ·International Journal of Cancer ·Tomo Šarić,Zoran Brkanac,Dean A. Troyer,Susan S. Padalecki,Michael Sarosdy,Kenneth Williams,(unknown),Robin J. Leach,P. O’Connell	61
17	Evidence for a Novel Osteosarcoma Tumor-Suppressor Gene in the Chromosome 18 Region Genetically Linked with Paget Disease of Bone 1998 ·The American Journal of Human Genetics ·Maggie Nellissery,Susan S. Padalecki,Zoran Brkanac,Frederick R. Singer,G. David Roodman,K. Krishnan Unni,Robin J. Leach,Marc F. Hansen	82
18	Identification of Cryptic Rearrangements in Patients with 18q− Deletion Syndrome 1998 ·The American Journal of Human Genetics ·Zoran Brkanac,Jannine D. Cody,Robin J. Leach,Barbara R. DuPont	40
19	Preferential loss of the paternal alleles in the 18q- syndrome 1997 ·American Journal of Medical Genetics ·Jannine D. Cody,(unknown),Zoran Brkanac,Rosemarie Plaetke,Patricia D. Ghidoni,Celia I. Kaye,Robin J. Leach	65
20	Assignment of the Human Nuclear Hormone Receptor, NUC1 (PPARD), to Chromosome 6p21.1–p21.2 1996 ·Genomics ·Takeo Yoshikawa,Zoran Brkanac,Barbara R. DuPont,Guoqiang Xing,Robin J. Leach,S D Detera-Wadleigh	33

About Zoran Brkanac

Zoran Brkanac is a scholar working on Genetics, Developmental and Educational Psychology and Statistics and Probability, having authored 32 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (13 papers), Genomic variations and chromosomal abnormalities (9 papers) and Reading and Literacy Development (6 papers). The work is most often cited by research in Developmental and Educational Psychology (306 citations), Genetics (675 citations) and Cellular and Molecular Neuroscience (332 citations). Zoran Brkanac has collaborated with scholars based in United States, Germany and Italy. Frequent co-authors include Wendy H. Raskind, Mark Matsushita, Ellen M. Wijsman, Robin J. Leach, Virginia W. Berninger, Jannine D. Cody, Raphael Bernier, Tiffany Vu, Nicola H. Chapman and Magali Fernandez. Their work appears in journals such as Bioinformatics, PLoS ONE and The American Journal of Human Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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