Molecular Genetics & Genomic Medicine is a peer-reviewed journal for rapid dissemination of quality research related to the dynamically developing areas of human, molecular and medical genetics. The journal publishes original research articles covering findings in phenotypic, molecular, biological, and genomic aspects of genomic variation, inherited disorders and birth defects. The broad publishing spectrum of Molecular Genetics & Genomic Medicine includes rare and common disorders from diagnosis to treatment. Examples of appropriate articles include reports of novel disease genes, functional studies of genetic variants, in-depth genotype-phenotype studies, genomic analysis of inherited disorders, molecular diagnostic methods, medical bioinformatics, ethical, legal, and social implications (ELSI), and approaches to clinical diagnosis. Molecular Genetics & Genomic Medicine provides a scientific home for next generation sequencing studies of rare and common disorders, which will make research in this fascinating area easily and rapidly accessible to the scientific community. This will serve as the basis for translating next generation sequencing studies into individualized diagnostics and therapeutics, for day-to-day medical care.
Molecular Genetics & Genomic Medicine publishes original research articles, reviews, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented.

EDITOR-IN-CHIEF
(USA)Suzanne Hart* (National Human Genome Research Institute, NIH, Bethesda, Maryland, USA; Email: MGGM@wiley.com)

*Dr. Hart serves in her own capacity




ASSOCIATE EDITORS
(USA)Paul Kruszka* (National Human Genome Research Institute, NIH, Bethesda, Maryland, USA)

(Hong Kong)Wanling Yang (University of Hong Kong, Hong Kong SAR, P.R. China)

(USA)Yingze Zhang (University of Pittsburgh, Pennsylvania, USA)

*Dr. Kruszka serves in his own capacity




FOUNDING EDITOR
(USA)Maximilian Muenke* (National Human Genome Research Institute, NIH, Bethesda, Maryland, USA)

*Dr. Muenke serves in his own capacity




EDITORIAL BOARD
(Sweden)Eleni Aklillu (Karolinska Institutet, Sweden)

(Saudi Arabia)Fowzan S. Alkuraya (College of Medicine, Alfaisal University, Saudi Arabia)

(Israel)Yair Anikster (Sheba Medical Center, Israel)

(Colombia)Mauricio Arcos-Burgos (Universidad del Rosario, Colombia)

(Turkey)Nurten A. Akarsu (Hacetepe University, Turkey)

(USA)Michael Bamshad (University of Washington School of Medicine, USA)

(Canada)Kym Boycott (Children's Hospital of Eastern Ontario and University of Ottawa, Canada)

(Chile)María Leonor Bustamente Calderón (University of Chile, Chile)

(Canada)Ronald D. Cohn (University of Toronto, Canada)

(France)Véronique David (University of Rennes, France)

(USA)Mauricio De Castro (Air Force Medical Genetics Center, USA)

(USA)Michael J. Gambello (Emory University, USA)

(USA)Andrea Gropman (Children's National Medical Center, USA)

(USA)Ophir Klein (University of California, San Francisco, USA)

(UK)Robert Kleta (University College London, United Kingdom)

(Czech Republic)Stanislav Kmoch (Charles University in Prague, Czech Republic)

(Brazil)Maria Rita Passos-Bueno (University of Sao Paulo, Brazil)

(India)Shubha R. Phadke (Sanjay Gandhi Postgraduate Institute of Medical Sciences, India)

(Singapore)Bruno Reversade (A*STAR, Singapore)

(USA)Lisa A. Schimmenti (Mayo Clinic, USA)

(Thailand)Vorasuk Shotelersuk (Chulalongkorn University, Thailand)

(USA)Anne Slavotinek (University of California, San Francisco, USA)

(The Netherlands)Joris Veltman (Radboud University Nijmegen Medical Centre, The Netherlands)

(Germany)Bernd Wollnik (Institute of Human Genetics Gottingen, Germany)