Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes-Reference-Cited by-同舟云学术

Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes

Published:2018-05-11 Issue:7 Volume:39 Page:939-946
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Grochowski Christopher M.¹,Gu Shen¹,Yuan Bo¹,TCW Julia²³,Brennand Kristen J.²,Sebat Jonathan⁴,Malhotra Dheeraj⁵,McCarthy Shane⁶,Rudolph Uwe⁷⁸,Lindstrand Anna⁹¹⁰,Chong Zechen¹¹,Levy Deborah L.⁸¹²,Lupski James R.¹¹³¹⁴¹⁵,Carvalho Claudia M.B.¹^ORCID

Affiliation:

1. Department of Molecular and Human Genetics; Baylor College of Medicine; Houston Texas

2. Department of Neuroscience; Friedman Brain Institute, Icahn School of Medicine at Mount Sinai; New York New York

3. Ronald M. Loeb Center for Alzheimer's Disease; Icahn School of Medicine at Mount Sinai; New York New York

4. Beyster Center for Psychiatric Genomics, Department of Psychiatry; University of California at San Diego; San Diego California

5. Hoffmann-La Roche Ltd; Basel Switzerland

6. Cold Spring Harbor Laboratory; Cold Spring Harbor; New York

7. Laboratory of Genetic Neuropharmacology; McLean Hospital; Belmont Massachusetts

8. Department of Psychiatry; Harvard Medical School; Boston Massachusetts

9. Department of Molecular Medicine and Surgery; Karolinska Institutet; Stockholm Sweden

10. Department of Clinical Genetics; Karolinska University Hospital; Stockholm Sweden

11. Department of Genetics and the Informatics Institute; The University of Alabama at Birmingham; Birmingham Alabama

12. Psychology Research Laboratory; McLean Hospital; Belmont Massachusetts

13. Human Genome Sequencing Center; Baylor College of Medicine; Houston Texas

14. Department of Pediatrics; Baylor College of Medicine; Houston Texas

15. Texas Children's Hospital; Houston Texas

Funder

National Institute of Neurological Disorders and Stroke

National Institutes of Health

National Institute of General Medical Sciences

Anonymous Foundation

Ellison Foundation

Team Daniel

Carmela and Menachem Abraham Fund

Stanley Foundation

Uppmax Project

New York Stem Cell Foundation

National Human Genome Research Institute

National Institute of Mental Health

Royal Physiographic Society

SciLifeLab National Sequencing Project

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference42 articles.

1. A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: Genotype-phenotype correlation;Abu-Amero;BMC Medical Genetics,2010

2. Small supernumerary marker chromosome may provide information on dosage-insensitive pericentric regions in human;Al-Rikabi;Current Genomics,2018

3. Complex genomic rearrangements at the PLP1 locus include triplication and quadruplication;Beck;PLoS Genetics,2015

4. Parental somatic mosaicism is underrecognized and influences recurrence risk of genomic disorders;Campbell;American Journal of Human Genetics,2014

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