LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

Molecular Psychiatry

Volumn 12, Issue 12, 2007, Pages 1129-1139

  Francks, C ^a,b   Maegawa, S ^c   Lauren J ^d   Abrahams, B S ^e   Velayos Baeza, A ^a   Medland, S E ^f,g   Colella, S ^a   Groszer, M ^a   McAuley, E Z ^a   Caffrey, T M ^a   Timmusk, T ^h   Pruunsild, P ^h   Koppel, I ^h   Lind, P A ^g   Matsumoto Itaba, N ⁱ   Nicod, J ^a   Xiong, L ^j   Joober, R ^k   Enard, W ^l   Krinsky, B ^l   Nanba, E ^c   Richardson, A J ^m   Riley, B P ^e   Martin, N G ^f   Strittmatter, S M ^d   Moller H J ⁿ   Rujescu, D ⁿ   St Clair, D ^o   Muglia, P ^b   Roos, J L ^p   Fisher, S E ^a   Wade Martins, R ^a   Rouleau, G A ^j   Stein, J F ^m   Karayiorgou, M ^q   Geschwind, D H ^e   Ragoussis, J ^a   Kendler, K S ^e   Airaksinen, M S ^r   Oshimura, M ⁱ   Delisi, L E ^s,t   Monaco, A P ^a   more..

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b GSK   (Italy)

^c TOTTORI UNIVERSITY   (Japan)

^d YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e UNIVERSITY OF CALIFORNIA   (United States)

^f VIRGINIA COMMONWEALTH UNIVERSITY   (United States)

^g QIMR BERGHOFER MEDICAL RESEARCH INSTITUTE   (Australia)

^h TALLINN UNIVERSITY OF TECHNOLOGY   (Estonia)

ⁱ TOTTORI UNIVERSITY   (Japan)

^j CENTRE HOSPITALIER DE L UNIVERSITÉ DE MONTRÉAL   (Canada)

^k MCGILL UNIVERSITY   (Canada)

^l MAX PLANCK INSTITUTE FOR EVOLUTIONARY ANTHROPOLOGY   (Germany)

^m UNIVERSITY OF OXFORD   (United Kingdom)

ⁿ LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^o UNIVERSITY OF ABERDEEN   (United Kingdom)

^p UNIVERSITY OF PRETORIA   (South Africa)

^q ROCKEFELLER UNIVERSITY   (United States)

^r UNIVERSITY OF HELSINKI   (Finland)

^s NEW YORK UNIVERSITY   (United States)

^t NATHAN S KLINE INSTITUTE FOR PSYCHIATRIC RESEARCH   (United States)

more..

Author keywords

Association; Brain asymmetry; Handedness; Imprinted gene; Schizophrenia

Indexed keywords

LEUCINE RICH REPEAT TRANSMEMBRANE NEURONAL 1; MEMBRANE PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; BEHAVIOR; BRAIN ASYMMETRY; CHROMOSOME 2P; COGNITION; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; DISEASE TRANSMISSION; DOWN REGULATION; DYSLEXIA; FAMILY; FOREBRAIN; GENE EXPRESSION; GENE REPRESSION; GENETICS; GENOME IMPRINTING; HANDEDNESS; HAPLOTYPE; HUMAN; NERVE CELL DIFFERENTIATION; PATERNALISM; PRIORITY JOURNAL; PROTEIN EXPRESSION; QUANTITATIVE ANALYSIS; SCHIZOPHRENIA;

ANIMALS; BRAIN; CELL LINE, TRANSFORMED; CHROMOSOMES, HUMAN, PAIR 2; FAMILY HEALTH; FEMALE; FUNCTIONAL LATERALITY; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION; KARYOTYPING; MALE; MEMBRANE PROTEINS; MICE; NERVE TISSUE PROTEINS; SCHIZOPHRENIA; SUBCELLULAR FRACTIONS;

EID: 36549060114     PISSN: 13594184     EISSN: 14765578     Source Type: Journal    
DOI: 10.1038/sj.mp.4002053     Document Type: Article

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