(Q57840221)

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Molecular characterization of an interstitial deletion of 1p31.3 in a patient with obesity and psychiatric illness and a review of the literature

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Europe PubMed Central

Molecular characterization of an interstitial deletion of 1p31.3 in a patient with obesity and psychiatric illness and a review of the literature (English)

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Bernice E. Morrow

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Bernice Morrow

7

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Sadaf Farooqi

6

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author name string

Marilena Petti

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Joy Samanich

2

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Qiulu Pan

3

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Chih-Kang Huang

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Jana Reinmund

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Melanie Babcock

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language of work or name

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publication date

17 March 2011

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American Journal of Medical Genetics

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155

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4

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825-832

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Clinical utility of contemporary molecular cytogenetics

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Transmitted cytogenetic abnormalities in patients with mental retardation: pathogenic or normal variants?

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Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

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Complex balanced translocation t(1;5;7)(p32.1;q14.3;p21.3) and two microdeletions del(1)(p31.1p31.1) and del(7)(p14.1p14.1) in a patient with features of Greig cephalopolysyndactyly and mental retardation.

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Disrupted in Schizophrenia 1 and Nudel form a neurodevelopmentally regulated protein complex: implications for schizophrenia and other major neurological disorders

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Disrupted in Schizophrenia 1 Interactome: evidence for the close connectivity of risk genes and a potential synaptic basis for schizophrenia

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Behavioral phenotypes of Disc1 missense mutations in mice

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A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction

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The cyclic AMP system and Drosophila learning.

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Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor

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PDE4B polymorphisms and decreased PDE4B expression are associated with schizophrenia

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Anatomic localization of alternatively spliced leptin receptors (Ob-R) in mouse brain and other tissues.

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Leptin and the regulation of body weight in mammals

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Two cases of interstitial deletion 1p

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Abnormal splicing of the leptin receptor in diabetic mice

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Localization of leptin receptor mRNA and the long form splice variant (Ob-Rb) in mouse hypothalamus and adjacent brain regions by in situ hybridization

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DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling

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Disrupted in schizophrenia 1 and phosphodiesterase 4B: towards an understanding of psychiatric illness

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Interstitial deletion of the short arm of chromosome 1: attempt to establish a clinical phenotype (46,XX,del (1)(p22p32)).

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Autosomal genomic scan for loci linked to obesity and energy metabolism in Pima Indians

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Gene expression and association analyses of the phosphodiesterase 4B (PDE4B) gene in major depressive disorder in the Japanese population.

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Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding

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Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases.

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Behavioral and neurochemical characterization of mice deficient in the phosphodiesterase-4B (PDE4B) enzyme.

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Identification and expression cloning of a leptin receptor, OB-R

1 reference

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Dysregulation of the adipoinsular axis -- a mechanism for the pathogenesis of hyperleptinemia and adipogenic diabetes induced by fetal programming.

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10.1002/AJMG.A.33869

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