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Sex-chromosome dosage effects on gene expression in humans

Proceedings of the National Academy of Sciences - PNAS, 2018-07, Vol.115 (28), p.7398-7403

2018

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Oxytocin Deficiency Mediates Hyperphagic Obesity of Sim1 Haploinsufficient Mice

Molecular endocrinology (Baltimore, Md.), 2008-07, Vol.22 (7), p.1723-1734

2008

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Sim1 Haploinsufficiency Impairs Melanocortin-Mediated Anorexia and Activation of Paraventricular Nucleus Neurons

Molecular endocrinology (Baltimore, Md.), 2006-10, Vol.20 (10), p.2483-2492

2006

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Effect of Ascertainment and Genetic Features on the Phenotype of Klinefelter Syndrome

The Journal of pediatrics, 2008-05, Vol.152 (5), p.716-722

2008

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Dynamic regulation of p53 subnuclear localization and senescence by MORC3

Molecular biology of the cell, 2007-05, Vol.18 (5), p.1701-1709

2007

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Identification of 15 novel partial SHOX deletions and 13 partial duplications, and a review of the literature reveals intron 3 to be a hotspot region

Journal of human genetics, 2017-02, Vol.62 (2), p.229-234

2017

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SIM1 Overexpression Partially Rescues Agouti Yellow and Diet-Induced Obesity by Normalizing Food Intake

Endocrinology (Philadelphia), 2006-10, Vol.147 (10), p.4542-4549

2006

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Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome

Pediatrics (Evanston), 2012-04, Vol.129 (4), p.769

2012

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Computing power of quantitative trait locus association mapping for haploid loci

BMC bioinformatics, 2009-08, Vol.10 (1), p.261-261, Article 261

2009

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Postnatal Sim1 Deficiency Causes Hyperphagic Obesity and Reduced Mc4r and Oxytocin Expression

The Journal of neuroscience, 2010-03, Vol.30 (10), p.3803-3812

2010

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Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development

European journal of human genetics : EJHG, 2011-05, Vol.19 (5), p.540-546

2011

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A Turner syndrome neurocognitive phenotype maps to Xp22.3

Behavioral and brain functions, 2007-05, Vol.3 (1), p.24-24

2007

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Sim1 gene dosage modulates the homeostatic feeding response to increased dietary fat in mice

American journal of physiology: endocrinology and metabolism, 2004-07, Vol.287 (1), p.E105-E113

2004

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Inducible Neuronal Inactivation of Sim1 in Adult Mice Causes Hyperphagic Obesity

Endocrinology (Philadelphia), 2014-07, Vol.155 (7), p.2436-2444

2014

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UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients

American journal of medical genetics. Part A, 2010-12, Vol.152A (12), p.3084-3090

2010

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Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2019-10, Vol.180 (7), p.471-482

2019

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Sim1 Inhibits Bone Formation by Enhancing the Sympathetic Tone in Male Mice

Endocrinology (Philadelphia), 2015-04, Vol.156 (4), p.1408-1415

2015

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Hyperphagia: Current concepts and future directions proceedings of the 2nd international conference on hyperphagia

Obesity (Silver Spring, Md.), 2014-02, Vol.22 (S1), p.S1-S17

2014

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Unconventional Wisdom About the Obesity Epidemic

The American journal of the medical sciences, 2010-12, Vol.340 (6), p.481-491

ZINN, Andrew R

2010

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A serotonin and melanocortin circuit mediates D-fenfluramine anorexia

The Journal of neuroscience, 2010-11, Vol.30 (44), p.14630-14634

2010

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Androgen Receptor CAGn Repeat Length Influences Phenotype of 47,XXY (Klinefelter) Syndrome

The journal of clinical endocrinology and metabolism, 2005-09, Vol.90 (9), p.5041-5046

2005

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Cognitive and motor development during childhood in boys with Klinefelter syndrome

American journal of medical genetics. Part A, 2008-03, Vol.146A (6), p.708-719

2008

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Submicroscopic Chromosomal Copy Number Variations Identified in Children With Hypoplastic Left Heart Syndrome

Pediatric cardiology, 2012-06, Vol.33 (5), p.757-763

2012

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Profound obesity associated with a balanced translocation that disrupts the SIM1 gene

Human molecular genetics, 2000, Vol.9 (1), p.101-108

2000

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Sex-chromosome dosage effects on gene expression in humans

Oxytocin Deficiency Mediates Hyperphagic Obesity of Sim1 Haploinsufficient Mice

Sim1 Haploinsufficiency Impairs Melanocortin-Mediated Anorexia and Activation of Paraventricular Nucleus Neurons

Effect of Ascertainment and Genetic Features on the Phenotype of Klinefelter Syndrome

Dynamic regulation of p53 subnuclear localization and senescence by MORC3

Identification of 15 novel partial SHOX deletions and 13 partial duplications, and a review of the literature reveals intron 3 to be a hotspot region

SIM1 Overexpression Partially Rescues Agouti Yellow and Diet-Induced Obesity by Normalizing Food Intake

DNA polymerase-α regulates the activation of type I interferons through cytosolic RNA:DNA synthesis

Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome

Computing power of quantitative trait locus association mapping for haploid loci

Postnatal Sim1 Deficiency Causes Hyperphagic Obesity and Reduced Mc4r and Oxytocin Expression

Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development

A Turner syndrome neurocognitive phenotype maps to Xp22.3

Sim1 gene dosage modulates the homeostatic feeding response to increased dietary fat in mice

Inducible Neuronal Inactivation of Sim1 in Adult Mice Causes Hyperphagic Obesity

UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients

Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression

Sim1 Inhibits Bone Formation by Enhancing the Sympathetic Tone in Male Mice

Hyperphagia: Current concepts and future directions proceedings of the 2nd international conference on hyperphagia

Unconventional Wisdom About the Obesity Epidemic

A serotonin and melanocortin circuit mediates D-fenfluramine anorexia

Androgen Receptor CAGn Repeat Length Influences Phenotype of 47,XXY (Klinefelter) Syndrome

Cognitive and motor development during childhood in boys with Klinefelter syndrome

Submicroscopic Chromosomal Copy Number Variations Identified in Children With Hypoplastic Left Heart Syndrome

Profound obesity associated with a balanced translocation that disrupts the SIM1 gene

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