Andrew R Zinn

Andrew R Zinn

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Andrew R Zinn

Andrew R Zinn

Publications by authors named "Andrew R Zinn"

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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.

Am J Med Genet B Neuropsychiatr Genet 2019 Oct 3;180(7):471-482. Epub 2019 Jun 3.

McDermott Center for Human Growth and Development, UT Southwestern Medical Center, Dallas, Texas.

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http://dx.doi.org/10.1002/ajmg.b.32745DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6730649PMC
October 2019

Sex-chromosome dosage effects on gene expression in humans.

Proc Natl Acad Sci U S A 2018 07 26;115(28):7398-7403. Epub 2018 Jun 26.

Neurogenetics Program, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, CA 90095.

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http://dx.doi.org/10.1073/pnas.1802889115DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048519PMC
July 2018

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.

J Hum Genet 2017 Feb 8;62(2):229-234. Epub 2016 Sep 8.

Institute of Medical and Molecular Genetics (INGEMM), Hospital Universitario La Paz, Universidad Autónoma de Madrid, Madrid, Spain.

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http://dx.doi.org/10.1038/jhg.2016.113DOI Listing
February 2017

Sim1 inhibits bone formation by enhancing the sympathetic tone in male mice.

Endocrinology 2015 Apr 21;156(4):1408-15. Epub 2015 Jan 21.

Departments of Pharmacology (X.W., W.W., Y.W.) and Internal Medicine (A.R.Z.) and Eugene McDermott Center for Human Growth and Development (A.R.Z.), The University of Texas Southwestern Medical Center, Dallas, Texas 75390.

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http://dx.doi.org/10.1210/en.2014-1872DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4399315PMC
April 2015

Inducible neuronal inactivation of Sim1 in adult mice causes hyperphagic obesity.

Endocrinology 2014 Jul 28;155(7):2436-44. Epub 2014 Apr 28.

McDermott Center for Human Growth and Development (K.P.T., T.G., D.M., U.Y., J.K., A.R.Z.) and Department of Internal Medicine (A.R.Z.), The University of Texas Southwestern Medical Center, Dallas, Texas 75390-8591.

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http://dx.doi.org/10.1210/en.2013-2125DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060186PMC
July 2014

Submicroscopic chromosomal copy number variations identified in children with hypoplastic left heart syndrome.

Pediatr Cardiol 2012 Jun 21;33(5):757-63. Epub 2012 Feb 21.

Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

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http://link.springer.com/content/pdf/10.1007/s00246-012-0208
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http://link.springer.com/10.1007/s00246-012-0208-9
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http://dx.doi.org/10.1007/s00246-012-0208-9DOI Listing
June 2012

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

Pediatrics 2012 Apr 12;129(4):769-78. Epub 2012 Mar 12.

Department of Pediatrics, Thomas Jefferson University, Philadelphia, PA 19107, USA.

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http://dx.doi.org/10.1542/peds.2011-0719DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3356148PMC
April 2012

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

Eur J Hum Genet 2011 May 2;19(5):540-6. Epub 2011 Feb 2.

McDermott Center for Human Growth and Development and Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, TX, USA.

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http://dx.doi.org/10.1038/ejhg.2010.245DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3083624PMC
May 2011

Unconventional wisdom about the obesity epidemic.

Authors:
Andrew R Zinn

Am J Med Sci 2010 Dec;340(6):481-91

McDermott Center for Human Growth and Development and Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.

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http://dx.doi.org/10.1097/MAJ.0b013e3181ccb980DOI Listing
December 2010

An extra X or Y chromosome: contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome.

Dev Disabil Res Rev 2009 ;15(4):309-17

Department of Pediatrics, Thomas Jefferson University, 1025 Walnut Street, Suite 726, Philadelphia, PA 19107, USA.

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http://dx.doi.org/10.1002/ddrr.85DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2876236PMC
March 2010

Postnatal Sim1 deficiency causes hyperphagic obesity and reduced Mc4r and oxytocin expression.

J Neurosci 2010 Mar;30(10):3803-12

McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.

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http://dx.doi.org/10.1523/JNEUROSCI.5444-09.2010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3285557PMC
March 2010

Effect of growth hormone therapy on severe short stature and skeletal deformities in a patient with combined Turner syndrome and Langer mesomelic dysplasia.

J Clin Endocrinol Metab 2009 Dec 22;94(12):5028-33. Epub 2009 Oct 22.

Department of Pediatric Endocrinology, New York University Medical Center, 550 First Avenue, New York, New York 10016, USA.

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http://dx.doi.org/10.1210/jc.2009-0679DOI Listing
December 2009

Computing power of quantitative trait locus association mapping for haploid loci.

BMC Bioinformatics 2009 Aug 23;10:261. Epub 2009 Aug 23.

Department of Genetics, Rutgers University, 145 Bevier Road, Piscataway, NJ 08854, USA.

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http://dx.doi.org/10.1186/1471-2105-10-261DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2738682PMC
August 2009

MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetes.

Mol Cytogenet 2009 Feb 13;2. Epub 2009 Feb 13.

McDermott Center for Human Growth and Development, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.

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http://dx.doi.org/10.1186/1755-8166-2-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2646739PMC
February 2009

Oxytocin deficiency mediates hyperphagic obesity of Sim1 haploinsufficient mice.

Mol Endocrinol 2008 Jul 1;22(7):1723-34. Epub 2008 May 1.

Department of Pediatrics, Department of Internal Medicine, McDermott Center for Human Growth and Development, The University of Texas Southwestern Medical School, Dallas, TX 75390-8591, USA.

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http://dx.doi.org/10.1210/me.2008-0067DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2453606PMC
July 2008

EFHC2 SNP rs7055196 is not associated with fear recognition in 45,X Turner syndrome.

Am J Med Genet B Neuropsychiatr Genet 2008 Jun;147B(4):507-9

Department of Internal Medicine and McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

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http://dx.doi.org/10.1002/ajmg.b.30625DOI Listing
June 2008

Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes.

Hum Genet 2008 Jun 11;123(5):469-76. Epub 2008 Apr 11.

McDermott Center for Human Growth and Development, The University of Texas Southwestern Medical School, 5323 Harry Hines Boulevard, Dallas, TX 75390-8591, USA.

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http://dx.doi.org/10.1007/s00439-008-0498-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2714970PMC
June 2008

Effect of ascertainment and genetic features on the phenotype of Klinefelter syndrome.

J Pediatr 2008 May 21;152(5):716-22. Epub 2007 Dec 21.

Department of Pediatrics, Thomas Jefferson University, Philadelphia, PA 19107, USA.

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http://dx.doi.org/10.1016/j.jpeds.2007.10.019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6728163PMC
May 2008

Cognitive and motor development during childhood in boys with Klinefelter syndrome.

Am J Med Genet A 2008 Mar;146A(6):708-19

Department of Pediatrics, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

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http://dx.doi.org/10.1002/ajmg.a.32232DOI Listing
March 2008

Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's disease.

J Pediatr Surg 2007 Nov;42(11):1928-32

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9110, USA.

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http://dx.doi.org/10.1016/j.jpedsurg.2007.07.030DOI Listing
November 2007

The physical phenotype of girls and women with Turner syndrome is not X-imprinted.

Hum Genet 2007 May 23;121(3-4):469-74. Epub 2007 Jan 23.

Chief Developmental Endocrinology Branch, National Institute of Child Health, NIH, Bethesda, MD 20982, USA.

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http://dx.doi.org/10.1007/s00439-007-0324-4DOI Listing
May 2007

Dynamic regulation of p53 subnuclear localization and senescence by MORC3.

Mol Biol Cell 2007 May 1;18(5):1701-9. Epub 2007 Mar 1.

Department of Molecular Genetics and Molecular Biology, Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka, Osaka 537-8511, Japan.

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http://dx.doi.org/10.1091/mbc.e06-08-0747DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1855011PMC
May 2007

Compound heterozygosity of SHOX-encompassing and downstream PAR1 deletions results in Langer mesomelic dysplasia (LMD).

Am J Med Genet A 2007 May;143A(9):933-8

Department of Endocrinology, Hospital Infantil Universitario Niño Jesús, Universidad Autónoma de Madrid, Madrid, Spain.

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http://dx.doi.org/10.1002/ajmg.a.31676DOI Listing
May 2007

A Turner syndrome neurocognitive phenotype maps to Xp22.3.

Behav Brain Funct 2007 May 21;3:24. Epub 2007 May 21.

Eugene McDermott Center for Human Growth and Development and Department of Internal Medicine, The University of Texas Southwestern Medical School, Dallas TX, USA.

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http://dx.doi.org/10.1186/1744-9081-3-24DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1891305PMC
May 2007

Increased prevalence of ADHD in Turner syndrome with no evidence of imprinting effects.

J Pediatr Psychol 2006 Oct 8;31(9):945-55. Epub 2006 Mar 8.

Division of Human and Molecular Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, PA, USA.

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http://dx.doi.org/10.1093/jpepsy/jsj106DOI Listing
October 2006

SIM1 overexpression partially rescues agouti yellow and diet-induced obesity by normalizing food intake.

Endocrinology 2006 Oct 18;147(10):4542-9. Epub 2006 May 18.

Department of Pediatrics, and McDermott Center for Human Growth and Development, The University of Texas Southwestern Medical School, 5323 Harry Hines Boulevard, Dallas, 75390-8591, USA.

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http://dx.doi.org/10.1210/en.2006-0453DOI Listing
October 2006

Sim1 haploinsufficiency impairs melanocortin-mediated anorexia and activation of paraventricular nucleus neurons.

Mol Endocrinol 2006 Oct 25;20(10):2483-92. Epub 2006 May 25.

Department of Pediatrics, The University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390-8591, USA.

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http://dx.doi.org/10.1210/me.2005-0483DOI Listing
October 2006

Editorial: MC4R mutations--weight before screening!

J Clin Endocrinol Metab 2006 May;91(5):1671-2

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http://dx.doi.org/10.1210/jc.2006-0546DOI Listing
May 2006

X-linked reticulate pigmentary disorder with systemic manifestations: report of a third family and literature review.

Pediatr Dermatol 2005 Mar-Apr;22(2):122-6

Department of Dermatology, University of Texas Southwestern Medical School, Dallas, Texas 75390, USA.

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http://doi.wiley.com/10.1111/j.1525-1470.2005.22206.x
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http://dx.doi.org/10.1111/j.1525-1470.2005.22206.xDOI Listing
December 2005

Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndrome.

J Clin Endocrinol Metab 2005 Sep 14;90(9):5041-6. Epub 2005 Jun 14.

McDermott Center for Human Growth and Development, and Department of Internal Medicne, University of Texas Southwestern Medical School, 5323 Harry Hines Boulevard, Dallas, Texas 75390-8591, USA.

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http://dx.doi.org/10.1210/jc.2005-0432DOI Listing
September 2005

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

Am J Physiol Endocrinol Metab 2004 Jul 24;287(1):E105-13. Epub 2004 Feb 24.

Dept. of Internal Medicine, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-8591, USA.

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http://dx.doi.org/10.1152/ajpendo.00446.2003DOI Listing
July 2004

Mesomelic and rhizomelic short stature: The phenotype of combined Leri-Weill dyschondrosteosis and achondroplasia or hypochondroplasia.

Am J Med Genet A 2003 Jan;116A(1):61-5

Department of Pediatrics, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

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http://dx.doi.org/10.1002/ajmg.a.10807DOI Listing
January 2003

Complete SHOX deficiency causes Langer mesomelic dysplasia.

Am J Med Genet 2002 Jun;110(2):158-63

McDermott Center for Human Growth and Development and Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.

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http://doi.wiley.com/10.1002/ajmg.10422
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http://dx.doi.org/10.1002/ajmg.10422DOI Listing
June 2002