Andrew Zinn, M.D., Ph.D.
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RELEVANT PUBLICATIONS

Tolson KP, Gemelli T, Meyer D, Yazdani U, Kozlitina J, Zinn AR. (2014) Inducible neuronal inactivation of Sim1 in adult mice causes hyperphagic obesity. Endocrinology. en20132125. PMID: 24773343

Heymsfield SB, Avena NM, Baier L, Brantley P, Bray GA, Burnett LC, Butler MG, Driscoll DJ, Egli D, Elmquist J, Forster JL, Goldstone AP, Gourash LM, Greenway FL, Han JC, Kane JG, Leibel RL, Loos RJ, Scheimann AO, Roth CL, Seeley RJ, Sheffield V, Tauber M, Vaisse C, Wang L, Waterland RA, Wevrick R, Yanovski JA, Zinn AR. (2014) Hyperphagia: current concepts and future directions proceedings of the 2nd international conference on hyperphagia. Obesity (Silver Spring). 22 Suppl 1:S1-S17.

Harrison SM, Campbell IM, Keays M, Granberg CF, Villanueva C, Tannin G, Zinn AR, Castrillon DH, Shaw CA, Stankiewicz P, Baker LA. (2013) Screening and familial characterization of copy-number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure. Am J Med Genet A. 161(10):2487-94.

Ross JL, Roeltgen DP, Kushner H, Zinn AR, Reiss A, Bardsley MZ, McCauley E, Tartaglia N. (2012) Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome. Pediatrics. 129(4):769-78.

Payne AR, Chang SW, Koenig SN, Zinn AR, Garg V. (2012) Submicroscopic chromosomal copy number variations identified in children with hypoplastic left heart syndrome. Pediatr Cardiol. 33(5):757-63.

Bhoj EJ, Ramos P, Baker LA, Garg V, Cost N, Nordenskjöld A, Elder FF, Bleyl SB, Bowles NE, Arrington CB, Delhomme B, Vanhoutteghem A, Djian P, Zinn AR. (2011) Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development. Eur J Hum Genet. 19(5):540-6.

Benito-Sanz S, Barroso E, Heine-Suñer D, Hisado-Oliva A, Romanelli V, Rosell J, Aragones A, Caimari M, Argente J, Ross JL, Zinn AR, Gracia R, Lapunzina P, Campos-Barros A, Heath KE. (2011) Clinical and molecular evaluation of SHOX/PAR1 duplications in Leri-Weill dyschondrosteosis (LWD) and idiopathic short stature (ISS). J Clin Endocrinol Metab. 96(2):E404-12.

de Leeuw N, Bulk S, Green A, Jaeckle-Santos L, Baker LA, Zinn AR, Kleefstra T, van der Smagt JJ, Vianne Morgante AM, de Vries BB, van Bokhoven H, de Brouwer AP. (2010) UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients. Am J Med Genet A. 152A(12):3084-90

Xu Y, Jones JE, Lauzon DA, Anderson JG, Balthasar N, Heisler LK, Zinn AR, Lowell BB, Elmquist JK. (2010) A serotonin and melanocortin circuit mediates D-fenfluramine anorexia. J Neurosci. 30(44):14630-4.

Irani BG, Donato J Jr, Olson DP, Lowell BB, Sacktor TC, Reyland ME, Tolson KP, Zinn AR, Ueta Y, Sakata I, Zigman JM, Elias CF, Clegg DJ. (2010) Distribution and neurochemical characterization of protein kinase C-theta and -delta in the rodent hypothalamus. Neuroscience 170(4):1065-79

Tolson KP, Gemelli T, Gautron L, Elmquist JK, Zinn AR* and Kublaoui BM*. (*Equal contributors.) 2010. Postnatal Sim1 deficiency causes hyperphagic obesity and reduced Mc4r and Oxytocin expression. J. Neurosci 30:3803.

Kublaoui BM, Gemelli T, Tolson KP, Wang Y, Zinn AR. 2008. Oxytocin deficiency mediates hyperphagic obesity of Sim1 haploinsufficient mice. Mol Endocrinol 22:.1723-1734. PMCID: 2453606

Kublaoui BM, Holder JL Jr, Gemelli T, Zinn AR. 2006. Sim1 haploinsufficiency impairs melanocortin-mediated anorexia and activation of paraventricular nucleus neurons. Mol Endocrinol 20:2483-2492.

Kublaoui BM, Holder JL Jr, Tolson KP, Gemelli T, Zinn AR. 2006. SIM1 overexpression partially rescues agouti yellow and diet-induced obesity by normalizing food intake. Endocrinology 147:4542-4549.

Holder Jr JL, Zhang L, Kublaoui BM, DiLeone RJ, Oz OK, Bair CH, Lee YH, and Zinn AR. 2004. Sim1 gene dosage modulates the homeostatic feeding response to increased dietary fat in mice. Am J Physiol Endocrinol Metab 287, E105-13.

Holder JL, Butte NF, and Zinn AR  2000. Profound obesity associated with a balanced translocation that disrupts the SIM1 gene. Hum Mol Gen 9:101-8.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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