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Items: 13


Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.

Angulo MA, Butler MG, Cataletto ME.

J Endocrinol Invest. 2015 Dec;38(12):1249-63. doi: 10.1007/s40618-015-0312-9. Epub 2015 Jun 11. Review.


Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromes.

Butler MG, Wang K, Marshall JD, Naggert JK, Rethmeyer JA, Gunewardena SS, Manzardo AM.

Adv Genomics Genet. 2015;2015(5):53-75.


Differences between the pattern of developmental abnormalities in autism associated with duplications 15q11.2-q13 and idiopathic autism.

Wegiel J, Schanen NC, Cook EH, Sigman M, Brown WT, Kuchna I, Nowicki K, Wegiel J, Imaki H, Ma SY, Marchi E, Wierzba-Bobrowicz T, Chauhan A, Chauhan V, Cohen IL, London E, Flory M, Lach B, Wisniewski T.

J Neuropathol Exp Neurol. 2012 May;71(5):382-97. doi: 10.1097/NEN.0b013e318251f537.


12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes.

Youngs EL, Henkhaus RS, Hellings JA, Butler MG.

Clin Dysmorphol. 2012 Apr;21(2):93-6. doi: 10.1097/MCD.0b013e32834e9216. No abstract available.


Genetic variants and monoallelic expression of surfactant protein-D in inflammatory bowel disease.

Lin Z, John G, Hegarty JP, Berg A, Yu W, Wang Y, Kelly AA, Peterson BZ, Poritz LS, Floros J, Koltun WA.

Ann Hum Genet. 2011 Sep;75(5):559-68. doi: 10.1111/j.1469-1809.2011.00662.x. Epub 2011 Jul 25.


Gene expression in cardiac tissues from infants with idiopathic conotruncal defects.

Bittel DC, Butler MG, Kibiryeva N, Marshall JA, Chen J, Lofland GK, O'Brien JE Jr.

BMC Med Genomics. 2011 Jan 5;4:1. doi: 10.1186/1755-8794-4-1.


Somatosensory and sensorimotor consequences associated with the heterozygous disruption of the autism candidate gene, Gabrb3.

DeLorey TM, Sahbaie P, Hashemi E, Li WW, Salehi A, Clark DJ.

Behav Brain Res. 2011 Jan 1;216(1):36-45. doi: 10.1016/j.bbr.2010.06.032. Epub 2010 Aug 10.


Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15.

Sharp AJ, Migliavacca E, Dupre Y, Stathaki E, Sailani MR, Baumer A, Schinzel A, Mackay DJ, Robinson DO, Cobellis G, Cobellis L, Brunner HG, Steiner B, Antonarakis SE.

Genome Res. 2010 Sep;20(9):1271-8. doi: 10.1101/gr.108597.110. Epub 2010 Jul 14.


Analysis of the Prader-Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) array.

Newkirk HL, Bittel DC, Butler MG.

Am J Med Genet A. 2008 Sep 15;146A(18):2346-54. doi: 10.1002/ajmg.a.32459.


Immunologic and neurodevelopmental susceptibilities of autism.

Pessah IN, Seegal RF, Lein PJ, LaSalle J, Yee BK, Van De Water J, Berman RF.

Neurotoxicology. 2008 May;29(3):532-45. doi: 10.1016/j.neuro.2008.02.006. Epub 2008 Feb 23. Review.


15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders.

Hogart A, Nagarajan RP, Patzel KA, Yasui DH, Lasalle JM.

Hum Mol Genet. 2007 Mar 15;16(6):691-703. Epub 2007 Mar 5.


Whole genome microarray analysis of gene expression in Prader-Willi syndrome.

Bittel DC, Kibiryeva N, Sell SM, Strong TV, Butler MG.

Am J Med Genet A. 2007 Mar 1;143A(5):430-42.


Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome.

Bittel DC, Kibiryeva N, McNulty SG, Driscoll DJ, Butler MG, White RA.

Am J Med Genet A. 2007 Mar 1;143A(5):422-9.

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