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Archives of Neurology|May 16, 2007
A new episodic ataxia syndrome with linkage to chromosome 19q13Kevin A Kerber, Joanna C Jen, Hane Lee, et al.
Frontiers in Psychiatry|December 19, 2013
Rare Genomic Variants Link Bipolar Disorder with Anxiety Disorders to CREB-Regulated Intracellular Signaling PathwaysBerit Kerner, Aliz R Rao, Bryce Christensen, et al.
Human Molecular Genetics|March 23, 2007
High density SNP association study of a major autism linkage region on chromosome 17Jennifer L Stone, Barry Merriman, Rita M Cantor, et al.
Nucleic Acids Research|May 19, 2026
Heterogeneous nuclear ribonucleoprotein A1 (hnRNPA1) maintains muscle progenitor identity by stabilizing the Ppp1r1b-lncRNA-PRC2 complexXuedong Kang, Yan Zhao, Stanley F Nelson, et al.
Biomarkers in Medicine|December 1, 2018
Cardiac MRI biomarkers for Duchenne muscular dystrophyPatrick Magrath, Nyasha Maforo, Pierangelo Renella, et al.
Headache|December 18, 2007
Phenotypic and genetic analysis of a large family with migraine-associated vertigoHane Lee, Joanna C Jen, Yoon-Hee Cha, et al.
Pediatric Blood & Cancer|September 28, 2012
Whole exome sequencing of pediatric gastric adenocarcinoma reveals an atypical presentation of Li-Fraumeni syndromeVivian Y Chang, Noah Federman, Julian Martinez-Agosto, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 15, 2010
Identification of candidate tumor oncogenes by integrative molecular analysis of choroidal melanoma fine-needle aspiration biopsy specimensTara A McCannel, Barry L Burgess, Nagesh P Rao, et al.
Nucleic Acids Research|December 16, 2004
Detecting tissue-specific regulation of alternative splicing as a qualitative change in microarray dataKeith Le, Katherine Mitsouras, Meenakshi Roy, et al.
Human Mutation|November 8, 2006
Deletion mapping in Xp21 for patients with complex glycerol kinase deficiency using SNP mapping arraysChristopher M Stanczak, Zugen Chen, Yao-Hua Zhang, et al.
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