Published in Am J Med Genet A on August 17, 2012
Growth charts for non-growth hormone treated Prader-Willi syndrome. Pediatrics (2014) 0.78
Nutritional phases in Prader-Willi syndrome. Am J Med Genet A (2011) 2.08
Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology. Expert Rev Mol Med (2005) 2.04
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay. Hum Genet (2011) 1.94
Neural mechanisms associated with food motivation in obese and healthy weight adults. Obesity (Silver Spring) (2009) 1.88
Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome. Pediatrics (2006) 1.36
Neural mechanisms underlying hyperphagia in Prader-Willi syndrome. Obesity (Silver Spring) (2006) 1.30
X chromosome gene expression in human tissues: male and female comparisons. Genomics (2006) 1.26
Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism. Autism Res (2008) 1.21
Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patients. Am J Med Genet A (2007) 1.16
Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism? J Autism Dev Disord (2004) 1.14
ANKRD11 gene deletion in a 17-year-old male. Clin Dysmorphol (2011) 1.09
Gene expression in cardiac tissues from infants with idiopathic conotruncal defects. BMC Med Genomics (2011) 1.07
snoTARGET shows that human orphan snoRNA targets locate close to alternative splice junctions. Gene (2007) 1.07
Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities. Genet Test (2007) 1.07
Gastric rupture and necrosis in Prader-Willi syndrome. J Pediatr Gastroenterol Nutr (2007) 1.06
Whole genome microarray analysis of gene expression in Prader-Willi syndrome. Am J Med Genet A (2007) 1.06
Maladaptive behaviors and risk factors among the genetic subtypes of Prader-Willi syndrome. Am J Med Genet A (2005) 1.04
Whole genome microarray analysis of gene expression in subjects with fragile X syndrome. Genet Med (2007) 1.04
A 9-year-old male with a duplication of chromosome 3p25.3p26.2: clinical report and gene expression analysis. Am J Med Genet A (2006) 1.03
Newborn with anophthalmia and features of Fryns syndrome. Pediatr Dev Pathol (2002) 1.00
Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafness. Arch Otolaryngol Head Neck Surg (2005) 0.98
Body composition and fatness patterns in Prader-Willi syndrome: comparison with simple obesity. Obesity (Silver Spring) (2006) 0.96
Mass Screening for Severe Problem Behavior among Infants and Toddlers In Peru. J Ment Health Res Intellect Disabil (2012) 0.96
Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for years. Arch Pathol Lab Med (2006) 0.95
A clinical report and further delineation of the 14q32 deletion syndrome. Clin Dysmorphol (2011) 0.95
Risk factors for self-injury, aggression, and stereotyped behavior among young children at risk for intellectual and developmental disabilities. Am J Intellect Dev Disabil (2014) 0.94
Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD. Genomics (2005) 0.93
Metabolic syndrome in South Asian immigrants: more than low HDL requiring aggressive management. Lipids Health Dis (2011) 0.90
Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome. Am J Med Genet A (2007) 0.89
Genetics and mitochondrial abnormalities in autism spectrum disorders: a review. Curr Genomics (2011) 0.89
IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features. Eur J Med Genet (2011) 0.85
Deaths due to choking in Prader-Willi syndrome. Am J Med Genet A (2007) 0.84
The neuroanatomy of genetic subtype differences in Prader-Willi syndrome. Am J Med Genet B Neuropsychiatr Genet (2012) 0.84
A clinical case report and literature review of the 3q29 microdeletion syndrome. Clin Dysmorphol (2015) 0.83
An 18-year follow-up report on an infant with a duplication of 9q34. Am J Med Genet A (2010) 0.83
Ghrelin, peptide YY and their receptors: gene expression in brain from subjects with and without Prader-Willi syndrome. Int J Mol Med (2005) 0.82
Triaging patients at risk of influenza using a patient portal. J Am Med Inform Assoc (2011) 0.81
Double-blind, randomized placebo-controlled clinical trial of benfotiamine for severe alcohol dependence. Drug Alcohol Depend (2013) 0.81
Drowning as a cause of death in Angelman syndrome. Am J Ment Retard (2002) 0.81
Eye abnormalities in Fryns syndrome. Am J Med Genet A (2004) 0.80
Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome. Genet Test Mol Biomarkers (2011) 0.80
X chromosome inactivation in women with alcoholism. Alcohol Clin Exp Res (2012) 0.80
Hyperphagia: current concepts and future directions proceedings of the 2nd international conference on hyperphagia. Obesity (Silver Spring) (2014) 0.80
TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome. J Child Psychol Psychiatry (2011) 0.80
Loxapine add-on for adolescents and adults with autism spectrum disorders and irritability. J Child Adolesc Psychopharmacol (2015) 0.79
Apo lipoprotein A1 gene polymorphisms predict cardio-metabolic risk in South Asian immigrants. Dis Markers (2012) 0.79
APOA1 gene polymorphisms in the South Asian immigrant population in the United States. Indian J Hum Genet (2011) 0.79
12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes. Clin Dysmorphol (2012) 0.79
Expanding the phenotype of SPONASTRIME dysplasia to include short dental roots, hypogammaglobulinemia, and cataracts. Am J Med Genet A (2008) 0.79
Clonality studies in sacral chordoma. Cancer Genet Cytogenet (2006) 0.79
Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome. J Clin Invest (2016) 0.79
Comparison of biological specimens and DNA collection methods for PCR amplification and microarray analysis. Clin Chem Lab Med (2013) 0.79
Oculoauriculofrontonasal syndrome (OAFNS) in a nine-month-old male. Am J Med Genet (2002) 0.79
Exon microarray analysis of human dorsolateral prefrontal cortex in alcoholism. Alcohol Clin Exp Res (2014) 0.78
Follicle stimulating and leutinizing hormones, estradiol and testosterone in Prader-Willi syndrome. Am J Med Genet A (2008) 0.78
Autistic and dysmorphic features associated with a submicroscopic 2q33.3-q34 interstitial deletion detected by array comparative genomic hybridization. Am J Med Genet A (2008) 0.77
Genomics of childhood obesity. Curr Genomics (2011) 0.77
Deletion of TOP3B Is Associated with Cognitive Impairment and Facial Dysmorphism. Cytogenet Genome Res (2016) 0.76
TPH2 polymorphisms and expression in Prader-Willi syndrome subjects with differing genetic subtypes. J Neurodev Disord (2010) 0.76
Laparoscopic sleeve gastrectomy in 108 obese children and adolescents ages 5 to 21 years by Alqahtani AR, Antonisamy B, Alamri H, Elahmedi M, Zimmerman VA. Ann Surg (2015) 0.75
14q32 deletion syndrome: a clinical report. Clin Dysmorphol (2012) 0.75
Marshall-Smith syndrome: Follow-up report of a four and a half year old male. Am J Med Genet A (2004) 0.75
45,X/46,XY mosaicism and fragile X syndrome. Am J Med Genet A (2003) 0.75
Letter to the editor: Long-term experience with duodenal switch in adolescents. Obes Surg (2012) 0.75
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. J Med Genet (2012) 0.75
GENETIC AND OTHER HEALTH PROBLEMS ASCERTAINED IN FAMILIES OF THE DAUGHTERS OF THE AMERICAN REVOLUTION. Dysmorphol Clin Genet (1991) 0.75
Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(15;19)(q12;p13.3). Cytogenet Genome Res (2016) 0.75
Distal Partial Trisomy 15q26 and Partial Monosomy 16p13.3 in a 36-Year-Old Male with Clinical Features of Both Chromosomal Abnormalities. Cytogenet Genome Res (2015) 0.75
Progress in pediatric cardiology ("Genetics of Pediatric Heart Disease"). Prog Pediatr Cardiol (2005) 0.75