Detailed phenotype–genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader–Willi-like phenotype

Profound obesity associated with a balanced translocation that disrupts the SIM1 gene

J. L. · Human Molecular Genetics · 2000 · 396 citations · Full text

Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome

Eva Klopocki, Harald Schulze, Gabriele Strauß et al. · The American Journal of Human Genetics · 2007 · 367 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +7

Linkage and association of the glutamate receptor 6 gene with autism

Stéphane Jamain, Catalina Betancur, Hélène Quach et al. · Molecular Psychiatry · 2002 · 304 citations · Full text

Glutamate Receptor 6, Syndromic Autism, Genetics +7

Identification and characterization of a second melanin-concentrating hormone receptor, MCH-2R

Andreas W. Sailer, Hideki Sano, Zhizhen Zeng et al. · Proceedings of the National Academy of Sciences · 2001 · 239 citations · Full text

The Three-Factor Eating Questionnaire, body mass index, and responses to sweet and salty fatty foods: a twin study of genetic and environmental associations

Kaisu Keskitalo, Hely Tuorila, Tim D. Spector et al. · American Journal of Clinical Nutrition · 2008 · 218 citations

Food Choice, Obesity, Nutrition +8