Eckhard Korsch

Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain

Renaud Touraine, Tania Attié‐Bitach, E. Manceau et al. · The American Journal of Human Genetics · 2000 · 166 citations · Full text

Neurodegenerative Diseases, Developmental Biology, Mendelian Disorder +10

Four Novel Mutations of the LHX3 Gene Cause Combined Pituitary Hormone Deficiencies with or without Limited Neck Rotation

Roland Pfaeffle, Jesse J. Savage, Chad S. Hunter et al. · The Journal of Clinical Endocrinology & Metabolism · 2007 · 121 citations

A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia

Éva Morava, Renate Zeevaert, Eckhard Korsch et al. · European Journal of Human Genetics · 2007 · 101 citations · Full text

Cog7 Gene, Developmental Biology, Common Mutation +6

Natural rubber latex allergy: prevalence and risk factors in patients with spina bifida compared with atopic children and controls

R. Cremer, A. Hoppe, Eckhard Korsch et al. · European Journal of Pediatrics · 1998 · 78 citations

Asthma, Food Allergy, Allergy +11

<b><i>MKRN3</i></b> Mutations in Familial Central Precocious Puberty

Felix Schreiner, Bettina Gohlke, Michaela Hamm et al. · Hormone Research in Paediatrics · 2014 · 61 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +11