Peter Wieacker
University of Münster(DE)
Publications by Year
Research Areas
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Sexual Differentiation and Disorders, Genomic variations and chromosomal abnormalities, Sperm and Testicular Function, Prenatal Screening and Diagnostics
Most-Cited Works
- → Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study(2012)1,063 cited
- → X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes(2015)302 cited
- → Mutations of the Ephrin-B1 Gene Cause Craniofrontonasal Syndrome(2004)239 cited
- → WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes(2009)228 cited
- → The mutational spectrum in Waardenburg syndrome(1995)223 cited
- → Pathophysiological Mechanisms of Dominant and Recessive KvLQT1 K+ Channel Mutations Found in Inherited Cardiac Arrhythmias(1997)189 cited
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