Christa Lese‐Martin
Institute of Human Genetics(PL)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Autism Spectrum Disorder Research, Prenatal Screening and Diagnostics, Epigenetics and DNA Methylation, Chromosomal and Genetic Variations
Most-Cited Works
- → Strong Association of De Novo Copy Number Mutations with Autism(2007)2,825 cited
- → Mapping autism risk loci using genetic linkage and chromosomal rearrangements(2007)1,388 cited
- → 15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q(2009)128 cited
- → Quantitative Proteomic and Genetic Analyses of the Schizophrenia Susceptibility Factor Dysbindin Identify Novel Roles of the Biogenesis of Lysosome-Related Organelles Complex 1(2012)86 cited
- → Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3‐pter(2005)75 cited