Birgit Weiß
Heidelberg University(DE)
Publications by Year
Research Areas
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Genomics and Chromatin Dynamics, Thyroid Disorders and Treatments, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome(1997)947 cited
- → Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation(2010)575 cited
- → A human pseudoautosomal gene, ADP/ATP translocase, escapes X–inactivation whereas a homologue on Xq is subject to X–inactivation(1993)76 cited
- → Expression of Apolipoprotein A‐I in Porcine Brain Endothelium In Vitro(1994)75 cited
- → BNP is a transcriptional target of the short stature homeobox gene SHOX(2007)69 cited
- → Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patients.(2001)62 cited
- → Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation(2016)50 cited
- → Biodiversity, the ultimate agri-environmental indicator?(2003)49 cited
- → Investigation of SHANK3 in schizophrenia(2017)41 cited
- → Interchromosomal segmental duplications of the pericentromeric region on the human Y chromosome(2005)37 cited