Georg Leipold

A Novel 22q11.2 Microdeletion in DiGeorge Syndrome

Anita Rauch, Rudolf A. Pfeiffer, Georg Leipold et al. · The American Journal of Human Genetics · 1999 · 105 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

Incidence and significance of 22q11.2 hemizygosity in patients with interrupted aortic arch

Anita Rauch, Michael Hofbeck, Georg Leipold et al. · American Journal of Medical Genetics · 1998 · 73 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Azathioprine‐induced severe pancytopenia due to a homozygous two‐point mutation of the thiopurine methyltransferase gene in a patient with juvenile HLA‐B27‐associated spondylarthritis

Georg Leipold, Ekkehard Schütz, Johannes‐Peter Haas et al. · Arthritis & Rheumatism · 1997 · 73 citations

Life Sciences, Genetics, Hematology +17

Serum neurofilament light chain reference database for individual application in paediatric care: a retrospective modelling and validation study

Ahmed Abdelhak, Franziska Petermeier, Pascal Benkert et al. · The Lancet Neurology · 2023 · 53 citations · Full text

Medicine, Neurology, Pediatrics +5

Monosomy 22q11 in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries

Michael Hofbeck, Anita Rauch, G. Buheitel et al. · Heart · 1998 · 49 citations · Full text

Medicine, Cardiology, Pediatrics +15