Sasan Rasi

DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein–Taybi syndrome (RSTS) and in another patient with incomplete RSTS

Oliver Bartsch, Stefanie Schmidt, Marion Richter et al. · Human Genetics · 2005 · 116 citations

Life Sciences, Genetics, Molecular Genetics +7

Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein–Taybi syndrome

Oliver Bartsch, Sasan Rasi, Alicia Delicado et al. · Human Genetics · 2006 · 53 citations

Life Sciences, Genetics, Molecular Genetics +14

Preimplantation genetic diagnosis for chromosome rearrangements – one blastomere biopsy versus two blastomere biopsy

D. Brodie, Claire E. Beyer, Elissa Osborne et al. · Journal of Assisted Reproduction and Genetics · 2012 · 52 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22)

Oliver Bartsch, Sasan Rasi, Kristina Hoffmann et al. · European Journal of Human Genetics · 2005 · 25 citations

Life Sciences, Genetics, Molecular Genetics +16

Hypertrichosis, hyperkeratosis, abnormal corpus callosum, mental retardation and dysmorphic features in three unrelated females

Maarit Peippo, Leena Valanne, K Kuokkanen et al. · Clinical Dysmorphology · 2004 · 19 citations

Medicine, Dermatology, Genetics +16