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Markus Stümm | Researchclopedia

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Markus Stümm

Sana Klinikum Lichtenberg

142

Works

5,457

Citations

32

h-index

59

i10-index

Research Topics

Prenatal Screening and Diagnostics Genomic variations and chromosomal abnormalities DNA Repair Mechanisms

Affiliations

Arkansas Children's Hospital2003–2003

Harvard University2003–2003

Max Planck Society2001–2001

Universität Hamburg1998–1998

University of Sussex2003–2003

Top Works

Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome

Raymonda Varon,Christine Vissinga,et al.

19981,077 citations

Chromosomal and Genetic Variations

Carcinogens and Genotoxicity Assessment

DNA Ligase IV Mutations Identified in Patients Exhibiting Developmental Delay and Immunodeficiency

Mark O’Driscoll,Karen Cerosaletti,et al.

2001537 citations

Bassoon, a Novel Zinc-finger CAG/Glutamine-repeat Protein Selectively Localized at the Active Zone of Presynaptic Nerve Terminals

Susannetom Dieck,Lydia Sanmartı́-Vila,et al.

1998482 citations

Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChlR1

Petra van der Lelij,Krystyńa Chrzańowska,et al.

2010271 citations

Human RAD50 Deficiency in a Nijmegen Breakage Syndrome-like Disorder

Regina Waltes,Reinhard Kalb,et al.

2009258 citations

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements

Heike Starke,Jörg Seidel,et al.

2002204 citations

Nonhomologous end joining and V(D)J recombination require an additional factor

Yan Dai,Boris Kysela,et al.

2003187 citations

Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification

Heike Starke,Angela Nietzel,et al.

2003162 citations

Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticum

Berthold Struk,Li Cai,et al.

2000144 citations