Your account is not claimed yet. You can sign up with ORCID to claim your account.

Matthias Begemann (M Begemann)

ORCID

Publication Activity (10 Years)

Years Active: 2015-2022
Publications (10 Years): 10

Top Venues

Genes

European journal of human genetics : EJHG

Clinical genetics

Medizinische Fakultät der RWTH Aachen (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Medizinische Fakultät der RWTH Aachen Jul 1o 2009 - Aug 12o 2013

Germany

PHD :: Human Genetics

Publications

K Eggermann, Robert Meyer, Matthias Begemann, D Dey, E Bültmann, I Kurth, G C Korenke, C Knopp
Clonal Elimination of the Pathogenic Allele as Diagnostic Pitfall in SAMD9L -Associated Neuropathy. Genes 13 (12) (2022)
K Eggermann, Robert Meyer, Matthias Begemann, D Dey, E Bültmann, I Kurth, G C Korenke, C Knopp
Clonal Elimination of the Pathogenic Allele as Diagnostic Pitfall in SAMD9L -Associated Neuropathy. Genes 13 (12) (2022)
K Eggermann, Robert Meyer, Matthias Begemann, D Dey, E Bültmann, I Kurth, G C Korenke, C Knopp
Clonal Elimination of the Pathogenic Allele as Diagnostic Pitfall in SAMD9L -Associated Neuropathy. Genes 13 (12) (2022)
K Eggermann, Robert Meyer, Matthias Begemann, D Dey, E Bültmann, I Kurth, G C Korenke, C Knopp
Clonal Elimination of the Pathogenic Allele as Diagnostic Pitfall in SAMD9L -Associated Neuropathy. Genes 13 (12) (2022)
K Eggermann, Robert Meyer, Matthias Begemann, D Dey, E Bültmann, I Kurth, G C Korenke, C Knopp
Clonal Elimination of the Pathogenic Allele as Diagnostic Pitfall in SAMD9L -Associated Neuropathy. Genes 13 (12) (2022)
Natja Haag, Ene Choo Tan, Matthias Begemann, Lars Buschmann, Florian Kraft, Petra Holschbach, Angeline H M Lai, Maggie Brett, Ganeshwaran H Mochida, Stephanie DiTroia, Lynn Pais, Jennifer E Neil, Muna Al-Saffar, Laila Bastaki, Christopher A Walsh, Ingo Kurth, Cordula Knopp
Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability. European journal of human genetics : EJHG 29 (11) (2021)
Eggermann Thomas, Gundula Kadgien, Matthias Begemann, Miriam Elbracht
Biallelic PADI6 variants cause multilocus imprinting disturbances and miscarriages in the same family. European journal of human genetics : EJHG 29 (4) (2020)
Robert Meyer, Matthias Begemann, Stephanie Demuth, Florian Kraft, Daniela Dey, Herdit Schüler, Sabine Busse, Martin G Häusler, Klaus Zerres, Ingo Kurth, Eggermann Thomas, Miriam Elbracht
Inherited cases of CNOT3-associated intellectual developmental disorder with speech delay, autism, and dysmorphic facies. Clinical genetics 98 (4) (2020)
Lukas Soellner, Florian Kraft, Sabrina Sauer, Matthias Begemann, Ingo Kurth, Miriam Elbracht, Thomas Eggermann
Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers. European journal of human genetics : EJHG 27 (1) (2018)
Thomas Eggermann, Frédéric Brioude, Silvia Russo, Maria P Lombardi, Jet Bliek, Eamonn R Maher, Lidia Larizza, Dirk Prawitt, Irène Netchine, Marie Gonzales, Karen Grønskov, Zeynep Tümer, David Monk, Marcel Mannens, Krystyna Chrzanowska, Malgorzata K Walasek, Matthias Begemann, Lukas Soellner, Katja Eggermann, Jair Tenorio, Julián Nevado, Gudrun E Moore, Deborah Jg Mackay, Karen Temple, Gabriele Gillessen-Kaesbach, Tsutomu Ogata, Rosanna Weksberg, Elizabeth Algar, Pablo Lapunzina
Prenatal molecular testing for Beckwith-Wiedemann and Silver-Russell syndromes: a challenge for molecular analysis and genetic counseling. European journal of human genetics : EJHG 24 (6) (2015)

Matthias Begemann.css-eqlu8i{font-size:small;padding-left:4px;} (M Begemann)

Publication Activity (10 Years)

Top Topics

Top Venues

Matthias Begemann (M Begemann)