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Matthias Begemann

Showing results (11-20 of 97) with videos related to

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American Journal of Medical Genetics. Part A|October 9, 2015
No major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disordersAnne Müller, Lukas Soellner, Gerhard Binder, et al.
Expert Review of Molecular Diagnostics|June 19, 2012
Epigenetic and genetic diagnosis of Silver-Russell syndromeThomas Eggermann, Sabrina Spengler, Magdalena Gogiel, et al.
NAR Genomics and Bioinformatics|July 25, 2025
Utilizing protein structure graph embeddings to predict the pathogenicity of missense variantsMartin Danner, Matthias Begemann, Miriam Elbracht, et al.
Human Reproduction Update|February 19, 2020
Disturbed genomic imprinting and its relevance for human reproduction: causes and clinical consequencesMiriam Elbracht, Deborah Mackay, Matthias Begemann, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|March 3, 2025
Vasculopathy with neurological symptomsMorna F Schmidt, Jan van der Laden, Matthias Begemann, et al.
Clinical Epigenetics|February 17, 2019
Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulationFlorian Kraft, Katharina Wesseler, Matthias Begemann, et al.
Epigenetics|March 16, 2012
Use of multilocus methylation-specific single nucleotide primer extension (MS-SNuPE) technology in diagnostic testing for human imprinted lociMatthias Begemann, Isabelle Leisten, Lukas Soellner, et al.
BMC Genomics|March 15, 2025
Mutational constraint analysis workflow for overlapping short open reading frames and genomic neighborsMartin Danner, Matthias Begemann, Florian Kraft, et al.
Molecular Genetics & Genomic Medicine|August 13, 2018
Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patientsThomas Eggermann, Susanne Ledig, Matthias Begemann, et al.
European Journal of Medical Genetics|December 23, 2015
First report on concordant monozygotic twins with Silver-Russell syndrome and ICR1 hypomethylationAngelika Riess, Gerhard Binder, Julian Ziegler, et al.
Pageof 10

Showing results (11-20 of 97) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics. Part A|October 9, 2015
No major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disordersAnne Müller, Lukas Soellner, Gerhard Binder, et al.
Expert Review of Molecular Diagnostics|June 19, 2012
Epigenetic and genetic diagnosis of Silver-Russell syndromeThomas Eggermann, Sabrina Spengler, Magdalena Gogiel, et al.
NAR Genomics and Bioinformatics|July 25, 2025
Utilizing protein structure graph embeddings to predict the pathogenicity of missense variantsMartin Danner, Matthias Begemann, Miriam Elbracht, et al.
Human Reproduction Update|February 19, 2020
Disturbed genomic imprinting and its relevance for human reproduction: causes and clinical consequencesMiriam Elbracht, Deborah Mackay, Matthias Begemann, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|March 3, 2025
Vasculopathy with neurological symptomsMorna F Schmidt, Jan van der Laden, Matthias Begemann, et al.
Clinical Epigenetics|February 17, 2019
Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulationFlorian Kraft, Katharina Wesseler, Matthias Begemann, et al.
Epigenetics|March 16, 2012
Use of multilocus methylation-specific single nucleotide primer extension (MS-SNuPE) technology in diagnostic testing for human imprinted lociMatthias Begemann, Isabelle Leisten, Lukas Soellner, et al.
BMC Genomics|March 15, 2025
Mutational constraint analysis workflow for overlapping short open reading frames and genomic neighborsMartin Danner, Matthias Begemann, Florian Kraft, et al.
Molecular Genetics & Genomic Medicine|August 13, 2018
Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patientsThomas Eggermann, Susanne Ledig, Matthias Begemann, et al.
European Journal of Medical Genetics|December 23, 2015
First report on concordant monozygotic twins with Silver-Russell syndrome and ICR1 hypomethylationAngelika Riess, Gerhard Binder, Julian Ziegler, et al.
Pageof 10