Karin Segers

Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>

Yanick J. Crow, Diana Chase, Johanna L. Schmidt et al. · American Journal of Medical Genetics Part A · 2015 · 589 citations · Full text

Human–Ovine Comparative Sequencing of a 250-kb Imprinted Domain Encompassing the Callipyge (<i>clpg</i>) Locus and Identification of Six Imprinted Transcripts: <i>DLK1</i>, <i>DAT, GTL2, PEG11, antiPEG11</i>, and <i>MEG8</i>

Carole Charlier, Karin Segers, Danny Wagenaar et al. · Genome Research · 2001 · 208 citations · Full text

Genetics, Genomic Mechanism, Gene Characterization +19

The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting status

Carole Charlier, Karin Segers, Latifa Karim et al. · Nature Genetics · 2001 · 170 citations

Transcriptional Regulation, Genetic Disorder, Natural Sciences +11

Comparative Sequence Analysis of the Imprinted <i>Dlk1–Gtl2</i> Locus in Three Mammalian Species Reveals Highly Conserved Genomic Elements and Refines Comparison with the <i>Igf2–H19</i> Region

Martina Paulsen, Shuji Takada, Neil A. Youngson et al. · Genome Research · 2001 · 124 citations · Full text

Mosaicism of Solid Gold Supports the Causality of a Noncoding A-to-G Transition in the Determinism of the Callipyge Phenotype

Maria A. Smit, Karin Segers, Laura G. Carrascosa et al. · Genetics · 2003 · 107 citations