Christina Lich
University of Duisburg-Essen(DE)
Publications by Year
Research Areas
Genetic Syndromes and Imprinting, Epigenetics and DNA Methylation, Genomic variations and chromosomal abnormalities, Prenatal Screening and Diagnostics, Cleft Lip and Palate Research
Most-Cited Works
- → Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect(2003)367 cited
- → Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis(1998)216 cited
- → Maternal methylation imprints on human chromosome 15 are established during or after fertilization(2001)200 cited
- A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locus.(1997)
- → A Single-Tube PCR Test for the Diagnosis of Angelman and Prader-Willi Syndrome Based on Allelic Methylation Differences at the SNRPN Locus(1997)147 cited
- → A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp(1999)96 cited
- → Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome.(1996)82 cited
- → A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defect(1999)79 cited
- → Clinical features of maternal uniparental disomy 14 in patients with an epimutation and a deletion of the imprintedDLK1/GTL2gene cluster(2008)71 cited
- → Disruption of the Bipartite Imprinting Center in a Family with Angelman Syndrome(2001)67 cited