Christina Lich

1.7k total citations
16 papers, 1.0k citations indexed

About

Christina Lich is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Christina Lich has authored 16 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 11 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Christina Lich's work include Genetic Syndromes and Imprinting (14 papers), Epigenetics and DNA Methylation (11 papers) and Genomic variations and chromosomal abnormalities (8 papers). Christina Lich is often cited by papers focused on Genetic Syndromes and Imprinting (14 papers), Epigenetics and DNA Methylation (11 papers) and Genomic variations and chromosomal abnormalities (8 papers). Christina Lich collaborates with scholars based in Germany, Austria and United Kingdom. Christina Lich's co-authors include Karin Buiting, Bernhard Horsthemke, Michael Zeschnigk, Walter Doerfler, Osman El‐Maarri, Gabriele Gillessen‐Kaesbach, Stephanie Groß, Angela Barnicoat, Klaus Wagner and S Cottrell and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

Christina Lich

16 papers receiving 975 citations

Peers

Christina Lich

GENET

PPCH

PHEOH

PFM

J. Edward Spence United States

Anne Le Digarcher France

Roel Hordijk Netherlands

M. S. NEWTON United Kingdom

Laëtitia Chotard Canada

Christel Thauvin‐Robinet France

Kathrin S. Precht United States

Tracy Brandt United States

N. Créau-Goldberg France

Jasmin Beygo Germany

J. Edward Spence United States

Christina Lich

615 ×0.7

GENET

527 ×0.7

361 ×0.8

PPCH

26 ×0.7

PHEOH

26 ×0.8

PFM

Citations per year, relative to Christina Lich Christina Lich (= 1×) peers J. Edward Spence

Countries citing papers authored by Christina Lich

Since Specialization

Citations

This map shows the geographic impact of Christina Lich's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Christina Lich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christina Lich more than expected).

Fields of papers citing papers by Christina Lich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christina Lich. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Christina Lich. The network helps show where Christina Lich may publish in the future.

Co-authorship network of co-authors of Christina Lich

This figure shows the co-authorship network connecting the top 25 collaborators of Christina Lich. A scholar is included among the top collaborators of Christina Lich based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Christina Lich. Christina Lich is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

Beygo, Jasmin, Karin Buiting, Saskia Seland, et al.. (2011). First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome. Molecular Syndromology. 2(2). 53–59. 16 indexed citations

Horsthemke, Bernhard, Christina Lich, Birgitta Sauer, et al.. (2010). Parental origin and functional relevance of a de novo UBE3A variant. European Journal of Medical Genetics. 54(1). 19–24. 7 indexed citations

Buiting, Karin, Deniz Kanber, José I. Martı́n-Subero, et al.. (2008). Clinical features of maternal uniparental disomy 14 in patients with an epimutation and a deletion of the imprintedDLK1/GTL2gene cluster. Human Mutation. 29(9). 1141–1146. 57 indexed citations

Buiting, Karin, Stephanie Groß, Christina Lich, et al.. (2003). Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect. The American Journal of Human Genetics. 72(3). 571–577. 208 indexed citations

Zeschnigk, Michael, et al.. (2003). Methylation analysis of several tumour suppressor genes shows a low frequency of methylation of CDKN2A and RARB in uveal melanomas. Comparative and Functional Genomics. 4(3). 329–336. 18 indexed citations

El‐Maarri, Osman, Karin Buiting, Peter M. Kroisel, et al.. (2001). Maternal methylation imprints on human chromosome 15 are established during or after fertilization. Nature Genetics. 27(3). 341–344. 159 indexed citations

Buiting, Karin, Angela Barnicoat, Christina Lich, et al.. (2001). Disruption of the Bipartite Imprinting Center in a Family with Angelman Syndrome. The American Journal of Human Genetics. 68(5). 1290–1294. 50 indexed citations

Runte, Maren, Christina Lich, Michael Zeschnigk, et al.. (2001). Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15. European Journal of Human Genetics. 9(7). 519–526. 9 indexed citations

Buiting, Karin, Peter M. Kroisel, Klaus Wagner, et al.. (2000). Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselling. Clinical Genetics. 58(4). 284–290. 20 indexed citations

10.

Buiting, Karin, Bärbel Dittrich, Bernd Dworniczak, et al.. (1999). A 28-kb Deletion Spanning D15S63 (PW71) in Five Families: A Rare Neutral Variant?. The American Journal of Human Genetics. 65(6). 1588–1594. 7 indexed citations

11.

Gillessen‐Kaesbach, Gabriele, Stephanie Demuth, Hannelore Thiele, et al.. (1999). A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defect. European Journal of Human Genetics. 7(6). 638–644. 62 indexed citations

12.

Buiting, Karin, Christina Lich, S Cottrell, Angela Barnicoat, & Bernhard Horsthemke. (1999). A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp. Human Genetics. 105(6). 665–666. 79 indexed citations

13.

Bürger, Joachim, Bärbel Dittrich, Christina Lich, et al.. (1997). Different Mechanisms and Recurrence Risks of Imprinting Defects in Angelman Syndrome. The American Journal of Human Genetics. 61(1). 88–93. 44 indexed citations

14.

Zeschnigk, Michael, Christina Lich, Karin Buiting, Walter Doerfler, & Bernhard Horsthemke. (1997). A Single-Tube PCR Test for the Diagnosis of Angelman and Prader-Willi Syndrome Based on Allelic Methylation Differences at the SNRPN Locus. European Journal of Human Genetics. 5(2). 94–98. 122 indexed citations

15.

Zeschnigk, Michael, et al.. (1997). A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locus.. PubMed. 5(2). 94–8. 135 indexed citations

16.

Horsthemke, Bernhard, Anneke Maat‐Kievit, A. van den Ouweland, et al.. (1996). Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome.. Journal of Medical Genetics. 33(10). 848–851. 28 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact