Karin Buiting

10.8k citations

121 papers · 6.6k indexed · h-index 43

Impact in

Genetics top 0.1%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Pediatrics, Perinatology and Child Health top 0.2%
- Prenatal Screening and Diagnostics

Papers in ⓘ

Genetics 114
- Genetic Syndromes and Imprinting 111
- Genomic variations and chromosomal abnormalities 27
- Genetics and Neurodevelopmental Disorders 6
Pediatrics, Perinatology and Child Health 61
- Prenatal Screening and Diagnostics 61

Co-authors: Bernhard Horsthemke (69 shared papers)Bärbel Dittrich (12 shared papers)Stephanie Groß (8 shared papers)Christina Lich (12 shared papers)Robert D. Nicholls (9 shared papers)Charles A. Williams (6 shared papers)Shinji Saitoh (7 shared papers)Gabriele Gillessen‐Kaesbach (19 shared papers)
Journals: European Journal of Human Genetics (19 papers)Human Molecular Genetics (11 papers)The American Journal of Human Genetics (7 papers)Genomics (6 papers)Cytogenetic and Genome Research (6 papers)
Partner nations: Germany United States United Kingdom

In The Last Decade

Karin Buiting

121 papers receiving 6.3k citations

Peers

Countries citing papers authored by Karin Buiting

Since Specialization

Citations

This map shows the geographic impact of Karin Buiting'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 Karin Buiting with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karin Buiting more than expected).

Fields of papers citing papers by Karin Buiting

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karin Buiting. 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 Karin Buiting. The network helps show where Karin Buiting may publish in the future.

Co-authors

The 25 scholars most cited alongside Karin Buiting, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Karin Buiting Line = papers co-authored together Karin Buiting links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 121 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15 Nature Genetics ·Karin Buiting, Shinji Saitoh, Stephanie Groß, Bärbel Dittrich, Stuart Schwartz, Robert D. Nicholls, Bernhard Horsthemke	1995	471
2	Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization Proceedings of the National Academy of Sciences ·Jérôme Cavaillé, Karin Buiting, Martin Kiefmann, Marc Lalande, Camilynn I. Brannan, Bernhard Horsthemke, Jean‐Pierre Bachellerie, Jürgen Brosius, Alexander Hüttenhofer	2000	466
3	Angelman syndrome — insights into a rare neurogenetic disorder Nature Reviews Neurology ·Karin Buiting, Charles A. Williams, Bernhard Horsthemke	2016	242
4	Prader–Willi syndrome and Angelman syndrome American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Karin Buiting	2010	221
5	Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect The American Journal of Human Genetics ·Karin Buiting, Stephanie Groß, Christina Lich, Gabriele Gillessen‐Kaesbach, Osman El‐Maarri, Bernhard Horsthemke	2003	208
6	Genomic Organization and Partial Duplication of the Human α7 Neuronal Nicotinic Acetylcholine Receptor Gene (CHRNA7) Genomics ·Judith Gault, Misi Robinson, Ralph Berger, Carla Drebing, Judith Logel, Jan Hopkins, T. C. Moore, Suzette Jacobs, Jennifer Meriwether, Mun Jun Choi, Eun Jung Kim, K. Walton, Karin Buiting, A DAVIS, Charles R. Breese, Robert Freedman, Sherry Leonard	1998	207
7	Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene Nature Genetics ·Bärbel Dittrich, Karin Buiting, Bernd Korn, Sarah Rickard, Jessica L. Buxton, Shinji Saitoh, Robert D. Nicholls, Poustka Annemarie, Andreas Winterpacht, Bernhard Zabel, Bernhard Horsthemke	1996	197
8	Imprinting-Mutation Mechanisms in Prader-Willi Syndrome The American Journal of Human Genetics ·Tohru Ohta, Todd A. Gray, Peter K. Rogan, Karin Buiting, James M. Gabriel, Shinji Saitoh, Bethi Muralidhar, B. Bilienska, Małgorzata Krajewska‐Walasek, Daniel J. Driscoll, Bernhard Horsthemke, Merlin G. Butler, Robert D. Nicholls	1999	195
9	Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes. PubMed ·André Reis, Bärbel Dittrich, Valerie Greger, Karin Buiting, M. Lalande, Gabriele Gillessen‐Kaesbach, Maria Anvret, Bernhard Horsthemke	1994	188
10	Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13 Human Genetics ·B�rbel Dittrich, WendyP. Robinson, Hans Knoblauch, Karin Buiting, Kerstin Schmidt, Gabriele Gillessen‐Kaesbach, Bernhard Horsthemke	1992	171
11	Maternal methylation imprints on human chromosome 15 are established during or after fertilization Nature Genetics ·Osman El‐Maarri, Karin Buiting, Edwin G. Peery, Peter M. Kroisel, Başak Balaban, Klaus Wagner, Bülent Urman, Julia Heyd, Christina Lich, Camilynn I. Brannan, Jörn Walter, Bernhard Horsthemke	2001	159
12	Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations. Proceedings of the National Academy of Sciences ·Shinji Saitoh, Karin Buiting, Peter K. Rogan, Jessica L. Buxton, Daniel J. Driscoll, J Arnemann, Rainer König, S Malcolm, B. Horsthemke, Robert D. Nicholls	1996	146
13	A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locus. PubMed ·Michael Zeschnigk, Christina Lich, Karin Buiting, Walter Doerfler, Bernhard Horsthemke	1997	135
14	De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch Nature Genetics ·Beata Bielińska, Susan M. Blaydes, Karin Buiting, Tao Yang, Małgorzata Krajewska‐Walasek, Bernhard Horsthemke, Camilynn I. Brannan	2000	125
15	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 ·Michael Zeschnigk, Christina Lich, Karin Buiting, Walter Doerfler, Bernhard Horsthemke	1997	122
16	Molecular and Clinical Aspects of Angelman Syndrome Molecular Syndromology ·Aditi I Dagli, Karin Buiting, Charles A. Williams	2011	105
17	Imprinted Segments in the Human Genome: Different Dna Methylation Patterns in the Prader-Willi/Angelman Syndrome Region As Determined by the Genomic Sequencing Method Human Molecular Genetics ·Michael Zeschnigk, Birgit Schmitz, Bärbel Dittrich, Karin Buiting, B. Horsthemke, Walter Doerfler	1997	104
18	A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome European Journal of Human Genetics ·Deniz Kanber, Jacques C. Giltay, Dagmar Wieczorek, Corinna Zogel, Ron Hochstenbach, Almuth Caliebe, Alma Kuechler, Bernhard Horsthemke, Karin Buiting	2008	102
19	Imprinting defects on human chromosome 15 Cytogenetic and Genome Research ·Bernhard Horsthemke, Karin Buiting	2006	94
20	The Human Retinoblastoma Gene Is Imprinted PLoS Genetics ·Deniz Kanber, Tea Berulava, Ole Ammerpohl, Diana Mitter, Julia Richter, Reiner Siebert, Bernhard Horsthemke, Dietmar Lohmann, Karin Buiting	2009	92

About Karin Buiting

Karin Buiting is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Pathology and Forensic Medicine and Genetics, having authored 121 papers that have together received 6.6k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (111 papers), Epigenetics and DNA Methylation (86 papers), Prenatal Screening and Diagnostics (61 papers), Genomic variations and chromosomal abnormalities (27 papers), Genomics and Chromatin Dynamics (8 papers), RNA modifications and cancer (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Tumors and Oncological Cases (5 papers). The work is most often cited by research in Genetics (5.3k citations), Pediatrics, Perinatology and Child Health (2.6k citations), Molecular Biology (5.0k citations), Cancer Research (325 citations) and Pathology and Forensic Medicine (264 citations). Karin Buiting has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Bernhard Horsthemke, Bärbel Dittrich, Stephanie Groß, Christina Lich, Robert D. Nicholls, Charles A. Williams, Shinji Saitoh, Gabriele Gillessen‐Kaesbach, Michael Zeschnigk and Camilynn I. Brannan. Their work appears in journals such as European Journal of Human Genetics, Human Molecular Genetics, The American Journal of Human Genetics, Genomics and Cytogenetic and Genome Research.

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.

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