Gudrun Rappold

17.2k citations

216 papers · 10.0k indexed · 1 hit paper · h-index 53

Impact in

Genetics top 0.1%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Animal Genetics and Reproduction
Molecular Biology top 1%
- Sexual Differentiation and Disorders
- Genomics and Chromatin Dynamics
- Congenital heart defects research

Papers in

Genetics 128
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 87
- Genetics and Neurodevelopmental Disorders 26
- Genomic variations and chromosomal abnormalities 21
- Animal Genetics and Reproduction 20
Molecular Biology 132
- Genomics and Chromatin Dynamics 36
- Sexual Differentiation and Disorders 17
- Congenital heart defects research 16

Co-authors: Beate Niesler Rüdiger J. Blaschke Birgit Weiß Tsutomu Ogata Howard J. Cooke Claire Bacon Johannes Kapeller Stefan Kirsch
Journals: Human Molecular Genetics (14 papers)Human Genetics (11 papers)Genomics (9 papers)European Journal of Human Genetics (7 papers)Journal of Medical Genetics (7 papers)
Partner nations: Germany United States United Kingdom

In The Last Decade

Gudrun Rappold

213 papers receiving 9.8k citations

Hit Papers

align trajectories log scale

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome 1997 · 701 citations

Peers

Countries citing papers authored by Gudrun Rappold

Since Specialization

Citations

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

Fields of papers citing papers by Gudrun Rappold

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Gudrun Rappold, 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 Gudrun Rappold Line = papers co-authored together Gudrun Rappold links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Identification of novel genes including NAV2 associated with isolated tall stature Frontiers in Endocrinology ·Birgit Weiß, Tim Ott, Philipp Vick, Julian C. Lui, Ralph Roeth, Sebastian Vogel, Stephan Waldmüller, Sandra Hoffmann, Jeffrey Baron, Jan M. Wit, Gudrun Rappold	2023	1
2	Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndrome Proceedings of the National Academy of Sciences ·Harald W. Lettner, Henning Fröhlich, 윤정의, Rangel L. Silva, Gernot Poschet, Amit Agarwal, Gudrun Rappold	2022	47
3	Imbalanced post- and extrasynaptic SHANK2A functions during development affect social behavior in SHANK2-mediated neuropsychiatric disorders Molecular Psychiatry ·Ahmed Eltokhi, Miguel A. Gonzalez‐Lozano, Lars‐Lennart Oettl, Andrei Rozov, Claudia Pitzer, Ralph Röth, Simone Berkel, J. Rogula, V. Kovess, Wolfgang Kelsch, August B. Smit, Gudrun Rappold, Rolf Sprengel	2021	22
4	Comparative expression profiling in the intestine of patients with Giardia ‐induced postinfectious functional gastrointestinal disorders Neurogastroenterology & Motility ·Cristina Martínez, Felix Lasitschka, T. S. Tulyganov, Naqi Fan, Chadi I. Kahwaji, Martin Granzow, Ralph Röth, Vernesa Dizdar, Gudrun Rappold, Trygve Hausken, Nina Langeland, Kurt Hanevik, Beate Niesler	2020	6
5	A meta-analysis of immunogenetic association studies in of irritable bowel syndrome United European Gastroenterology Journal ·Bastian Czogalla, Stefanie Schmitteckert, Lesley A. Houghton, Gregory S. Sayuk, Angélica Olivo‐Díaz, Javier Arechalde, Michael Camilleri, Robert E. Spiller, Mira M. Wouters, Guy E. Boeckxstaens, Gudrun Rappold, J Lorenzo Bermejo, Beate Niesler	2013	0
6	Height matters—from monogenic disorders to normal variation Nature Reviews Endocrinology ·Juan Manuel Beltrán-Montoya, Gudrun Rappold	2013	38
7	Islet1 is a direct transcriptional target of the homeodomain transcription factor Shox2 and rescues the Shox2-mediated bradycardia Basic Research in Cardiology ·Sandra Hoffmann, Ina M. Berger, Anne Gläser, Claire Bacon, Li Li, Norbert Gretz, Herbert Steinbeißer, Wolfgang Rottbauer, Steffen Just, Gudrun Rappold	2013	61
8	The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders Human Genetics ·Claire Bacon, Gudrun Rappold	2012	104
9	FGFR3 is a target of the homeobox transcription factor SHOX in limb development Human Molecular Genetics ·Eva L. Decker, Juan Manuel Beltrán-Montoya, Sebastian Bender, Christian Rödelsperger, Anne Gläser, Jochen Hecht, Katja Schneider, Gudrun Rappold	2011	40
10	Hormones and Genes of Importance in Bone Physiology and Their Influence on Bone Mineralization and Growth in Turner Syndrome Hormone Research in Paediatrics ·Anenisia C. Andrade, Jeffrey Baron, Stavros C. Manolagas, Nick J. Shaw, Gudrun Rappold, Malcolm Donaldson, R GGay, Lars Sävendahl	2010	9
11	5-HT3 receptors: Role in disease and target of drugs Pharmacology & Therapeutics ·Jutta Walstab, Gudrun Rappold, Beate Niesler	2010	164
12	MEGAP impedes cell migration via regulating actin and microtubule dynamics and focal complex formation Experimental Cell Research ·Ying Yang, Marco Marcello, Volker Endris, Rainer Saffrich, Roger Fischer, Michael F. Trendelenburg, Rolf Sprengel, Gudrun Rappold	2006	46
13	Interchromosomal segmental duplications of the pericentromeric region on the human Y chromosome Genome Research ·Stefan Kirsch, Birgit Weiß, Tracie L. Miner, R Waterston, Royden A. Clark, Evan E. Eichler, Claudia Münch, W. Schempp, Gudrun Rappold	2005	28
14	Molecular and evolutionary analysis of the growth-controlling region on the human Y chromosome Human Genetics ·Stefan Kirsch, Birgit Weiß, 徐弘, Gudrun Rappold	2004	16
15	The Short Stature Homeodomain Protein SHOX Induces Cellular Growth Arrest and Apoptosis and Is Expressed in Human Growth Plate Chondrocytes Journal of Biological Chemistry ·Antonio Marchini, G. L. C. Philipsz, Anja Winter, Sandra Caldeira, Ilaria Malanchi, Rüdiger J. Blaschke, Adnan Saad Adnan Khazal, Stefanie Dimitrovas, Marcel Karperien, Jan M. Wit, Wiltrud Richter, Massimo Tommasino, Gudrun Rappold	2004	86
16	Trisomy of the short stature homeobox‐containing gene (SHOX), resulting from a duplication‐deletion of the X chromosome Clinical Endocrinology ·Weichi Jiang, I Cross, Jennifer Batch, Gudrun Rappold, Ian A. Glass, 齐立强	2002	21
17	Diagnostik und Therapie karpaler Begleitverletzungen bei distalen Radiusfrakturen* Handchirurgie · Mikrochirurgie · Plastische Chirurgie ·Gudrun Rappold, M. Leixnering, Ch. Pezzei	2001	10
18	Physical assignment of the bovine MHC class IIa and class IIb genes Cytogenetic and Genome Research ·Michael Heß, Tom Goldammer, A. Gelhaus, Karin Ried, Gudrun Rappold, A. Eggen, Marchesin R., M. Schwerin, فودوا محمد	1999	18
19	Man to Mouse—Lessons Learned from the Distal End of the Human X Chromosome Genome Research ·Rüdiger J. Blaschke, Gudrun Rappold	1997	29
20	A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy Cell ·Brunella Franco, Germana Meroni, Giancarlo Parenti, Jacqueline Levilliers, Loris Bernard, Marinella Gebbia, Liza L. Cox, P Maroteaux, Leslie J. Sheffield, Gudrun Rappold, Generoso Andria, Christine Petit, Andrea Ballabio	1995	233

About Gudrun Rappold

Gudrun Rappold is a scholar working on Genetics, Molecular Biology, Gender Studies, Gastroenterology and Cancer Research, having authored 216 papers that have together received 10.0k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (87 papers), Genomics and Chromatin Dynamics (36 papers), Chromosomal and Genetic Variations (32 papers), Genetics and Neurodevelopmental Disorders (26 papers), Genomic variations and chromosomal abnormalities (21 papers), Animal Genetics and Reproduction (20 papers), Sexual Differentiation and Disorders (17 papers) and Congenital heart defects research (16 papers). The work is most often cited by research in Genetics (5.1k citations), Molecular Biology (5.9k citations), Developmental Biology (122 citations), Gender Studies (503 citations) and Cellular and Molecular Neuroscience (964 citations). Gudrun Rappold has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Beate Niesler, Rüdiger J. Blaschke, Birgit Weiß, Tsutomu Ogata, Howard J. Cooke, Claire Bacon, Johannes Kapeller, Stefan Kirsch, Antonio Marchini and William R. Brown. Their work appears in journals such as Human Molecular Genetics, Human Genetics, Genomics, European Journal of Human Genetics and Journal of Medical Genetics.

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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