Hartmut Engels

7.1k citations

66 papers · 2.3k · h-index 26

Impact in

Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Molecular Biology top 10%
- Congenital heart defects research
- Chromatin Remodeling and Cancer

Papers in

Genetics 43
- Genomic variations and chromosomal abnormalities 34
- Genetics and Neurodevelopmental Disorders 17
- Genomics and Rare Diseases 5
- Genetic Syndromes and Imprinting 5
Molecular Biology 28
- Congenital heart defects research 9
- Ion channel regulation and function 5

Co-authors: Gesa Schwanitz (20 shared papers)Dagmar Wieczorek (13 shared papers)Gudrun Rappold (3 shared papers)Ute Moog (4 shared papers)Alexander Hoischen (7 shared papers)Ruthild G. Weber (8 shared papers)Volker Endris (1 shared paper)Eva Wohlleber (8 shared papers)
Journals: Human Genetics (7 papers)European Journal of Human Genetics (7 papers)European Journal of Medical Genetics (3 papers)Human Mutation (3 papers)The American Journal of Human Genetics (2 papers)
Partner nations: Germany Poland United Kingdom

In The Last Decade

Hartmut Engels

64 papers receiving 2.2k citations

Peers

Countries citing papers authored by Hartmut Engels

Since Specialization

Citations

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

Fields of papers citing papers by Hartmut Engels

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Hartmut Engels, 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 Hartmut Engels Line = papers co-authored together Hartmut Engels 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 66 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation Nature Genetics ·Simone Berkel, Christian R. Marshall, Birgit Weiß, Jennifer Howe, Ralph Roeth, Ute Moog, Volker Endris, Wendy Roberts, Péter Szatmári, Dalila Pinto, Michael von Bonin, Angelika Rieß, Hartmut Engels, Rolf Sprengel, Stephen W. Scherer, Gudrun Rappold	2010	412
2	Haploinsufficiency of ARID1B, a Member of the SWI/SNF-A Chromatin-Remodeling Complex, Is a Frequent Cause of Intellectual Disability The American Journal of Human Genetics ·Juliane Hoyer, Arif B. Ekici, Sabine Endele, Bernt Popp, Christiane Zweier, Antje Wiesener, Eva Wohlleber, Andreas Dufke, Eva Rossier, Corinna Petsch, Markus Zweier, Ina Göhring, Alexander M. Zink, Gudrun Rappold, Evelin Schröck, Dagmar Wieczorek, Olaf Rieß, Hartmut Engels, Anita Rauch, André Reis	2012	174
3	Severe mental retardation with breathing abnormalities (Pitt–Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4 Human Molecular Genetics ·Antje Brockschmidt, Unda Todt, Soojin Ryu, Alexander Hoischen, Christina Landwehr, Stefanie Birnbaum, Wilhelm Frenck, Bernhard Radlwimmer, Peter Lichter, Hartmut Engels, Wolfgang Driever, Christian Kubisch, Ruthild G. Weber	2007	122
4	Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression Human Mutation ·Markus Zweier, Anne Gregor, Christiane Zweier, Hartmut Engels, Heinrich Sticht, Eva Wohlleber, Emilia K. Bijlsma, Susan Holder, Martin Zenker, Eva Rossier, Ute Grasshoff, Diana Johnson, Lisa Robertson, Helen V. Firth, Cornelia Kraus, Arif B. Ekici, André Reis, Anita Rauch	2010	115
5	Expression pattern and functional characteristics of two novel splice variants of the two‐pore‐domain potassium channel TREK‐2 The Journal of Physiology ·Wenli Gu, Günter Schlichthörl, Jochen R. Hirsch, Hartmut Engels, Christine Karschin, Andreas Karschin, Christian Derst, Ortrud K. Steinlein, Jürgen Daut	2002	88
6	Cantú Syndrome Resulting from Activating Mutation in theKCNJ8Gene Human Mutation ·Paige Cooper, Heiko Reutter, Joachim Woelfle, Hartmut Engels, Dorothy K. Grange, Gijs van Haaften, Bregje W.M. van Bon, Alexander Hoischen, Colin G. Nichols	2014	85
7	DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation Neurology ·Hartmut Engels, Antje Brockschmidt, Alexander Hoischen, Christina Landwehr, Kristin Bosse, Constanze Walldorf, Grischa Toedt, Bernhard Radlwimmer, Peter Propping, Peter Lichter, Ruthild G. Weber	2007	73
8	A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients European Journal of Human Genetics ·Hartmut Engels, Eva Wohlleber, Alexander M. Zink, Juliane Hoyer, Kerstin U. Ludwig, Felix F. Brockschmidt, Dagmar Wieczorek, Ute Moog, Birgit Hellmann-Mersch, Ruthild G. Weber, Lionel Willatt, Martina Kreiß‐Nachtsheim, Helen V. Firth, Anita Rauch	2009	70
9	Chromatin-Remodeling-Factor ARID1B Represses Wnt/β-Catenin Signaling The American Journal of Human Genetics ·Georgia Vasileiou, Arif B. Ekici, Steffen Uebe, Christiane Zweier, Juliane Hoyer, Hartmut Engels, Jürgen Behrens, André Reis, Michel V. Hadjihannas	2015	64
10	Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new cases Clinical Genetics ·Katja Eggermann, UA Mau, G Bujdosó, Erika Koltai, Hartmut Engels, Regine Schubert, Thomas Eggermann, Ruth Raff, Gesa Schwanitz	2002	56
11	Homozygous mutations in caveolin‐3 cause a severe form of rippling muscle disease Annals of Neurology ·Christian Kubisch, Benedikt Schoser, Monika von Düring, Regina C. Betz, Hans‐Hilmar Goebel, Susanne Zahn, Antje Ehrbrecht, Jan Aasly, Anja Schroers, Nikola Popović, Hanns Lochmüller, J. M. Schröder, Thomas Brüning, J.-P. Malin, B. Fricke, Hans‐Michael Meinck, T. Torbergsen, Hartmut Engels, B. Voß, Matthias Vorgerd	2003	51
12	Delineation of supernumerary marker chromosomes in 38 patients American Journal of Medical Genetics ·Renate Viersbach, Hartmut Engels, Ulrike Gamerdinger, M. Hansmann	1998	49
13	Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin–Siris syndrome-like phenotype Human Genetics ·Nuria C. Bramswig, Oana Caluseriu, H.‐J. Lüdecke, François V. Bolduc, Nicole C. L. Noel, Thomas Wieland, Harald Surowy, H.‐J. Christen, Hartmut Engels, Tim M. Strom, Dagmar Wieczorek	2017	46
14	Genetic counseling in Robertsonian translocations der(13;14): Frequencies of reproductive outcomes and infertility in 101 pedigrees American Journal of Medical Genetics Part A ·Hartmut Engels, Thomas Eggermann, Almuth Caliebe, Anna Jelska, Regine Schubert, Herdit M. Schüler, Barbara Panasiuk, Jacek Zaremba, Anna Latos‐Bieleńska, Lucjusz Jakubowski, Klaus Zerres, Gesa Schwanitz, Alina T. Midro	2008	45
15	Towards mapping phenotypical traits in 18p− syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation European Journal of Human Genetics ·Christian H Brenk, Eva‐Christina Prott, Detlef Trost, Alexander Hoischen, Constanze Walldorf, Bernhard Radlwimmer, Dagmar Wieczorek, Peter Propping, Gabriele Gillessen‐Kaesbach, Ruthild G. Weber, Hartmut Engels	2006	38
16	A de novo deletion of chromosome 5q causing familial adenomatous polyposis, dysmorphic features, and mild mental retardation The American Journal of Gastroenterology ·Jochen Raedle, Waltraut Friedl, Hartmut Engels, Rainer Koenig, (unknown), Stefan Zeuzem	2001	37
17	The phenotypic spectrum of duplication 5q35.2–q35.3 encompassing NSD1: Is it really a reversed sotos syndrome? American Journal of Medical Genetics Part A ·Nicola Dikow, Bianca Maas, Harald Gaspar, Martina Kreiß‐Nachtsheim, Hartmut Engels, Alma Kuechler, Lutz Garbes, Christian Netzer, Teresa Neuhann, Udo Koehler, Kristina Casteels, Koenraad Devriendt, Johannes W.G. Janssen, Anna Jauch, Katrin Hinderhofer, Ute Moog	2013	35
18	Loss-of-function variants in HIVEP2 are a cause of intellectual disability European Journal of Human Genetics ·Siddharth Srivastava, Hartmut Engels, Ina Schanze, Kirsten Cremer, Thomas Wieland, Moritz Menzel, (unknown), Saskia Biskup, Martina Kreiß, Sabine Endele, Tim M. Strom, Dagmar Wieczorek, Martin Zenker, Siddharth Gupta, Julie S. Cohen, Alexander M. Zink, Sakkubai Naidu	2015	33
19	Comprehensive review of the duplication 3q syndrome and report of a patient with Currarino syndrome and de novo duplication 3q26.32‐q27.2 Clinical Genetics ·Gabriel C. Dworschak, Célia Cretolle, Alina C. Hilger, Hartmut Engels, Eckhard Korsch, Heiko Reutter, Michael Ludwig	2016	32
20	A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype Journal of Medical Genetics ·Christiane Zweier, Cornelia Kraus, Louise Brueton, Trevor Cole, Franziska Degenhardt, Hartmut Engels, Gabriele Gillessen‐Kaesbach, Luitgard Graul‐Neumann, Denise Horn, Juliane Hoyer, Walter Just, Anita Rauch, André Reis, Bernd Wollnik, Michael Zeschnigk, Hermann‐Josef Lüdecke, Dagmar Wieczorek	2013	32

About Hartmut Engels

Hartmut Engels is a scholar working on Genetics, Molecular Biology, Plant Science, Surgery and Pediatrics, Perinatology and Child Health, having authored 66 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (34 papers), Genetics and Neurodevelopmental Disorders (17 papers), Chromosomal and Genetic Variations (15 papers), Congenital heart defects research (9 papers), Prenatal Screening and Diagnostics (7 papers), Genomics and Rare Diseases (5 papers), Genetic Syndromes and Imprinting (5 papers) and Ion channel regulation and function (5 papers). The work is most often cited by research in Genetics (1.2k citations), Molecular Biology (1.2k citations), Cognitive Neuroscience (297 citations), Developmental Neuroscience (58 citations) and Pediatrics, Perinatology and Child Health (208 citations). Hartmut Engels has collaborated with scholars based in Germany, Poland and United Kingdom. Frequent co-authors include Gesa Schwanitz, Dagmar Wieczorek, Gudrun Rappold, Ute Moog, Alexander Hoischen, Ruthild G. Weber, Volker Endris, Eva Wohlleber, Ralph Roeth and Simone Berkel. Their work appears in journals such as Human Genetics, European Journal of Human Genetics, European Journal of Medical Genetics, Human Mutation and The American Journal of Human 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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Hartmut Engels

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