Hartmut Engels

7.0k citations

66 papers · 2.2k indexed · h-index 25

Impact in

Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Molecular Biology top 5%
- Congenital heart defects research
- Chromatin Remodeling and Cancer

Papers in

Genetics 46
- Genomic variations and chromosomal abnormalities 37
- Genetics and Neurodevelopmental Disorders 18
- Genetic Syndromes and Imprinting 5
- Genomics and Rare Diseases 5
Developmental Biology 3

Co-authors: Gesa Schwanitz Gudrun Rappold Dagmar Wieczorek Ute Moog Alexander Hoischen Ruthild G. Weber Péter Szatmári Stephen W. Scherer
Journals: European Journal of Human Genetics (7 papers)Human Genetics (7 papers)European Journal of Medical Genetics (3 papers)Human Mutation (3 papers)Prenatal Diagnosis (2 papers)
Partner nations: Germany United Kingdom Poland

In The Last Decade

Hartmut Engels

64 papers receiving 2.1k 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-authorship network

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

#	Work
1	Variants in FGF10 cause early onset of severe childhood interstitial lung disease: A detailed description of four affected children Pediatric Pulmonology ·مریم شریفیان ثانی, Axel Schmidt, Nicolaus Schwerk, Diane M. Renz, Bénédicte Gérard, Élise Schaefer, Maria Cristina Antal, Sophia Peters, Matthias Griese, Christina Rapp, Hartmut Engels, Kirsten Cremer, Anke K. Bergmann, Gunnar Schmidt, Bernd Auber, Jan C. Kamp, Florian Laenger, Sandra von Hardenberg	2023	7
2	Congenital diaphragmatic hernia in a case of Cat eye syndrome Clinical Case Reports ·Radosław Pastusiak, Heiko Reutter, Soyhan Bağcı, Florian Kipfmueller, Hartmut Engels, Ramesh Bhonde, Elisabeth Mangold, U. Gembruch, Annegret Geipel, Andreas Müller, T Schaible	2018	4
3	De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies Human Genetics ·Jeff Schein, Alma Kuechler, Mona Grimmel, Jessica Becker, Sophia Peters, Marc Sturm, M. García‐Sandoval, Axel Schmidt, Martina Kreiß, Tim M. Strom, Dagmar Wieczorek, Tobias B. Haack, Stefanie Beck‐Wödl, Kirsten Cremer, Hartmut Engels	2018	16
4	De novo microdeletions and point mutations affecting SOX2 in three individuals with intellectual disability but without major eye malformations American Journal of Medical Genetics Part A ·Anggi Kurnianto, Hartmut Engels, Kirsten Cremer, Jessica Becker, Eva Wohlleber, Beate Albrecht, T. F. TOUT, Hermann‐Josef Lüdecke, Mohnish Suri, Ramesh Allipour-Birgani, Alessandra Renieri, Guido Kukuk, Thomas Wieland, Joris Andrieux, Tim M. Strom, Dagmar Wieczorek, Anne Dieux‐Coëslier, Alexander M. Zink	2016	13
5	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, Max Schubach, Saskia Biskup, Martina Kreiß, Sabine Endele, Tim M. Strom, Dagmar Wieczorek, Martin Zenker, Siddharth Gupta, Julie S. Cohen, Alexander M. Zink, Sakkubai Naidu	2015	31
6	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
7	Microdeletions Including FMR1 in Three Female Patients with Intellectual Disability - Further Delineation of the Phenotype and Expression Studies Molecular Syndromology ·Alexander M. Zink, Eva Wohlleber, Hartmut Engels, Olaug K. Rødningen, Kirstine Ravn, Stefanie Heilmann‐Heimbach, Anta Rini Utami, Andreas Jansson, Cornelia Kraus, Susanne Blichfeldt, Per Hoffmann, Heiko Reutter, F.F. Brockschmidt, Martina Kreiß‐Nachtsheim, P. H. Vogt, Trine Prescott, Zeynep Tümer, Bangtang Chen	2014	6
8	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, 张明宪, 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
9	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
10	Dissecting the genotype in syndromic intellectual disability using whole exome sequencing in addition to genome-wide copy number analysis Human Genetics ·Carl Friedrich Classen, Vera Riehmer, Christina Landwehr, Maria Magdalena Fitri, Stefanie Heilmann‐Heimbach, Caroline Scholz, 张万栋, Hartmut Engels, Sascha Tierling, Miroslav Živičnjak, Frank Schacherer, Dieter Haffner, Ruthild G. Weber	2013	18
11	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, 稔土肥, Markus Zweier, F Fernández-Melchor, Alexander M. Zink, Gudrun Rappold, Evelin Schröck, Dagmar Wieczorek, Olaf Rieß, Hartmut Engels, Anita Rauch, André Reis	2012	173
12	Five patients with novel overlapping interstitial deletions in 8q22.2q22.3 American Journal of Medical Genetics Part A ·Alma Kuechler, Karen Buysse, Jill Clayton‐Smith, Cédric Le Caignec, Albert David, Hartmut Engels, Jürgen Kohlhase, Francesca Mari, Geert Mortier, Alessandra Renieri, Dagmar Wieczorek	2011	22
13	Clinical and molecular characterization of two patients with overlapping de novo microdeletions in 2p14-p15 and mild mental retardation European Journal of Medical Genetics ·Eva Wohlleber, Maria Kirchhoff, Alexander M. Zink, Martina Kreiß‐Nachtsheim, ناصر بن محمد الصائغ, Birgit Jepsen, Susanne Kjærgaard, Hartmut Engels	2010	10
14	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, 서상준, Ruthild G. Weber, Lionel Willatt, Martina Kreiß‐Nachtsheim, Helen V. Firth, Anita Rauch	2009	68
15	Angeborene kardiovaskuläre Fehlbildungen und chromosomale Mikrodeletionen in 22q11.2 DMW - Deutsche Medizinische Wochenschrift ·有二渡辺, Hartmut Engels, Gerhard Bauriedel, Dinara Has'yanova, Gesa Schwanitz	2008	5
16	Genome‐wide analysis for micro‐aberrations in familial exstrophy of the bladder using array‐based comparative genomic hybridization British Journal of Urology ·Heiko Reutter, Alexander Hoischen, Michael Ludwig, Raimund Stein, Bernhard Radlwimmer, Hartmut Engels, Katja P. Wolffenbuttel, Ruthild G. Weber	2007	6
17	Further delineation of the phenotype maps for partial trisomy 16q24 and Jacobsen syndrome by a subtle familial translocation t(11;16)(q24.2;q24.1) American Journal of Medical Genetics Part A ·Susanne Zahn, Moazzma Ahmed, Kristin Bosse, Vera M. Kalscheuer, Peter Propping, Gesa Schwanitz, Beate Albrecht, Hartmut Engels	2005	15
18	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
19	Further case of Cantú syndrome: Exclusion of cryptic subtelomeric chromosome aberrations American Journal of Medical Genetics ·Hartmut Engels, Kristin Bosse, Moazzma Ahmed, Susanne Zahn, Alexander Hoischen, Peter Propping, L. Bindl, Heiko Reutter	2002	17
20	Delineation of supernumerary marker chromosomes in 38 patients American Journal of Medical Genetics ·Eszter Szlávich, Hartmut Engels, Ulrike Gamerdinger, M. Hansmann	1998	49

About Hartmut Engels

Hartmut Engels is a scholar working on Genetics, Developmental Biology, Pediatrics, Perinatology and Child Health, Molecular Biology and Plant Science, having authored 66 papers that have together received 2.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (37 papers), Genetics and Neurodevelopmental Disorders (18 papers), Chromosomal and Genetic Variations (15 papers), Congenital heart defects research (9 papers), Prenatal Screening and Diagnostics (8 papers), Genetic Syndromes and Imprinting (5 papers), Genomics and Rare Diseases (5 papers) and Chromatin Remodeling and Cancer (5 papers). The work is most often cited by research in Genetics (1.3k citations), Molecular Biology (1.3k citations), Cognitive Neuroscience (326 citations), Developmental Neuroscience (69 citations) and Pediatrics, Perinatology and Child Health (267 citations). Hartmut Engels has collaborated with scholars based in Germany, United Kingdom and Poland. Frequent co-authors include Gesa Schwanitz, Gudrun Rappold, Dagmar Wieczorek, Ute Moog, Alexander Hoischen, Ruthild G. Weber, Péter Szatmári, Stephen W. Scherer, Simone Berkel and Dalila Pinto. Their work appears in journals such as European Journal of Human Genetics, Human Genetics, European Journal of Medical Genetics, Human Mutation and Prenatal Diagnosis.

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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