Elisabeth Mangold

10.5k citations

117 papers · 4.0k indexed · h-index 36

Pathology and Forensic Medicine top 0.5%
Molecular Biology top 5%
Genetics top 1%
Oncology top 2%
Cancer Research top 2%

Co-authors: Peter Propping Waltraut Friedl Constanze Pagenstecher Kerstin U. Ludwig Stefan Aretz Siegfried Uhlhaas Markus M. Nöthen Gabriela Möslein
Topics: Cleft Lip and Palate Research (48 papers)Genetic factors in colorectal cancer (39 papers)Craniofacial Disorders and Treatments (36 papers)
Cited by: Pathology and Forensic Medicine Cancer Research Genetics
Journals: Journal of Clinical OncologySHILAP Revista de lepidopterologíaBioinformatics
Partner nations: Germany United States United Kingdom

In The Last Decade

Elisabeth Mangold

113 papers receiving 3.9k citations

Peers

Countries citing papers authored by Elisabeth Mangold

Since Specialization

Citations

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

Fields of papers citing papers by Elisabeth Mangold

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabeth Mangold

This figure shows the co-authorship network connecting the top 25 collaborators of Elisabeth Mangold. A scholar is included among the top collaborators of Elisabeth Mangold 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 Elisabeth Mangold. Elisabeth Mangold is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Genetic heterogeneity and homogeneity among orofacial cleft subtypes: genome-wide association studies in the cleft collective 2025 ·Human Molecular Genetics ·(unknown),Kerstin U. Ludwig,Evie Stergiakouli,Jonathan Sandy,(unknown),George Davey Smith,Amy Davies,Yvonne Wren,Gemma C. Sharp,(unknown),Elisabeth Mangold,(unknown),Karen Ho,Tom Dudding,Sarah J. Lewis	0
2	Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of de novo mutations 2022 ·Human Genetics and Genomics Advances ·(unknown),Leonie Weinhold,Axel Schmidt,Manuel Holtgrewe,Stefan Juranek,(unknown),(unknown),(unknown),Elisabeth Mangold,Nina Ishorst,(unknown),(unknown),Dieter Beule,Katrin Paeschke,Peter Krawitz,Kerstin U. Ludwig	2
3	Cleft lip/palate and educational attainment: cause, consequence or correlation? A Mendelian randomization study 2020 ·International Journal of Epidemiology ·Christina Dardani,Laurence J Howe,Nandita Mukhopadhyay,Evie Stergiakouli,Yvonne Wren,(unknown),Amy Davies,Karen Ho,Seth M. Weinberg,Mary L. Marazita,Elisabeth Mangold,Kerstin U. Ludwig,Caroline L. Relton,George Davey Smith,Sarah J. Lewis,Jonathan Sandy,Neil M Davies,Gemma C. Sharp	23
4	Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene 2019 ·Genes ·Iris A.L.M. van Rooij,Kerstin U. Ludwig,(unknown),Nina Ishorst,(unknown),Tessel E. Galesloot,Edwin M. Ongkosuwito,Stefaan Bergé,Khalid Aldhorae,Augusto Rojas-Martı́nez,Lambertus A. Kiemeney,Joris Vermeesch,Han G. Brunner,Nel Roeleveld,Koenraad Devriendt,Titiaan Dormaar,Greet Hens,Michael Knapp,Carine Carels,Elisabeth Mangold	13
5	The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1 2018 ·Investigative Ophthalmology & Visual Science ·Imran H. Yusuf,Martin Gliem,Johannes Birtel,Philipp L. Müller,Elisabeth Mangold,(unknown),Peter Charbel Issa	1
6	Congenital diaphragmatic hernia in a case of Cat eye syndrome 2018 ·Clinical Case Reports ·(unknown),Heiko Reutter,Soyhan Bağcı,Florian Kipfmueller,Hartmut Engels,(unknown),Elisabeth Mangold,U. Gembruch,Annegret Geipel,Andreas Müller,T Schaible	4
7	Investigation of dominant and recessive inheritance models in genome‐wide association studies data of nonsyndromic cleft lip with or without cleft palate 2017 ·Birth Defects Research ·Anne C. Böhmer,Lina Gölz,Thomas Kreusch,Franz‐Josef Kramer,Bernd Pötzsch,Markus M. Nöthen,Andreas Jäger,Elisabeth Mangold,Michael Knapp,Kerstin U. Ludwig	6
8	Novel Insights Into the Phenotypical Spectrum of KIF11 -Associated Retinopathy, Including a New Form of Retinal Ciliopathy 2017 ·Investigative Ophthalmology & Visual Science ·Johannes Birtel,Martin Gliem,Elisabeth Mangold,Lars Tebbe,Isabel Spier,Philipp L. Müller,Frank G. Holz,Christine Neuhaus,Uwe Wolfrum,Hanno J. Bolz,Peter Charbel Issa	47
9	Further evidence for genetic variation at the serotonin transporter gene SLC6A4 contributing toward anxiety 2017 ·Psychiatric Genetics ·Andreas J. Forstner,(unknown),(unknown),Kerstin U. Ludwig,Anne C. Böhmer,Elisabeth Mangold,Anna Maaser,Timo Hess,Alexandra Kleiman,Antje Bittner,Markus M. Nöthen,Jessica Becker,Franziska Geiser,Johannes Schumacher,Rupert Conrad	24
10	Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene 2016 ·PLoS Genetics ·Kerstin U. Ludwig,(unknown),Anne C. Böhmer,(unknown),(unknown),(unknown),(unknown),(unknown),Andrea Hofmann,Michele Rubini,Khalid Aldhorae,Régine P.M. Steegers‐Theunissen,Augusto Rojas-Martı́nez,Rudolf Reiter,Guntram Borck,Michael Knapp,Mitsushiro Nakatomi,Daniel Graf,Elisabeth Mangold,Heiko Peters	60
11	Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study 2013 ·Human Genetics ·Terri H. Beaty,Margaret A. Taub,Alan F. Scott,Jeffrey C. Murray,Mary L. Marazita,Holger Schwender,Margaret M. Parker,Jacqueline B. Hetmanski,Poojitha Balakrishnan,M. Adela Mansilla,Elisabeth Mangold,Kerstin U. Ludwig,Markus M. Nöethen,Michele Rubini,Nursel Elcioğlu,Ingo Ruczinski	112
12	The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families 2012 ·Clinical Genetics ·Manuela Pinheiro,Carla Pinto,Ana Peixoto,Isabel Veiga,Bárbara Mesquita,Rui Henrique,Paula Lopes,(unknown),Maria Fragoso,(unknown),(unknown),(unknown),Elisabeth Mangold,Carlos Vaccaro,D. Gareth Evans,Susan M. Farrington,(unknown),(unknown)	11
13	Breakthroughs in the genetics of orofacial clefting 2011 ·Trends in Molecular Medicine ·Elisabeth Mangold,Kerstin U. Ludwig,Markus M. Nöthen	96
14	Compound heterozygosity for two MSH6 mutations in a patient with early onset colorectal cancer, vitiligo and systemic lupus erythematosus 2008 ·American Journal of Medical Genetics Part A ·Nils Rahner,Gerald Höefler,Christoph Högenauer,C. Lackner,Verena Steinke,(unknown),Waltraut Friedl,Stefan Aretz,Peter Propping,Elisabeth Mangold,Constanze Walldorf	34
15	Pathogenicity of MSH2 Missense Mutations Is Typically Associated With Impaired Repair Capability of the Mutated Protein 2006 ·Gastroenterology ·Saara Ollila,Laura Sarantaus,Reetta Kariola,Philip A. Chan,Heather Hampel,Elke Holinski‐Feder,Finlay Macrae,Maija R.J. Kohonen‐Corish,Anne‐Marie Gerdes,Païvi Peltomäki,Elisabeth Mangold,Albert de la Chapelle,Marc S. Greenblatt,Minna Nyström	54
16	MSH6 mutation in Muir?Torre syndrome: could this be a rare finding? 2006 ·British Journal of Dermatology ·Elisabeth Mangold,Nils Rahner,Nicolaus Friedrichs,Reinhard Buettner,Constanze Pagenstecher,Stefan Aretz,Waltraut Friedl,Thomas Ruzicka,Peter Propping,Arno Rütten,Roland Kruse	26
17	Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer 2005 ·International Journal of Cancer ·Christoph Engel,(unknown),Elke Holinski‐Feder,Constanze Pagenstecher,Jens Plaschke,Matthias Kloor,Christopher Poremba,Christian Pox,Josef Rüschoff,Gisela Keller,Wolfgang Dietmaier,Petra Rümmele,Nicolaus Friedrichs,Elisabeth Mangold,Reinhard Buettner,Hans K. Schackert,Peter Kienle,Susanne Stemmler,Gabriela Möslein,Markus Loeffler	71
18	Stromal expression of invasion‐promoting, matrix‐degrading proteases MMP‐1 and ‐9 and the Ets 1 transcription factor in HNPCC carcinomas and sporadic colorectal cancers 2003 ·International Journal of Cancer ·Peter Behrens,Micaela Mathiak,Elisabeth Mangold,(unknown),Axel Wellmann,Franz Fogt,Marcus Rothe,Alexandra Florin,Nicolas Wernert	48
19	A modified multiplex PCR assay for detection of large deletions inMSH2 andMLH1 2002 ·Human Mutation ·Yaping Wang,Waltraut Friedl,(unknown),Matthias Jungck,Isabel Filges,Peter Propping,Elisabeth Mangold	31
20	DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2 2001 ·Journal of Biochemical and Biophysical Methods ·Elke Holinski‐Feder,(unknown),Waltraut Friedl,Gabriela Möslein,Gisela Keller,Jens Plaschke,Wolfgang G. Ballhausen,(unknown),(unknown),Matthias Jungck,Elisabeth Mangold,H. Vogelsang,Hans K. Schackert,(unknown),Jan Murken,Thomas Meitinger	82

About Elisabeth Mangold

Elisabeth Mangold is a scholar working on Genetics, Pathology and Forensic Medicine and Cancer Research, having authored 117 papers that have together received 4.0k indexed citations. Recurring topics across this work include Cleft Lip and Palate Research (48 papers), Genetic factors in colorectal cancer (39 papers) and Craniofacial Disorders and Treatments (36 papers). The work is most often cited by research in Pathology and Forensic Medicine (1.9k citations), Cancer Research (1.0k citations) and Genetics (1.4k citations). Elisabeth Mangold has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Peter Propping, Waltraut Friedl, Constanze Pagenstecher, Kerstin U. Ludwig, Stefan Aretz, Siegfried Uhlhaas, Markus M. Nöthen, Gabriela Möslein, Micaela Mathiak and Karsten Schulmann. Their work appears in journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Bioinformatics.

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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