Kerstin U. Ludwig

11.7k citations

85 papers · 2.0k indexed · h-index 27

Genetics top 2%
Molecular Biology
Endocrinology top 1%
Infectious Diseases top 5%
Developmental and Educational Psychology top 5%

Co-authors: Elisabeth Mangold Markus M. Nöthen Martin Bitzan Dirk E. Müller‐Wiefel Helge Karch Per Hoffmann Michael Knapp D. E. Müller‐Wiefel
Topics: Cleft Lip and Palate Research (41 papers)Craniofacial Disorders and Treatments (30 papers)Congenital Ear and Nasal Anomalies (12 papers)
Cited by: Endocrinology Genetics
Journals: SHILAP Revista de lepidopterologíaBioinformatics Development
Partner nations: Germany United States United Kingdom

In The Last Decade

Kerstin U. Ludwig

81 papers receiving 2.0k citations

Peers

Countries citing papers authored by Kerstin U. Ludwig

Since Specialization

Citations

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

Fields of papers citing papers by Kerstin U. Ludwig

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kerstin U. Ludwig. 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 Kerstin U. Ludwig. The network helps show where Kerstin U. Ludwig may publish in the future.

Co-authorship network of co-authors of Kerstin U. Ludwig

This figure shows the co-authorship network connecting the top 25 collaborators of Kerstin U. Ludwig. A scholar is included among the top collaborators of Kerstin U. Ludwig 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 Kerstin U. Ludwig. Kerstin U. Ludwig 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	Social cognitive bias increases loneliness both directly and by decreasing social connection in patients with schizophrenia 2023 ·Schizophrenia Research ·Łukasz Okruszek,Aleksandra Piejka,(unknown),(unknown),Michał Jarkiewicz,(unknown),Kerstin U. Ludwig,Amy E. Pinkham	9
3	Loneliness is associated with mentalizing and emotion recognition abilities in schizophrenia, but only in a cluster of patients with social cognitive deficits 2023 ·Journal of the International Neuropsychological Society ·Łukasz Okruszek,Michał Jarkiewicz,Aleksandra Piejka,(unknown),(unknown),(unknown),Philip D. Harvey,David L. Penn,Kerstin U. Ludwig,M. F. Green,(unknown)	6
4	Predicting the pathogenicity of missense variants using features derived from AlphaFold2 2023 ·Bioinformatics ·Axel Schmidt,Sebastian Röner,(unknown),Hannah Klinkhammer,Martin Kircher,Kerstin U. Ludwig	35
5	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
6	Iron Deficiency Caused by Intestinal Iron Loss—Novel Candidate Genes for Severe Anemia 2021 ·Genes ·(unknown),Matthias Stelljes,Sugirthan Sivalingam,Manfred Fobker,Alexis Vrachimis,(unknown),Christian Wenning,Carola Wempe,(unknown),Andreas Buneß,Kerstin U. Ludwig,Martina U. Muckenthaler,Andrea U. Steinbicker	3
7	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
8	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
9	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
10	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
11	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
12	A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults 2013 ·Translational Psychiatry ·Kerstin U. Ludwig,Philipp G. Sämann,Michael P. Alexander,Jessica Becker,Jennifer Bruder,Kristina Moll,Derek Spieler,Michael Czisch,Andreas Warnke,Sophia Docherty,Oliver S. P. Davis,Robert Plomin,Markus M. Nöthen,Karin Landerl,Bertram Müller‐Myhsok,Per Hoffmann,J Schumacher,Gerd Schulte‐Körne,Darina Czamara	24
13	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
14	Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling 2012 ·Translational Psychiatry ·Jessica Becker,Darina Czamara,Per Hoffmann,Karin Landerl,Leo Blomert,Daniel Brandeis,Anniek Vaessen,Urs Maurer,Kristina Moll,Kerstin U. Ludwig,Bertram Müller‐Myhsok,Markus M. Nöthen,Gerd Schulte‐Körne,J Schumacher	17
15	Breakthroughs in the genetics of orofacial clefting 2011 ·Trends in Molecular Medicine ·Elisabeth Mangold,Kerstin U. Ludwig,Markus M. Nöthen	96
16	First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children 2009 ·Molecular Psychiatry ·Darina Roeske,Kerstin U. Ludwig,Nina Neuhoff,Jessica Becker,Jürgen Bartling,Jennifer Bruder,F.F. Brockschmidt,Andreas Warnke,Helmut Remschmidt,Per Hoffmann,Bertram Müller‐Myhsok,Markus M. Nöthen,Gerd Schulte‐Körne	77
17	Escherichia coliO157 Fails to Induce a Long‐Lasting Lipopolysaccharide‐Specific, Measurable Humoral Immune Response in Children with Hemolytic‐Uremic Syndrome 2002 ·The Journal of Infectious Diseases ·Kerstin U. Ludwig,Martin Bitzan,Christoph Bobrowski,Dirk E. Müller‐Wiefel	20
18	Pathomechanisms in the haemolytic-uraemic syndrome 1998 ·Nephrology Dialysis Transplantation ·Kerstin U. Ludwig,D. E. Müller‐Wiefel	7
19	The role of Escherichia coli O 157 infections in the classical (enteropathic) haemolytic uraemic syndrome: Results of a Central European, multicentre study 1993 ·Epidemiology and Infection ·Martin Bitzan,Kerstin U. Ludwig,(unknown),H. König,Jonas Burén,D. E. Müller‐Wiefel	99
20	High incidence of serum antibodies to Escherichia coli O157 lipopolysaccharide in children with hemolytic-uremic syndrome 1991 ·The Journal of Pediatrics ·Martin Bitzan,(unknown),Kerstin U. Ludwig,Dirk E. Müller‐Wiefel,Jürgen Heesemann,Helge Karch	114

About Kerstin U. Ludwig

Kerstin U. Ludwig is a scholar working on Endocrinology, Genetics and Genetics, having authored 85 papers that have together received 2.0k indexed citations. Recurring topics across this work include Cleft Lip and Palate Research (41 papers), Craniofacial Disorders and Treatments (30 papers) and Congenital Ear and Nasal Anomalies (12 papers). The work is most often cited by research in Endocrinology (416 citations), Genetics (1.1k citations) and Genetics (228 citations). Kerstin U. Ludwig has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Elisabeth Mangold, Markus M. Nöthen, Martin Bitzan, Dirk E. Müller‐Wiefel, Helge Karch, Per Hoffmann, Michael Knapp, D. E. Müller‐Wiefel, Bertram Müller‐Myhsok and Gerd Schulte‐Körne. Their work appears in journals such as SHILAP Revista de lepidopterología, Bioinformatics and Development.

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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