Kerstin U. Ludwig

11.7k citations

85 papers · 2.0k indexed · h-index 27

Endocrinology top 1%
- Escherichia coli research studies 11
Genetics top 2%
- Cleft Lip and Palate Research 41
- Craniofacial Disorders and Treatments 30
- Congenital Ear and Nasal Anomalies 12
- Genomic variations and chromosomal abnormalities 11
Genetics top 5%
- Cleft Lip and Palate Research 41
- Craniofacial Disorders and Treatments 30
- Congenital Ear and Nasal Anomalies 12
- Genomic variations and chromosomal abnormalities 11
Infectious Diseases top 5%
- Viral gastroenteritis research and epidemiology 9
Developmental and Educational Psychology top 5%
- Reading and Literacy Development 10
Molecular Biology
- dental development and anomalies 8

Co-authors: Elisabeth Mangold Markus M. Nöthen Martin Bitzan Dirk E. Müller‐Wiefel Helge Karch Per Hoffmann Michael Knapp D. E. Müller‐Wiefel
Cited by: Endocrinology Genetics
Journals: SHILAP Revista de lepidopterología (1 paper)Bioinformatics (2 papers)Development (1 paper)
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

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

All Works

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20 of 20 papers shown

#	Work
1	Genetic heterogeneity and homogeneity among orofacial cleft subtypes: genome-wide association studies in the cleft collective Human Molecular Genetics ·Kyle Dack,Kerstin U. Ludwig,Evie Stergiakouli,Jonathan Sandy,Sethlina Naa Dodua Aryee,George Davey Smith,Amy Davies,Yvonne Wren,Gemma C. Sharp,Kerry Humphries,Elisabeth Mangold,Lucy J. Goudswaard,Karen Ho,Tom Dudding,Sarah J. Lewis	2025	0
2	Social cognitive bias increases loneliness both directly and by decreasing social connection in patients with schizophrenia Schizophrenia Research ·Łukasz Okruszek,Aleksandra Piejka,Marta Chrustowicz,Małgorzata Krawczyk,Michał Jarkiewicz,Anna Schudy,Kerstin U. Ludwig,Amy E. Pinkham	2023	9
3	Loneliness is associated with mentalizing and emotion recognition abilities in schizophrenia, but only in a cluster of patients with social cognitive deficits Journal of the International Neuropsychological Society ·Łukasz Okruszek,Michał Jarkiewicz,Aleksandra Piejka,Marta Chrustowicz,Małgorzata Krawczyk,Anna Schudy,Philip D. Harvey,David L. Penn,Kerstin U. Ludwig,M. F. Green,A. E. Pinkham	2023	6
4	Predicting the pathogenicity of missense variants using features derived from AlphaFold2 Bioinformatics ·Axel Schmidt,Sebastian Röner,Karola Mai,Hannah Klinkhammer,Martin Kircher,Kerstin U. Ludwig	2023	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 Human Genetics and Genomics Advances ·Hanna K. Zieger,Leonie Weinhold,Axel Schmidt,Manuel Holtgrewe,Stefan Juranek,Anna Siewert,Annika B. Scheer,Frederic Thieme,Elisabeth Mangold,Nina Ishorst,Fabian Brand,Julia Welzenbach,Dieter Beule,Katrin Paeschke,Peter Krawitz,Kerstin U. Ludwig	2022	2
6	Iron Deficiency Caused by Intestinal Iron Loss—Novel Candidate Genes for Severe Anemia Genes ·Carolina Huettmann,Matthias Stelljes,Sugirthan Sivalingam,Manfred Fobker,Alexis Vrachimis,Anne Exler,Christian Wenning,Carola Wempe,Matthias Penke,Andreas Buneß,Kerstin U. Ludwig,Martina U. Muckenthaler,Andrea U. Steinbicker	2021	3
7	Cleft lip/palate and educational attainment: cause, consequence or correlation? A Mendelian randomization study International Journal of Epidemiology ·Christina Dardani,Laurence J Howe,Nandita Mukhopadhyay,Evie Stergiakouli,Yvonne Wren,Kerry Humphries,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	2020	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 Genes ·Iris A.L.M. van Rooij,Kerstin U. Ludwig,Julia Welzenbach,Nina Ishorst,Michelle Thonissen,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	2019	13
9	Investigation of dominant and recessive inheritance models in genome‐wide association studies data of nonsyndromic cleft lip with or without cleft palate 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	2017	6
10	Further evidence for genetic variation at the serotonin transporter gene SLC6A4 contributing toward anxiety Psychiatric Genetics ·Andreas J. Forstner,Stefanie Rambau,Nina Friedrich,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	2017	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 PLoS Genetics ·Kerstin U. Ludwig,Syeda Ahmed,Anne C. Böhmer,Nasim Bahram Sangani,Sheryil Varghese,Johanna Klamt,Hannah Schuenke,Pınar Gültepe,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	2016	60
12	A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults 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	2013	24
13	Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study 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	2013	112
14	Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling 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	2012	17
15	Breakthroughs in the genetics of orofacial clefting Trends in Molecular Medicine ·Elisabeth Mangold,Kerstin U. Ludwig,Markus M. Nöthen	2011	96
16	First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children 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	2009	77
17	Escherichia coliO157 Fails to Induce a Long‐Lasting Lipopolysaccharide‐Specific, Measurable Humoral Immune Response in Children with Hemolytic‐Uremic Syndrome The Journal of Infectious Diseases ·Kerstin U. Ludwig,Martin Bitzan,Christoph Bobrowski,Dirk E. Müller‐Wiefel	2002	20
18	Pathomechanisms in the haemolytic-uraemic syndrome Nephrology Dialysis Transplantation ·Kerstin U. Ludwig,D. E. Müller‐Wiefel	1998	7
19	The role of Escherichia coli O 157 infections in the classical (enteropathic) haemolytic uraemic syndrome: Results of a Central European, multicentre study Epidemiology and Infection ·Martin Bitzan,Kerstin U. Ludwig,M. Klemt,H. König,Jonas Burén,D. E. Müller‐Wiefel	1993	99
20	High incidence of serum antibodies to Escherichia coli O157 lipopolysaccharide in children with hemolytic-uremic syndrome The Journal of Pediatrics ·Martin Bitzan,Eckehard Moebius,Kerstin U. Ludwig,Dirk E. Müller‐Wiefel,Jürgen Heesemann,Helge Karch	1991	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), Congenital Ear and Nasal Anomalies (12 papers), Escherichia coli research studies (11 papers), Genomic variations and chromosomal abnormalities (11 papers), Reading and Literacy Development (10 papers), Viral gastroenteritis research and epidemiology (9 papers) and dental development and anomalies (8 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.

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