Anne C. Böhmer

2.8k citations

21 papers · 536 indexed · h-index 14

Co-authors: Kerstin U. Ludwig Elisabeth Mangold Johannes Schumacher Michael Knapp Oliver Schildgen Jessica Lüsebrink Verena Schildgen Ramona Liza Tillmann
Topics: Cleft Lip and Palate Research (12 papers)Craniofacial Disorders and Treatments (10 papers)Congenital Ear and Nasal Anomalies (6 papers)
Cited by: Gastroenterology Genetics
Journals: PLoS ONE Gut Human Molecular Genetics
Partner nations: Germany Netherlands United Kingdom

In The Last Decade

Anne C. Böhmer

21 papers receiving 533 citations

Peers

Countries citing papers authored by Anne C. Böhmer

Since Specialization

Citations

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

Fields of papers citing papers by Anne C. Böhmer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anne C. Böhmer. 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 Anne C. Böhmer. The network helps show where Anne C. Böhmer may publish in the future.

Co-authorship network of co-authors of Anne C. Böhmer

This figure shows the co-authorship network connecting the top 25 collaborators of Anne C. Böhmer. A scholar is included among the top collaborators of Anne C. Böhmer 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 Anne C. Böhmer. Anne C. Böhmer 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	Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett’s oesophagus and provides insights into clinical heterogeneity in reflux diagnosis 2021 ·Gut ·Jue‐Sheng Ong,Jiyuan An,Xikun Han,Matthew H. Law,Priyanka Nandakumar,Johannes Schumacher,Ines Gockel,Anne C. Böhmer,Janusz Jankowski,Claire Palles,Catherine M. Olsen,Rachel Ε. Neale,Rebecca C. Fitzgerald,Aaron P. Thrift,Thomas L. Vaughan,Matthew F. Buas,(unknown),Puya Gharahkhani,Bradley J. Kendall,Stuart MacGregor	98
2	Innovationsunterstützung im BfArM – Erfahrungen aus den Beratungen zu digitalen Gesundheitsanwendungen (DiGA) 2021 ·Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz ·(unknown),Anne C. Böhmer,(unknown)	4
3	Strengthening regulatory science in academia: STARS, an EU initiative to bridge the translational gap 2020 ·Drug Discovery Today ·Viktoriia Starokozhko,Marko J. Kallio,(unknown),(unknown),(unknown),Mark Goldammer,Manja Burggraf,(unknown),Anne C. Böhmer,(unknown),Corinne S de Vries,Anna M.G. Pasmooij,Peter G. M. Mol	21
4	Genetic estimators of DNA methylation provide insights into the molecular basis of polygenic traits 2018 ·Translational Psychiatry ·Virginie Freytag,Vanja Vukojević,(unknown),Annette Milnik,Christian Vogler,Markus Leber,Leonie Weinhold,Anne C. Böhmer,Steffi G. Riedel‐Heller,Wolfgang Maier,Dominique J.‐F. de Quervain,Alfredo Ramı́rez,Andreas Papassotiropoulos	6
5	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
6	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
7	Imputation of Orofacial Clefting Data Identifies Novel Risk Loci and Sheds Light on the Genetic Background of Cleft Lip ± Cleft Palate and Cleft Palate Only. 2017 ·Human Molecular Genetics ·Kerstin U. Ludwig,Anne C. Böhmer,John Bowes,Miloš Nikolić,Nina Ishorst,(unknown),Nigel L. Hammond,Lina Gölz,(unknown),Sandra Barth,(unknown),(unknown),Malte Spielmann,Khalid Aldhorae,Augusto Rojas-Martı́nez,Markus M. Nöthen,Álvaro Rada-Iglesias,Michael J. Dixon,Michael Knapp,Elisabeth Mangold	66
8	Insights into the genetics of gastroesophageal reflux disease (GERD) and GERD‐related disorders 2017 ·Neurogastroenterology & Motility ·Anne C. Böhmer,Johannes Schumacher	19
9	Common variants in DLG1 locus are associated with non‐syndromic cleft lip with or without cleft palate 2017 ·Clinical Genetics ·Adrianna Mostowska,(unknown),Kacper Żukowski,Kerstin U. Ludwig,Kamil K. Hozyasz,Piotr Wójcicki,Elisabeth Mangold,Anne C. Böhmer,Stefanie Heilmann‐Heimbach,Michael Knapp,Małgorzata Zadurska,Barbara Biedziak,(unknown),(unknown),(unknown),Paweł P. Jagodzińśki	27
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	Nonsyndromic cleft lip with or without cleft palate and cancer: Evaluation of a possible common genetic background through the analysis of GWAS data 2016 ·Genomics Data ·(unknown),Kerstin U. Ludwig,Michael Knapp,Christine F. Skibola,Jane C. Figueiredo,Fay J. Hosking,Eva Ellinghaus,Maria Teresa Landi,Hongxia Ma,Hidewaki Nakagawa,Jong‐Won Kim,Jiali Han,Ping Yang,Anne C. Böhmer,Manuel Mattheisen,Markus M. Nöthen,Elisabeth Mangold	18
12	Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate 2016 ·Birth Defects Research Part A Clinical and Molecular Teratology ·(unknown),Andrea Hofmann,Anne C. Böhmer,(unknown),Lina Gölz,Jessica Becker,Alexander M. Zink,Markus Draaken,Alexander Hemprich,Martin Scheer,Gül Schmidt,Markus Martini,Michael Knapp,Elisabeth Mangold,Franziska Degenhardt,Kerstin U. Ludwig	5
13	Replication analysis of 15 susceptibility loci for nonsyndromic cleft lip with or without cleft palate in an italian population 2015 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Francesca Curà,Anne C. Böhmer,(unknown),(unknown),Luca Scapoli,Marcella Martinelli,Francesco Carinci,Markus M. Nöthen,Michael Knapp,Kerstin U. Ludwig,Elisabeth Mangold	9
14	Nonsyndromic cleft lip with or without cleft palate in arab populations: Genetic analysis of 15 risk loci in a novel case–control sample recruited in Yemen 2014 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Khalid Aldhorae,Anne C. Böhmer,Kerstin U. Ludwig,(unknown),Nezar N. Al‐Hebshi,(unknown),Lina Gölz,Markus M. Nöthen,Nikolaos Daratsianos,Michael Knapp,Andreas Jäger,Elisabeth Mangold	17
15	Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants withinGremlin‐1, a component of the bone morphogenetic protein 4 pathway 2014 ·Birth Defects Research Part A Clinical and Molecular Teratology ·(unknown),Kerstin U. Ludwig,Heide Fier,Bernd Pötzsch,Rudolf H. Reich,Gül Schmidt,Bert Braumann,Nikolaos Daratsianos,Anne C. Böhmer,(unknown),Margrieta A Alblas,Nadine Fricker,Per Hoffmann,Michael Knapp,Christoph Lange,Markus M. Nöthen,Elisabeth Mangold	18
16	Genome-wide analysis of parent-of-origin effects in non-syndromic orofacial clefts 2013 ·European Journal of Human Genetics ·Paras Garg,Kerstin U. Ludwig,Anne C. Böhmer,Michele Rubini,Régine P.M. Steegers‐Theunissen,Peter Mossey,Elisabeth Mangold,Andrew J. Sharp	12
17	Analysis of susceptibility loci for nonsyndromic orofacial clefting in a European trio sample 2013 ·American Journal of Medical Genetics Part A ·Anne C. Böhmer,Elisabeth Mangold,(unknown),Peter Mossey,Régine P.M. Steegers‐Theunissen,Jan Lindemans,(unknown),Michele Rubini,(unknown),Vincenzo Aiello,Borut Peterlin,Anne M. Molloy,Markus M. Nöthen,Michael Knapp,Kerstin U. Ludwig	19
18	Detection of Head-to-Tail DNA Sequences of Human Bocavirus in Clinical Samples 2011 ·PLoS ONE ·Jessica Lüsebrink,Verena Schildgen,Ramona Liza Tillmann,(unknown),Anne C. Böhmer,Andreas Müller,Oliver Schildgen	60
19	Das "Kremser Modell": Erfolgreiches Disease-Management zur Betreuung von Patienten mit Herzinsuffizienz 2011 ·Journal für Kardiologie (Krause & Pachernegg GmbH) ·Anne C. Böhmer,Manfred Wieser,(unknown),(unknown),G Kronik	4
20	Novel application for isothermal nucleic acid sequence-based amplification (NASBA) 2009 ·Journal of Virological Methods ·Anne C. Böhmer,Verena Schildgen,Jessica Lüsebrink,Susanne Ziegler,Ramona Liza Tillmann,Michael Kleines,Oliver Schildgen	28

About Anne C. Böhmer

Anne C. Böhmer is a scholar working on Genetics, Genetics and Gastroenterology, having authored 21 papers that have together received 536 indexed citations. Recurring topics across this work include Cleft Lip and Palate Research (12 papers), Craniofacial Disorders and Treatments (10 papers) and Congenital Ear and Nasal Anomalies (6 papers). The work is most often cited by research in Gastroenterology (89 citations), Genetics (285 citations) and Genetics (59 citations). Anne C. Böhmer has collaborated with scholars based in Germany, Netherlands and United Kingdom. Frequent co-authors include Kerstin U. Ludwig, Elisabeth Mangold, Johannes Schumacher, Michael Knapp, Oliver Schildgen, Jessica Lüsebrink, Verena Schildgen, Ramona Liza Tillmann, Markus M. Nöthen and Andreas Müller. Their work appears in journals such as PLoS ONE, Gut and Human Molecular 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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