Jorieke E. H. Bergman

4.0k citations

51 papers · 1.6k indexed · h-index 22

Genetics top 1%
Pulmonary and Respiratory Medicine top 5%
Molecular Biology
Surgery top 10%
Genetics top 5%

Co-authors: Conny M.A. van Ravenswaaij‐Arts Lies H. Hoefsloot Robert M.W. Hofstra Hermien E. K. de Walle Marjolijn C.J. Jongmans Marian K. Bakker Lisbeth Tranebjærg Nicole Janssen
Topics: Tracheal and airway disorders (13 papers)Congenital Ear and Nasal Anomalies (13 papers)Congenital Anomalies and Fetal Surgery (11 papers)
Cited by: Genetics Developmental Biology Pulmonary and Respiratory Medicine
Journals: PLoS ONE The Journal of Clinical Endocrinology & Metabolism International Journal of Molecular Sciences
Partner nations: Netherlands United Kingdom Denmark

In The Last Decade

Jorieke E. H. Bergman

49 papers receiving 1.5k citations

Peers

Countries citing papers authored by Jorieke E. H. Bergman

Since Specialization

Citations

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

Fields of papers citing papers by Jorieke E. H. Bergman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jorieke E. H. Bergman. 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 Jorieke E. H. Bergman. The network helps show where Jorieke E. H. Bergman may publish in the future.

Co-authorship network of co-authors of Jorieke E. H. Bergman

This figure shows the co-authorship network connecting the top 25 collaborators of Jorieke E. H. Bergman. A scholar is included among the top collaborators of Jorieke E. H. Bergman 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 Jorieke E. H. Bergman. Jorieke E. H. Bergman 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	Updated EUROCAT guidelines for classification of cases with congenital anomalies 2024 ·Birth Defects Research ·Jorieke E. H. Bergman,(unknown),Ingeborg Barišić,Agnieszka Kinsner‐Ovaskainen,Joan K. Morris,David Tucker,Diana Wellesley,Ester Garne	8
2	Maternal first trimester COVID‐19 vaccination and risk of major non‐genetic congenital anomalies 2023 ·Birth Defects Research ·Petra J. Woestenberg,(unknown),Jorieke E. H. Bergman,(unknown),(unknown),A. Kant	5
3	A comparison of infants' birth defects self‐reported by mothers with data provided by general practitioners: Data from the Dutch Pregnancy Drug Register 2023 ·Birth Defects Research ·(unknown),(unknown),(unknown),Petra J. Woestenberg,Jorieke E. H. Bergman,(unknown)	0
4	Macrolide and lincosamide antibiotic exposure in the first trimester of pregnancy and risk of congenital anomaly: A European case-control study 2021 ·Reproductive Toxicology ·(unknown),Helen Dolk,Maria Loane,Karen Casson,Vera Nelen,Ingeborg Barišić,Ester Garne,(unknown),Mary O’Mahony,Amanda J. Neville,Anna Pierini,Jorieke E. H. Bergman,Kari Klungsøyr,Anna Materna‐Kiryluk,(unknown),Clara Cavero‐Carbonell,Marie-Claude Addor,David Tucker	12
5	Maternal occupational exposure to solvents and gastroschisis in offspring - National Birth Defects Prevention Study 1997–2011 2020 ·Occupational and Environmental Medicine ·(unknown),Lynn M. Almli,Tania A. Desrosiers,Kathryn E. Arnold,Jorieke E. H. Bergman,Hans Kromhout,H. Marike Boezen,Hermien E. K. de Walle,Carissa M. Rocheleau,Jennita Reefhuis	3
6	Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study 2019 ·BMJ Open ·Marian K. Bakker,Jorieke E. H. Bergman,Sergey Krikov,Emmanuelle Amar,Guido Cocchi,Janet D. Cragan,Hermien E. K. de Walle,Miriam Gatt,Boris Groisman,Shiliang Liu,Wendy N. Nembhard,Anna Pierini,Anke Rißmann,Shanthi Chidambarathanu,(unknown),Elena Szabová,Giovanna Tagliabue,David Tucker,Pierpaolo Mastroiacovo,Lorenzo D. Botto	140
7	Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe 2018 ·European Journal of Medical Genetics ·Ingeborg Barišić,(unknown),(unknown),Jorieke E. H. Bergman,Clara Cavero‐Carbonell,(unknown),Anna Materna‐Kiryluk,Anna Latos‐Bieleńska,Hanitra Randrianaivo,Natalya Zymak‐Zakutnya,(unknown),Monica Lanzoni,Joan K. Morris	22
8	Imaging of Clival Hypoplasia in CHARGE Syndrome and Hypothesis for Development: A Case-Control Study 2018 ·American Journal of Neuroradiology ·(unknown),Jorieke E. H. Bergman,Conny M.A. van Ravenswaaij‐Arts,Linda C. Meiners	9
9	Maternal use of drug substrates of placental transporters and the effect of transporter-mediated drug interactions on the risk of congenital anomalies 2017 ·PLoS ONE ·Nur Aizati Athirah Daud,Jorieke E. H. Bergman,(unknown),Wilhelmina S. Kerstjens‐Frederikse,Henk Groen,Jens Bos,Eelko Hak,Bob Wilffert	18
10	Congenital anomalies in offspring of subfertile couples: a registry-based study in the northern Netherlands 2015 ·Fertility and Sterility ·Jorien Seggers,Hermien E. K. de Walle,Jorieke E. H. Bergman,Henk Groen,Mijna Hadders‐Algra,(unknown),Annemieke Hoek,M.L. Haadsma	32
11	Folic acid supplementation influences the distribution of neural tube defect subtypes: A registry-based study 2015 ·Reproductive Toxicology ·Jorieke E. H. Bergman,Egbert Otten,Joanne Verheij,Hermien E. K. de Walle	11
12	Meckel–Gruber Syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in Europe 2014 ·European Journal of Human Genetics ·Ingeborg Barišić,(unknown),Maria Loane,Ester Garne,Diana Wellesley,Elisa Calzolari,Helen Dolk,Marie‐Claude Addor,Jorieke E. H. Bergman,Paula Braz,Elizabeth S. Draper,Martin Haeusler,Babak Khoshnood,Kari Klungsøyr,Anna Pierini,Annette Queißer‐Luft,Judith Rankin,Anke Rißmann,Christine Verellen‐Dumoulin	46
13	Birth prevalence for congenital limb defects in the northern Netherlands: a 30-year population-based study 2013 ·BMC Musculoskeletal Disorders ·(unknown),Corry K. van der Sluis,Anthonie J. van Essen,Jorieke E. H. Bergman,Pieter U. Dijkstra,Heleen A. Reinders‐Messelink,Hermien E. K. de Walle	63
14	A novel classification system to predict the pathogenic effects of CHD7 missense variants in CHARGE syndrome 2012 ·Human Mutation ·Jorieke E. H. Bergman,Nicole Janssen,Almer M. van der Sloot,Hermien E. K. de Walle,Jeroen Schoots,Nanna Dahl Rendtorff,Lisbeth Tranebjærg,Lies H. Hoefsloot,Conny M.A. van Ravenswaaij‐Arts,Robert M.W. Hofstra	50
15	The Results ofCHD7Analysis in Clinically Well-Characterized Patients with Kallmann Syndrome 2012 ·The Journal of Clinical Endocrinology & Metabolism ·Jorieke E. H. Bergman,Willem de Ronde,Marjolijn C.J. Jongmans,Bruce H. R. Wolffenbuttel,S L S Drop,Ad R. Hermus,Gianni Bocca,Lies H. Hoefsloot,Conny M.A. van Ravenswaaij‐Arts	44
16	CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype 2011 ·Journal of Medical Genetics ·Jorieke E. H. Bergman,(unknown),Lies H. Hoefsloot,Marjolijn C.J. Jongmans,Robert M.W. Hofstra,Conny M.A. van Ravenswaaij‐Arts	200
17	CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome 2010 ·Human Molecular Genetics ·(unknown),Lindsey M. Pieper,(unknown),(unknown),Sigrid Hoyer‐Fender,Miriam Elbracht,Jorieke E. H. Bergman,Lies H. Hoefsloot,Silke Pauli	57
18	Anosmia Predicts Hypogonadotropic Hypogonadism in CHARGE Syndrome 2010 ·The Journal of Pediatrics ·Jorieke E. H. Bergman,Gianni Bocca,Lies H. Hoefsloot,Linda C. Meiners,Conny M.A. van Ravenswaaij‐Arts	31
19	The many faces of aggressive aortic pathology: Loeys-Dietz syndrome 2008 ·Netherlands Heart Journal ·Jan J.J. Aalberts,Maarten P. van den Berg,Jorieke E. H. Bergman,Gideon J. du Marchie Sarvaas,Jan G. Post,(unknown),Gerard Pals,Piet W. Boonstra,J. Peter van Tintelen	30
20	Exon copy number alterations of the CHD7 gene are not a major cause of CHARGE and CHARGE-like syndrome 2008 ·European Journal of Medical Genetics ·Jorieke E. H. Bergman,(unknown),Marjolijn C.J. Jongmans,R.J.C. Admiraal,Lies H. Hoefsloot,Conny M.A. van Ravenswaaij‐Arts	26

About Jorieke E. H. Bergman

Jorieke E. H. Bergman is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Developmental Biology, having authored 51 papers that have together received 1.6k indexed citations. Recurring topics across this work include Tracheal and airway disorders (13 papers), Congenital Ear and Nasal Anomalies (13 papers) and Congenital Anomalies and Fetal Surgery (11 papers). The work is most often cited by research in Genetics (611 citations), Developmental Biology (53 citations) and Pulmonary and Respiratory Medicine (592 citations). Jorieke E. H. Bergman has collaborated with scholars based in Netherlands, United Kingdom and Denmark. Frequent co-authors include Conny M.A. van Ravenswaaij‐Arts, Lies H. Hoefsloot, Robert M.W. Hofstra, Hermien E. K. de Walle, Marjolijn C.J. Jongmans, Marian K. Bakker, Lisbeth Tranebjærg, Nicole Janssen, Jeroen Schoots and Marianne Lodahl. Their work appears in journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and International Journal of Molecular Sciences.

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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