Bert van der Zwaag

4.6k citations

44 papers · 2.2k indexed · 1 hit paper · h-index 23

Molecular Biology top 10%
Genetics top 5%
Cellular and Molecular Neuroscience top 5%
Cell Biology top 5%
Surgery

Co-authors: J. Peter H. Burbach George W. Padberg Hans van Bokhoven Han G. Brunner H. T. F. M. Verzijl J.R.M. Cruysberg Christopher A. Walsh Bru Cormand
Topics: Genomic variations and chromosomal abnormalities (7 papers)Genomics and Rare Diseases (6 papers)Renal Diseases and Glomerulopathies (6 papers)
Cited by: Genetics Sensory Systems Cellular and Molecular Neuroscience
Journals: Journal of Clinical Investigation PLoS ONE Neurology
Partner nations: Netherlands United States Germany

In The Last Decade

Bert van der Zwaag

42 papers receiving 2.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in the O-Mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndrome

2002 519 citations Sophie Currier, Alice Steinbrecher et al. The American Journal of Human Genetics profile →

Peers

Countries citing papers authored by Bert van der Zwaag

Since Specialization

Citations

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

Fields of papers citing papers by Bert van der Zwaag

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bert van der Zwaag. 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 Bert van der Zwaag. The network helps show where Bert van der Zwaag may publish in the future.

Co-authorship network of co-authors of Bert van der Zwaag

This figure shows the co-authorship network connecting the top 25 collaborators of Bert van der Zwaag. A scholar is included among the top collaborators of Bert van der Zwaag 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 Bert van der Zwaag. Bert van der Zwaag 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	Medullary Sponge Kidney and Its Relationship with Primary Distal Renal Tubular Acidosis: Case Reports and a Comprehensive Genetics-First Approach 2024 ·The Nephron journals/Nephron journals ·Gerrit van den Berg,(unknown),Bert van der Zwaag,Phillis Lakeman,Lotte Kaasenbrood,John A. Sayer,Marc R. Liliën,Albertien M. van Eerde	1
2	The Importance of Copy Number Variant Analysis in Patients with Monogenic Kidney Disease 2024 ·Kidney International Reports ·(unknown),Robert F. Ernst,Martin Elferink,Hanneke W. M. van Deutekom,Bert van der Zwaag,Albertien M. van Eerde	0
3	Clinical Characterization of a National Cohort of Patients With Germline WT1 Variants Including Late-Onset Phenotypes 2024 ·Kidney International Reports ·(unknown),Roland P. Kuiper,Janna A. Hol,(unknown),Bert van der Zwaag,Marc R. Liliën,Maria Lombardi,Marry M. van den Heuvel‐Eibrink,Marjolijn C.J. Jongmans	0
4	Diagnostic yield of massively parallel sequencing in patients with chronic kidney disease of unknown etiology: rationale and design of a national prospective cohort study 2022 ·BMJ Open ·(unknown),Mark Eijgelsheim,Liffert Vogt,Bert van der Zwaag,Albertien M. van Eerde,Nine V.A.M. Knoers,Martin H. de Borst	5
5	Identifying underlying medical causes of pediatric obesity: Results of a systematic diagnostic approach in a pediatric obesity center 2020 ·PLoS ONE ·Lotte Kleinendorst,Ozair Abawi,Bibian van der Voorn,(unknown),(unknown),Jenny A. Visser,Elisabeth F. C. van Rossum,Bert van der Zwaag,Mariëlle Alders,Elles M. J. Boon,Mieke M. van Haelst,Erica L T van den Akker	42
6	Association of Cell Adhesion Molecules Contactin-6 and Latrophilin-1 Regulates Neuronal Apoptosis 2016 ·Frontiers in Molecular Neuroscience ·Amila Zuko,Asami Oguro‐Ando,Harm Post,(unknown),Roland E. van Dijk,Maarten Altelaar,Albert J. R. Heck,Alexander G. Petrenko,Bert van der Zwaag,Yasushi Shimoda,R. Jeroen Pasterkamp,J. Peter H. Burbach	24
7	Joubert syndrome: genotyping a Northern European patient cohort 2015 ·European Journal of Human Genetics ·Hester Y. Kroes,Glen R. Monroe,Bert van der Zwaag,Karen Duran,Carolien G. F. de Kovel,(unknown),Magdaléna Harakaľová,Isaäc J. Nijman,Wigard P. Kloosterman,Rachel H. Giles,Nine Knoers,Gijs van Haaften	50
8	Targeted next-generation sequencing: A novel diagnostic tool for primary immunodeficiencies 2013 ·Journal of Allergy and Clinical Immunology ·Isaäc J. Nijman,Joris M. van Montfrans,Marlous Hoogstraat,Marianne Boes,Lisette van de Corput,Ellen D. Renner,(unknown),Stef van Lieshout,Martin Elferink,Mirjam van der Burg,Clementien L. Vermont,Bert van der Zwaag,Esther Janson,Edwin Cuppen,Johannes Kristian Ploos van Amstel,Mariëlle van Gijn	95
9	Contactins in the neurobiology of autism 2013 ·European Journal of Pharmacology ·Amila Zuko,(unknown),Asami Oguro‐Ando,Martien J. Kas,Emma van Daalen,Bert van der Zwaag,J. Peter H. Burbach	75
10	The transcription factor Uncx4.1 acts in a short window of midbrain dopaminergic neuron differentiation 2012 ·Neural Development ·(unknown),(unknown),(unknown),Andreas Kispert,Michael Leitges,Bert van der Zwaag,J. Peter H. Burbach,Frédérique Varoqueaux,Ahmed Mansouri	12
11	The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitotically 2012 ·PubMed ·Ferry F.J. Kersten,Erwin van Wijk,Lisette Hetterschijt,(unknown),Theo Peters,Mariam G. Aslanyan,Bert van der Zwaag,Uwe Wolfrum,Jan E.E. Keunen,Ronald Roepman,Hannie Kremer	14
12	Gain of glycosylation in integrin α3 causes lung disease and nephrotic syndrome 2012 ·Journal of Clinical Investigation ·Nayia Nicolaou,Coert Margadant,Sietske H. Kevelam,Marc R. Liliën,Michiel J.S. Oosterveld,Maaike Kreft,Albertien M. van Eerde,Rolph Pfundt,Pauline Terhal,Bert van der Zwaag,Peter G. J. Nikkels,Norman Sachs,Roel Goldschmeding,Nine V.A.M. Knoers,Kirsten Y. Renkema,Arnoud Sonnenberg	96
13	A patient with a mild holoprosencephaly spectrum phenotype and heterotaxy and a 1.3 Mb deletion encompassing GLI2 2011 ·American Journal of Medical Genetics Part A ·Sietske H. Kevelam,J. J. T. van Harssel,Bert van der Zwaag,H.J.M. Smeets,Aimée Paulussen,Klaske D. Lichtenbelt	25
14	Contactins 2011 ·Advances in protein chemistry and structural biology ·Amila Zuko,Samuel Bouyain,Bert van der Zwaag,J. Peter H. Burbach	42
15	A co‐segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder 2009 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Bert van der Zwaag,Wouter Staal,Ron Hochstenbach,Martin Poot,Henk A. Spierenburg,Maretha Jonge,Nienke E. Verbeek,Ruben van ‘t Slot,Michael A. van Es,Frank J. T. Staal,Christine M. Freitag,Jacobine E. Buizer‐Voskamp,Marcel Nelen,Leonard H. van den Berg,Hans Kristian Ploos van Amstel,Hermán van Engeland,J. Peter H. Burbach	80
16	Contact in the genetics of autism and schizophrenia 2009 ·Trends in Neurosciences ·J. Peter H. Burbach,Bert van der Zwaag	122
17	Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen 2008 ·The Lancet Neurology ·Hylke M. Blauw,Jan H. Veldink,Michael A. van Es,(unknown),Christiaan G. J. Saris,Bert van der Zwaag,Lude Franke,J. Peter H. Burbach,John H. J. Wokke,Roel A. Ophoff,Leonard H. van den Berg	74
18	Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresis 2005 ·Developmental Brain Research ·Bert van der Zwaag,J. Peter H. Burbach,Han G. Brunner,Hans van Bokhoven,George W. Padberg	3
19	Identifying new candidate genes for hereditary facial paresis on chromosome 3q21–q22 by RNA in situ hybridization in mouse 2005 ·Genomics ·Bert van der Zwaag,J. Peter H. Burbach,Curt Scharfe,Peter J. Oefner,Han G. Brunner,George W. Padberg,Hans van Bokhoven	16
20	Mutations in the O-Mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndromebreakdown → 2002 ·The American Journal of Human Genetics ·(unknown),Sophie Currier,Alice Steinbrecher,Jacopo Celli,Ellen van Beusekom,Bert van der Zwaag,Hülya Kayserili,Luciano Merlini,David Chitayat,William B. Dobyns,Bru Cormand,(unknown),Jesús Cruces,Thomas Voït,Christopher A. Walsh,Hans van Bokhoven,Han G. Brunner	519

About Bert van der Zwaag

Bert van der Zwaag is a scholar working on Nephrology, Immunology and Allergy and Genetics, having authored 44 papers that have together received 2.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers) and Renal Diseases and Glomerulopathies (6 papers). The work is most often cited by research in Genetics (704 citations), Sensory Systems (105 citations) and Cellular and Molecular Neuroscience (372 citations). Bert van der Zwaag has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include J. Peter H. Burbach, George W. Padberg, Hans van Bokhoven, Han G. Brunner, H. T. F. M. Verzijl, J.R.M. Cruysberg, Christopher A. Walsh, Bru Cormand, Jacopo Celli and Alice Steinbrecher. Their work appears in journals such as Journal of Clinical Investigation, PLoS ONE and Neurology.

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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