Marja W. Wessels

6.5k citations

64 papers · 2.1k indexed · h-index 24

Molecular Biology top 10%
Genetics top 2%
Cardiology and Cardiovascular Medicine top 5%
Pulmonary and Respiratory Medicine top 5%
Epidemiology top 10%

Co-authors: Patrick J. Willems Martinus F. Niermeijer Nicolette S. den Hollander Ingrid M.E. Frohn-Mulder Yvonne M. Hoedemaekers Dennis Dooijes Ronald R. de Krijger Michelle Michels
Topics: Congenital heart defects research (13 papers)Connective tissue disorders research (11 papers)Cardiomyopathy and Myosin Studies (10 papers)
Cited by: Genetics Cardiology and Cardiovascular Medicine Immunology and Allergy
Journals: Science New England Journal of Medicine Circulation
Partner nations: Netherlands United States Belgium

In The Last Decade

Marja W. Wessels

60 papers receiving 2.1k citations

Peers

Countries citing papers authored by Marja W. Wessels

Since Specialization

Citations

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

Fields of papers citing papers by Marja W. Wessels

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marja W. Wessels. 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 Marja W. Wessels. The network helps show where Marja W. Wessels may publish in the future.

Co-authorship network of co-authors of Marja W. Wessels

This figure shows the co-authorship network connecting the top 25 collaborators of Marja W. Wessels. A scholar is included among the top collaborators of Marja W. Wessels 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 Marja W. Wessels. Marja W. Wessels 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	Phenotypic variability of filamin C–related cardiomyopathy: Insights from a novel Dutch founder variant 2023 ·Heart Rhythm ·(unknown),(unknown),Alexander Hirsch,Marjon A. van Slegtenhorst,Marja W. Wessels,Jan H. von der Thüsen,Annette F. Baas,(unknown),Job A.J. Verdonschot,Paul A. van der Zwaag,Judith M.A. Verhagen,Michelle Michels	1
2	Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort 2022 ·Genetics in Medicine ·(unknown),Judith M.A. Verhagen,Jos A. Bekkers,Marlies Kempers,Arjan C. Houweling,Marieke J.H. Baars,Eline Overwater,Yvonne Hilhorst‐Hofstee,Daniela Q.C.M. Barge‐Schaapveld,(unknown),Ingrid P.C. Krapels,(unknown),Marja W. Wessels,Bart Loeys,Hence J.M. Verhagen,Alessandra Maugeri,Jolien W. Roos‐Hesselink,Hennie T. Brüggenwirth,Ingrid M.B.H. van de Laar	3
3	Blood biomarkers in patients with bicuspid aortic valve disease 2020 ·Journal of Cardiology ·Lidia R. Bons,Laurie W. Geenen,Allard T. van den Hoven,Willem A. Dik,Annemien E. van den Bosch,Anthonie L. Duijnhouwer,Hans‐Marc J. Siebelink,Ricardo P.J. Budde,Eric Boersma,Marja W. Wessels,Ingrid M.B.H. van de Laar,Marco C. DeRuiter,Marie‐José Goumans,Bart Loeys,Jolien W. Roos‐Hesselink	4
4	Cardiac Phenotypes, Genetics, and Risks in Familial Noncompaction Cardiomyopathy 2019 ·Journal of the American College of Cardiology ·Jaap I. van Waning,Kadir Çalişkan,Michelle Michels,Arend F. L. Schinkel,Alexander Hirsch,Michiel Dalinghaus,Yvonne M. Hoedemaekers,Marja W. Wessels,Arne IJpma,Robert M.W. Hofstra,Marjon A. van Slegtenhorst,Daniëlle Majoor‐Krakauer	45
5	Expert consensus recommendations on the cardiogenetic care for patients with thoracic aortic disease and their first-degree relatives 2018 ·International Journal of Cardiology ·Judith M.A. Verhagen,Marlies Kempers,Luc Cozijnsen,Berto J. Bouma,Anthonie L. Duijnhouwer,Jan G. Post,Yvonne Hilhorst‐Hofstee,Sebastiaan C.A.M. Bekkers,Wilhelmina S. Kerstjens‐Frederikse,Thomas J. van Brakel,(unknown),Marja W. Wessels,Bart Loeys,Jolien W. Roos‐Hesselink,Ingrid M.B.H. van de Laar	40
6	Lack of evidence for a causal role of CALR3 in monogenic cardiomyopathy 2018 ·European Journal of Human Genetics ·Judith M.A. Verhagen,(unknown),Paul A. van der Zwaag,Jan H. von der Thüsen,Erwin Brosens,Imke Christiaans,Dennis Dooijes,(unknown),Ronald H. Lekanne Deprez,Michelle Michels,Anneke M. van Mil,Rogier A. Oldenburg,Jasper J. van der Smagt,Arthur van den Wijngaard,Marja W. Wessels,Robert M.W. Hofstra,Marjon A. van Slegtenhorst,Jan D.H. Jongbloed,Ingrid M.B.H. van de Laar	5
7	Rodriguez acrofacial dysostosis is caused by apparently de novo heterozygous mutations in the SF3B4 gene 2016 ·American Journal of Medical Genetics Part A ·Melita Irving,Boyan Dimitrov,Marja W. Wessels,Muriel Holder‐Espinasse,David Chitayat,Michael A. Simpson	12
8	Phenotypic Variability Associated with a Large Recurrent 1q21.1 Microduplication in a Three-Generation Family 2015 ·Molecular Syndromology ·Judith M.A. Verhagen,Nicole de Leeuw,Dimitri N.M. Papatsonis,E. W. M. Grijseels,Ronald R. de Krijger,Marja W. Wessels	17
9	Incomplete segregation of MYH11 variants with thoracic aortic aneurysms and dissections and patent ductus arteriosus 2012 ·European Journal of Human Genetics ·Magdaléna Harakaľová,Jasper van der Smagt,Carolien G. F. de Kovel,Ruben van’t Slot,Martin Poot,Isaäc J. Nijman,Jelena Medic,(unknown),Jaap W. Deckers,Jolien W. Roos‐Hesselink,Marja W. Wessels,Hubert F. Baars,Marjan M. Weiss,Gerard Pals,Lisa Golmard,Xavier Jeunemaı̂tre,Dick Lindhout,Edwin Cuppen,Annette F. Baas	32
10	Phenotypic variability of atypical 22q11.2 deletions not includingTBX1 2012 ·American Journal of Medical Genetics Part A ·Judith M.A. Verhagen,Karin E. M. Diderich,Grétel Oudesluijs,Grazia M.S. Mancini,Alex J. Eggink,Anna C. Verkleij‐Hagoort,Irene A.L. Groenenberg,Patrick J. Willems,(unknown),de Man,Malgorzata I. Srebniak,Diane Van Opstal,Lorette O. M. Hulsman,Laura J. C. M. van Zutven,Marja W. Wessels	42
11	Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome 2012 ·Nature Genetics ·Gijs W.E. Santen,Emmelien Aten,Yu Sun,Rowida Almomani,Christian Gilissen,Maartje Nielsen,Sarina G. Kant,I. Snoeck,E Peeters,Yvonne Hilhorst‐Hofstee,Marja W. Wessels,Nicolette S. den Hollander,Claudia Ruivenkamp,Gert‐Jan B. van Ommen,Martijn H. Breuning,Johan T. den Dunnen,Arie van Haeringen,Marjolein Kriek	235
12	Identification of RNA binding motif proteins essential for cardiovascular development 2011 ·BMC Developmental Biology ·Samantha Maragh,Ronald Miller,Seneca L. Bessling,David McGaughey,Marja W. Wessels,(unknown),Eric A. Stone,Aida M. Bertoli‐Avella,John D. Gearhart,Shannon Fisher,Andrew S. McCallion	23
13	Functional characterisation of the TSC1–TSC2 complex to assess multiple TSC2 variants identified in single families affected by tuberous sclerosis complex 2008 ·BMC Medical Genetics ·Mark Nellist,Őzgür Sancak,Miriam Goedbloed,(unknown),Marja W. Wessels,(unknown),Marieke J.H. Baars,Charlotte J. Dommering,(unknown),Dicky Halley	16
14	Mutations in sarcomeric protein genes not only lead to cardiomyopathy but also to congenital cardiovascular malformations 2008 ·Clinical Genetics ·Marja W. Wessels,Patrick J. Willems	11
15	Three new families with arterial tortuosity syndrome 2004 ·American Journal of Medical Genetics Part A ·Marja W. Wessels,Coriene E. Catsman‐Berrevoets,Grazia M.S. Mancini,Martijn H. Breuning,(unknown),Hans Stroink,(unknown),Paul Coucke,Anne De Paepe,Martinus F. Niermeijer,Patrick J. Willems	57
16	Prenatal diagnosis of boomerang dysplasia 2003 ·American Journal of Medical Genetics Part A ·Marja W. Wessels,Nicolette S. den Hollander,Ronald R. de Krijger,(unknown),Andrea Superti‐Furga,Peter G. J. Nikkels,Patrick J. Willems	4
17	Fetus with an unusual form of nonrhizomelic chondrodysplasia punctata: Case report and review 2003 ·American Journal of Medical Genetics Part A ·Marja W. Wessels,(unknown),Ronald R. de Krijger,Peter G. J. Nikkels,Helen Brandenburg,Raoul C. M. Hennekam,Patrick J. Willems	12
18	Kabuki syndrome: a review study of three hundred patients 2002 ·Clinical Dysmorphology ·Marja W. Wessels,Alice S. Brooks,Jeannette Hoogeboom,Martinus F. Niermeijer,Patrick J. Willems	83
19	Congenital microcephaly detected by prenatal ultrasound: genetic aspects and clinical significance 2000 ·Ultrasound in Obstetrics and Gynecology ·Nicolette S. den Hollander,Marja W. Wessels,Frans J. Los,N. T. C. Ursem,Martinus F. Niermeijer,J. W. Wladimiroff	26
20	IgE antibodies to Pityrosporum ovale in atopic dermatitis 1991 ·British Journal of Dermatology ·Marja W. Wessels,(unknown),Adrie G. van Ieperen-van Dijk,(unknown),E. YOUNG	79

About Marja W. Wessels

Marja W. Wessels is a scholar working on Genetics, Developmental Neuroscience and Cardiology and Cardiovascular Medicine, having authored 64 papers that have together received 2.1k indexed citations. Recurring topics across this work include Congenital heart defects research (13 papers), Connective tissue disorders research (11 papers) and Cardiomyopathy and Myosin Studies (10 papers). The work is most often cited by research in Genetics (735 citations), Cardiology and Cardiovascular Medicine (467 citations) and Immunology and Allergy (96 citations). Marja W. Wessels has collaborated with scholars based in Netherlands, United States and Belgium. Frequent co-authors include Patrick J. Willems, Martinus F. Niermeijer, Nicolette S. den Hollander, Ingrid M.E. Frohn-Mulder, Yvonne M. Hoedemaekers, Dennis Dooijes, Ronald R. de Krijger, Michelle Michels, Paul Coucke and Alice S. Brooks. Their work appears in journals such as Science, New England Journal of Medicine and Circulation.

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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