P J Willems

1.9k citations

36 papers · 1.3k indexed · h-index 17

Co-authors: Guy Van Camp Richard J. Smith Wim Van Hul Paul Coucke Jean‐Jacques Martin Wendy Balemans Joris Verlooy Erna Dams
Topics: Hearing, Cochlea, Tinnitus, Genetics (9 papers)Genetics and Neurodevelopmental Disorders (6 papers)Vestibular and auditory disorders (4 papers)
Cited by: Sensory Systems Otorhinolaryngology Neurology
Journals: New England Journal of Medicine Proceedings of the National Academy of Sciences The American Journal of Human Genetics
Partner nations: Belgium Netherlands United States

In The Last Decade

P J Willems

36 papers receiving 1.3k citations

Peers

Countries citing papers authored by P J Willems

Since Specialization

Citations

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

Fields of papers citing papers by P J Willems

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P J Willems. 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 P J Willems. The network helps show where P J Willems may publish in the future.

Co-authorship network of co-authors of P J Willems

This figure shows the co-authorship network connecting the top 25 collaborators of P J Willems. A scholar is included among the top collaborators of P J Willems 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 P J Willems. P J Willems is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Severe Developmental Delay in a Patient with 7p21.1–p14.3 Microdeletion Spanning the <i>TWIST</i> Gene and the <i>HOXA</i> Gene Cluster 2011 ·Molecular Syndromology ·Helen Fryssira,Periklis Makrythanasis,Antonis Kattamis,(unknown),Björn Menten,Kenjiro Kosaki,P J Willems,Emmanuel Kanavakis	14
2	Three Novel Mutations in Greek Sotos Patients with Rare Clinical Manifestations 2008 ·Hormone Research in Paediatrics ·Georgios Leventopoulos,Sophia Kitsiou‐Tzeli,Stavroula Psoni,Ariadni Mavrou,Emmanuel Kanavakis,P J Willems,Helen Fryssira	5
3	Clinical Presentation of DFNA8-DFNA12 2002 ·Advances in oto-rhino-laryngology ·Paul Govaerts,(unknown),Kristin Daemers,K. Verhoeven,Guy Van Camp,Isabelle Schatteman,Margriet Verstreken,P J Willems,Thomas Somers,F.E. Offeciers	3
4	Genetic Causes of Hearing Loss 2000 ·New England Journal of Medicine ·P J Willems	141
5	Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome 1999 ·Journal of Medical Genetics ·Paul Coucke,Peter Van Hauwe,Lorraine A. Everett,Osman Demırhan,(unknown),Nicole Dietrich,Richard J. Smith,Beth Coyle,William Reardon,Richard C. Trembath,P J Willems,(unknown),Guy Van Camp	40
6	A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2). 1998 ·Journal of Medical Genetics ·Nicholas Lench,Alex Markham,R Mueller,David P. Kelsell,Richard J. Smith,P J Willems,Isabelle Schatteman,(unknown),Paul Van de Heyning,Guy Van Camp	29
7	Nonsyndromic Autosomal Dominant Progressive Sensorineural Hearing Loss: Audiologic Analysis of a Pedigree Linked to DFNA2 1998 ·The Laryngoscope ·Henricus P. M. Kunst,Henri A. M. Marres,P.L.M. Huygen,(unknown),Guy Van Camp,Peter Van Hauwe,Paul Coucke,P J Willems,Cor W. R. J. Cremers	21
8	Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses 1998 ·The American Journal of Human Genetics ·Wim Wuyts,Wim Van Hul,Kristel De Boulle,Jan Hendrickx,Egbert Bakker,Filip Vanhoenacker,(unknown),Hermann‐Josef Lüdecke,Bekir Sıtkı Şaylı,Ugo E. Pazzaglia,Geert Mortier,B Hamel,(unknown),Mark Matsushita,(unknown),P J Willems	155
9	Inherited Nonsyndromic Hearing Loss: An Audiovestibular Study in a Large Family With Autosomal Dominant Progressive Hearing Loss Related to DFNA2 1997 ·Archives of Otolaryngology - Head and Neck Surgery ·Henri A. M. Marres,(unknown),P.L.M. Huygen,Henricus P. M. Kunst,Guy Van Camp,Paul Coucke,P J Willems,Cor W. R. J. Cremers	35
10	Assignment of the human Integral TransMembrane protein 1 gene (ITM1) to human chromosome band 11 q23.3 by in situ hybridization and YAC mapping 1996 ·Cytogenetic and Genome Research ·Wim Van Hul,(unknown),J. Wauters,Els Van Hul,N. Nowak,T.B. Shows,P J Willems,J. Merregaert	2
11	Retarded and Aberrant Splicings Caused by Single Exon Mutation in a Phosphoglycerate Kinase Variant 1996 ·Archives of Biochemistry and Biophysics ·Tomomi Ookawara,Vibha Davé,P J Willems,Jean‐Jacques Martin,Thierry de Barsy,E Matthys,A Yoshida	27
12	Instability of microsatellites in human gliomas. 1995 ·PubMed ·Erna Dams,(unknown),Jean‐Jacques Martin,Joris Verlooy,P J Willems	62
13	Characterization of FMR1 proteins isolated from different tissues 1995 ·Human Molecular Genetics ·(unknown),Esther de Graaff,C.E. Bakker,Rob Willemsen,P J Willems,(unknown),H. Galjaard,Arnold Reuser,B. A. Oostra,A. T. Hoogeveen	67
14	Tricho‐rhino‐phalangeal syndrome type I (TRP I) due to an apparently balanced translocation involving 8q24 1993 ·American Journal of Medical Genetics ·(unknown),(unknown),Paul M. Parizel,Julien Lambert,(unknown),Jules G. Leroy,(unknown),P J Willems,Jan E. Dumon	7
15	Localization of a Gene Responsible for Nonspecific Mental Retardation (MRX9) to the Pericentromeric Region of the X Chromosome 1993 ·Genomics ·P J Willems,Lieve Vits,Inge Buntinx,Peter Raeymaekers,Christine Van Broeckhoven,Berten Ceulemans	15
16	An EcoRI RFLP in the 5′ region of the human NF1 gene 1993 ·Human Genetics ·Edwin Reyniers,Kristel De Boulle,Douglas A. Marchuk,Lone B. Andersen,Francis S. Collins,P J Willems	7
17	Further evidence for dominant inheritance at the chromosome 15q11‐13 locus in familial angelman syndrome 1992 ·American Journal of Medical Genetics ·Jill Clayton‐Smith,T. Webb,S. Robb,(unknown),P J Willems,Stephen T.S. Lam,(unknown),M Pembrey,S Malcolm	29
18	Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22 1991 ·Genomics ·P J Willems,Jan Hendrickx,Bart Van Der Auwera,Lieve Vits,Peter Raeymaekers,Paul Coucke,(unknown),Ruud Berger,Gerrit Smit,Christine Van Broeckhoven,Manfred W. Kilimann,(unknown),John Fernandes	16
19	DNA Diagnosis of Cystic Fibrosis by Direct Detection of the Af508 Mutation 1991 ·Acta Clinica Belgica ·Jan Hendrickx,J. Wauters,Paul Coucke,Lieve Vits,Bart Van Der Auwera,P J Willems	1
20	Partial lyonisation of steroid sulphatase gene in single hair roots 1985 ·Journal of Inherited Metabolic Disease ·P J Willems,H.W.A. de Bruijn,(unknown),(unknown),Rolf M.F. Berger	5

About P J Willems

P J Willems is a scholar working on Sensory Systems, Genetics and Neurology, having authored 36 papers that have together received 1.3k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (9 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Vestibular and auditory disorders (4 papers). The work is most often cited by research in Sensory Systems (559 citations), Otorhinolaryngology (141 citations) and Neurology (264 citations). P J Willems has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Guy Van Camp, Richard J. Smith, Wim Van Hul, Paul Coucke, Jean‐Jacques Martin, Wendy Balemans, Joris Verlooy, Erna Dams, Neva E. Haites and Stuart H. Ralston. Their work appears in journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The American Journal of Human 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.

Explore authors with similar magnitude of impact