D. J. J. Halley

1.9k citations

38 papers · 1.3k indexed · h-index 17

Co-authors: Martinus F. Niermeijer Ben A. Oostra Bert Ba de Vries Dick Lindhout J. O. Van Hemel H. Galjaard Senno Verhoef A.M.W. van den Ouweland
Topics: Tuberous Sclerosis Complex Research (10 papers)Genomic variations and chromosomal abnormalities (8 papers)Genetics and Neurodevelopmental Disorders (7 papers)
Cited by: Genetics Neurology Cognitive Neuroscience
Journals: Biochemical and Biophysical Research Communications Annals of the New York Academy of Sciences The American Journal of Human Genetics
Partner nations: Netherlands United States United Kingdom

In The Last Decade

D. J. J. Halley

38 papers receiving 1.2k citations

Peers

Countries citing papers authored by D. J. J. Halley

Since Specialization

Citations

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

Fields of papers citing papers by D. J. J. Halley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D. J. J. Halley

This figure shows the co-authorship network connecting the top 25 collaborators of D. J. J. Halley. A scholar is included among the top collaborators of D. J. J. Halley 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 D. J. J. Halley. D. J. J. Halley 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	High Rate of Mosaicism in Tuberous Sclerosis Complex 1999 ·The American Journal of Human Genetics ·Senno Verhoef,(unknown),(unknown),(unknown),Tadeusz Mazurczak,Sergiusz Jóźwiak,A. Fois,G. Bartalini,Bernard A. Zonnenberg,Anthonie J. van Essen,Dick Lindhout,D. J. J. Halley,Ans M.W. van den Ouweland	121
2	Malignant pancreatic tumour within the spectrum of tuberous sclerosis complex in childhood 1999 ·European Journal of Pediatrics ·Senno Verhoef,(unknown),W.L. Akkersdijk,N. M. A. Bax,Yavuz Ariyürek,Caroline Hermans,Onno van Nieuwenhuizen,(unknown),Dick Lindhout,D. J. J. Halley,(unknown),(unknown)	82
3	The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic data 1999 ·Human Reproduction ·Gert R. Dohle,(unknown),Shelley E. Overbeek,A.M.W. van den Ouweland,D. J. J. Halley,R. F. A. Weber,Martinus F. Niermeijer	39
4	The fragile X syndrome. 1998 ·Journal of Medical Genetics ·Bert Ba de Vries,D. J. J. Halley,Ben A. Oostra,Martinus F. Niermeijer	190
5	Deletions spanning the neurofibromatosis type 1 gene: Implications for genotype-phenotype correlations in neurofibromatosis type 1? 1997 ·Human Mutation ·Marjon H. Cnossen,(unknown),Martijn H. Breuning,Christi J. van Asperen,(unknown),Ans T. van der Ploeg,Arja de Goede-Bolder,(unknown),D. J. J. Halley,Martinus F. Niermeijer	92
6	A 1.7-Megabase Sequence-Ready Cosmid Contig Covering the TSC1 Candidate Region in 9q34 1997 ·Genomics ·Nick Hornigold,Marjon van Slegtenhorst,Joseph Nahmias,Rosemary Ekong,Sophie Rousseaux,Caroline Hermans,D. J. J. Halley,Sue Povey,Jonathan Wolfe	14
7	Cloning and evaluation of RALGDS as a candidate for the tuberous sclerosis gene TSC1 1997 ·Annals of Human Genetics ·(unknown),J. Kwiatkowska,Elizabeth P. Henske,J. L. Haines,D. J. J. Halley,Marjon van Slegtenhorst,D J Kwiatkowski	6
8	Angelman syndrome in an inbred family 1996 ·Human Genetics ·Joke Beuten,Raoul C. M. Hennekam,Bernadette Van Roy,Kathelijne Mangelschots,James S. Sutcliffe,D. J. J. Halley,Frederic A. M. Hennekam,Arthur L. Beaudet,Patrick J. Willems	3
9	Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndrome. 1996 ·Acta Biochimica Polonica ·Michał Milewski,(unknown),Jerzy Bal,Wout H. Deelen,Ewa Obersztyn,Ewa Bocian,D. J. J. Halley,J. Horst,Tadeusz Mazurczak	1
10	Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family. 1996 ·Journal of Medical Genetics ·(unknown),(unknown),Annelien Duits,(unknown),Rob Willemsen,J. O. Van Hemel,A M van den Ouweland,Martinus F. Niermeijer,B. A. Oostra,D. J. J. Halley	62
11	DNA diagnosis of Prader-Willi and Angelman syndromes with the probe PW71 (D15S63) 1995 ·Human Genetics ·(unknown),(unknown),Eveline Wesby–van Swaay,(unknown),Frans J. Los,J. O. Van Hemel,Raoul C. M. Hennekam,(unknown),Martinus F. Niermeijer,D. J. J. Halley	12
12	Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype. 1993 ·Journal of Medical Genetics ·Bert Ba de Vries,J. P. Fryns,Merlin G. Butler,(unknown),Eveline Wesby–van Swaay,J. O. Van Hemel,Ben A. Oostra,D. J. J. Halley,Martinus F. Niermeijer	73
13	In search for genes predisposing to epilepsy: Motives and methods 1992 ·Acta Neurologica Scandinavica ·Dick Lindhout,(unknown),D. J. J. Halley,Dorothée Kasteleijn‐Nolst Trenité	1
14	DNA analysis in patients with lissencephaly type I and other cortical dysplasias 1991 ·American Journal of Medical Genetics ·B. A. Oostra,J.F. de Rijk-van Andel,H. J. Eussen,J. O. Van Hemel,D. J. J. Halley,Martinus F. Niermeijer	5
15	Isolated lissencephaly sequence associated with a microdeletion at chromosome 17p13 1991 ·Human Genetics ·J.F. de Rijk-van Andel,Coriene E. Catsman‐Berrevoets,D. J. J. Halley,Eveline Wesby–van Swaay,Martinus F. Niermeijer,B. A. Oostra	5
16	An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two‐Point Methods^a 1991 ·Annals of the New York Academy of Sciences ·Sue Povey,(unknown),(unknown),Mari‐Wyn Burley,M. Smith,Pamela Flodman,N.E. Morton,J. H. Edwards,Julian R. Sampson,John R.W. Yates,J. L. Haines,J. Amos,M. Priscilla Short,L. A. Sandkuyl,D. J. J. Halley,Alan Fryer,(unknown),Rolf Mueller,(unknown),M Super,(unknown)	16
17	A Comparative Study on Genetic Heterogeneity in Tuberous Sclerosis: Evidence for One Gene on 9q34 and a Second Gene on 11q22–23^a 1991 ·Annals of the New York Academy of Sciences ·(unknown),Sue Povey,(unknown),L. A. Sandkuyl,Dick Lindhout,Pamela Flodman,M. Smith,Julian R. Sampson,(unknown),(unknown),P Fleury,Priscilla Short,J. Amos,D. J. J. Halley	22
18	New polymorphic DNA marker close to the fragile site FRAXA 1990 ·Genomics ·B. A. Oostra,(unknown),(unknown),Coen A. M. van Bennekom,Egbert Bakker,D. J. J. Halley,Malgorzata Schmidt,Desirée du Sart,Anne Smits,Bé Wieringa,Bernard A. van Oost	49
19	The mutation ΔF508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosis 1990 ·Human Genetics ·D. J. J. Halley,Henk J. Veeze,L. A. Sandkuyl,Eveline Wesby–van Swaay,(unknown),Wout H. Deelen,(unknown),M. F. Niermeijer	8
20	Cystic fibrosis: screening for a DNA deletion by field inversion gel electrophoresis 1988 ·Human Genetics ·J. Morreau,M. Sinaasappel,Ben A. Oostra,D. J. J. Halley	3

About D. J. J. Halley

D. J. J. Halley is a scholar working on Genetics, Physiology and Rheumatology, having authored 38 papers that have together received 1.3k indexed citations. Recurring topics across this work include Tuberous Sclerosis Complex Research (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (7 papers). The work is most often cited by research in Genetics (555 citations), Neurology (168 citations) and Cognitive Neuroscience (207 citations). D. J. J. Halley has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Martinus F. Niermeijer, Ben A. Oostra, Bert Ba de Vries, Dick Lindhout, J. O. Van Hemel, H. Galjaard, Senno Verhoef, A.M.W. van den Ouweland, Lodewijk A. Sandkuijl and Peter Heutink. Their work appears in journals such as Biochemical and Biophysical Research Communications, Annals of the New York 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.

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