D. J. J. Halley

1.9k total citations
38 papers, 1.3k citations indexed

About

D. J. J. Halley is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, D. J. J. Halley has authored 38 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 15 papers in Molecular Biology and 13 papers in Physiology. Recurrent topics in D. J. J. Halley's work include Tuberous Sclerosis Complex Research (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (7 papers). D. J. J. Halley is often cited by papers focused on Tuberous Sclerosis Complex Research (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (7 papers). D. J. J. Halley collaborates with scholars based in Netherlands, United States and United Kingdom. D. J. J. Halley's 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 and has published in prestigious journals such as Biochemical and Biophysical Research Communications, Annals of the New York Academy of Sciences and The American Journal of Human Genetics.

In The Last Decade

D. J. J. Halley

38 papers receiving 1.2k citations

Peers

D. J. J. Halley

GENET

PHYSI

PRM

Armand Bottani Switzerland

Jean‐Pierre Fryns Belgium

Kwame Anyane‐Yeboa United States

R. J. M. Gardner New Zealand

Bertrand Isidor France

A.M.W. van den Ouweland Netherlands

Mitsuo Masuno Japan

David Geneviève France

Phillip J. Dexheimer United States

Armand Bottani Switzerland

D. J. J. Halley

1.3k ×2.4

GENET

1.2k ×2.3

176 ×0.7

PHYSI

76 ×0.4

88 ×0.5

PRM

Citations per year, relative to D. J. J. Halley D. J. J. Halley (= 1×) peers Armand Bottani

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

Verhoef, Senno, Tadeusz Mazurczak, Sergiusz Jóźwiak, et al.. (1999). High Rate of Mosaicism in Tuberous Sclerosis Complex. The American Journal of Human Genetics. 64(6). 1632–1637. 121 indexed citations

Verhoef, Senno, W.L. Akkersdijk, N. M. A. Bax, et al.. (1999). Malignant pancreatic tumour within the spectrum of tuberous sclerosis complex in childhood. European Journal of Pediatrics. 158(4). 284–287. 82 indexed citations

Dohle, Gert R., Shelley E. Overbeek, A.M.W. van den Ouweland, et al.. (1999). The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic data. Human Reproduction. 14(2). 371–374. 39 indexed citations

Vries, Bert Ba de, D. J. J. Halley, Ben A. Oostra, & Martinus F. Niermeijer. (1998). The fragile X syndrome.. Journal of Medical Genetics. 35(7). 579–589. 190 indexed citations

Cnossen, Marjon H., Martijn H. Breuning, Christi J. van Asperen, et al.. (1997). Deletions spanning the neurofibromatosis type 1 gene: Implications for genotype-phenotype correlations in neurofibromatosis type 1?. Human Mutation. 9(5). 458–464. 92 indexed citations

Hornigold, Nick, Marjon van Slegtenhorst, Joseph Nahmias, et al.. (1997). A 1.7-Megabase Sequence-Ready Cosmid Contig Covering the TSC1 Candidate Region in 9q34. Genomics. 41(3). 385–389. 14 indexed citations

Kwiatkowska, J., Elizabeth P. Henske, J. L. Haines, et al.. (1997). Cloning and evaluation of RALGDS as a candidate for the tuberous sclerosis gene TSC1. Annals of Human Genetics. 61(4). 299–305. 6 indexed citations

Beuten, Joke, Raoul C. M. Hennekam, Bernadette Van Roy, et al.. (1996). Angelman syndrome in an inbred family. Human Genetics. 97(3). 294–298. 3 indexed citations

Milewski, Michał, Jerzy Bal, Wout H. Deelen, et al.. (1996). Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndrome.. Acta Biochimica Polonica. 43(2). 383–388. 1 indexed citations

10.

Duits, Annelien, Rob Willemsen, J. O. Van Hemel, et al.. (1996). Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family.. Journal of Medical Genetics. 33(12). 1007–1010. 62 indexed citations

11.

Swaay, Eveline Wesby–van, Frans J. Los, J. O. Van Hemel, et al.. (1995). DNA diagnosis of Prader-Willi and Angelman syndromes with the probe PW71 (D15S63). Human Genetics. 95(5). 562–567. 12 indexed citations

12.

Vries, Bert Ba de, J. P. Fryns, Merlin G. Butler, et al.. (1993). Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.. Journal of Medical Genetics. 30(9). 761–766. 73 indexed citations

13.

Lindhout, Dick, et al.. (1992). In search for genes predisposing to epilepsy: Motives and methods. Acta Neurologica Scandinavica. 86(S140). 51–58. 1 indexed citations

14.

Oostra, B. A., J.F. de Rijk-van Andel, H. J. Eussen, et al.. (1991). DNA analysis in patients with lissencephaly type I and other cortical dysplasias. American Journal of Medical Genetics. 40(3). 383–386. 5 indexed citations

15.

Andel, J.F. de Rijk-van, Coriene E. Catsman‐Berrevoets, D. J. J. Halley, et al.. (1991). Isolated lissencephaly sequence associated with a microdeletion at chromosome 17p13. Human Genetics. 87(4). 509–510. 5 indexed citations

16.

Povey, Sue, Mari‐Wyn Burley, M. Smith, et al.. (1991). An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two‐Point Methods^a. Annals of the New York Academy of Sciences. 615(1). 298–305. 16 indexed citations

17.

Povey, Sue, L. A. Sandkuyl, Dick Lindhout, et al.. (1991). A Comparative Study on Genetic Heterogeneity in Tuberous Sclerosis: Evidence for One Gene on 9q34 and a Second Gene on 11q22–23^a. Annals of the New York Academy of Sciences. 615(1). 306–315. 22 indexed citations

18.

Oostra, B. A., Coen A. M. van Bennekom, Egbert Bakker, et al.. (1990). New polymorphic DNA marker close to the fragile site FRAXA. Genomics. 6(1). 129–132. 49 indexed citations

19.

Halley, D. J. J., Henk J. Veeze, L. A. Sandkuyl, et al.. (1990). The mutation ΔF508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosis. Human Genetics. 85(4). 407–408. 8 indexed citations

20.

Morreau, J., M. Sinaasappel, Ben A. Oostra, & D. J. J. Halley. (1988). Cystic fibrosis: screening for a DNA deletion by field inversion gel electrophoresis. Human Genetics. 79(1). 64–67. 3 indexed citations

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