Dicky Halley

10.5k citations

128 papers · 5.0k · h-index 36

Impact in

Physiology top 0.5%
- Tuberous Sclerosis Complex Research
- Lysosomal Storage Disorders Research
- Histiocytic Disorders and Treatments
Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities

Papers in

Physiology 46
- Tuberous Sclerosis Complex Research 30
- Lysosomal Storage Disorders Research 15
- Histiocytic Disorders and Treatments 11
Genetics 39
- Genomic variations and chromosomal abnormalities 17
- Genetics and Neurodevelopmental Disorders 16

Co-authors: Mark Nellist (28 shared papers)Ans van den Ouweland (17 shared papers)Ans M.W. van den Ouweland (17 shared papers)Miriam Goedbloed (10 shared papers)Martinus F. Niermeijer (13 shared papers)Bernard A. Zonnenberg (5 shared papers)Henk J. Veeze (8 shared papers)Senno Verhoef (7 shared papers)
Journals: European Journal of Human Genetics (12 papers)Human Mutation (10 papers)Prenatal Diagnosis (9 papers)Human Genetics (8 papers)Journal of Medical Genetics (4 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Dicky Halley

124 papers receiving 4.9k citations

Peers

Countries citing papers authored by Dicky Halley

Since Specialization

Citations

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

Fields of papers citing papers by Dicky Halley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Dicky Halley, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Dicky Halley Line = papers co-authored together Dicky Halley links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 128 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype – phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex European Journal of Human Genetics ·Őzgür Sancak, Mark Nellist, Miriam Goedbloed, Peter Elfferich, (unknown), Anneke Maat‐Kievit, Bernard A. Zonnenberg, Senno Verhoef, Dicky Halley, Ans van den Ouweland	2005	351
2	The tuberous sclerosis-1 (TSC1) gene product hamartin suppresses cell growth and augments the expression of the TSC2 product tuberin by inhibiting its ubiquitination Oncogene ·Giovanna Benvenuto, Shaowei Li, Samantha J Brown, Richard Braverman, William C. Vass, Jeremy P. Cheadle, Dicky Halley, Julian R. Sampson, Ralf Wienecke, Jeffrey E. DeClue	2000	204
3	Mental status of females with an FMR1 gene full mutation. PubMed ·Bert Ba de Vries, A. M. Wiegers, Apt Smits, Serieta Mohkamsing, H.J. Duivenvoorden, J. P. Fryns, Lmg Curfs, Dicky Halley, B. A. Oostra, Ans MW van den Ouweland, Martinus F. Niermeijer	1996	165
4	Screening and Diagnosis for the Fragile X Syndrome among the Mentally Retarded: An Epidemiological and Psychological Survey The American Journal of Human Genetics ·Bert de Vries, Ans M.W. van den Ouweland, Serieta Mohkamsing, Hugo J. Duivenvoorden, Esther Mol, Kirsten Gelsema, Monique van Rijn, Dicky Halley, Lodewijk A. Sandkuijl, Ben A. Oostra, Aad Tibben, Martinus F. Niermeijer	1997	159
5	Cognitive impairment in tuberous sclerosis complex is a multifactorial condition Neurology ·Floor E. Jansen, Koen L. Vincken, Ale Algra, Petronella Anbeek, Olga Braams, Mark Nellist, Bernard A. Zonnenberg, (unknown), Ans van den Ouweland, Dicky Halley, Alexander C. van Huffelen, Onno van Nieuwenhuizen	2007	158
6	Characterization of the Cytosolic Tuberin-Hamartin Complex Journal of Biological Chemistry ·Mark Nellist, Marjon A. van Slegtenhorst, Miriam Goedbloed, Ans M.W. van den Ouweland, Dicky Halley, Peter van der Sluijs	1999	149
7	Mucopolysaccharidosis type IIIA: Clinical spectrum and genotype‐phenotype correlations Annals of Neurology ·M. J. Valstar, Sanne Neijs, Hennie T. Brüggenwirth, Renske Olmer, George J. G. Ruijter, Ron A. Wevers, Otto P. van Diggelen, Ben J. H. M. Poorthuis, Dicky Halley, Frits A. Wijburg	2010	146
8	Common C-to-T Substitution at Position −480 of the Hepatic Lipase Promoter Associated With a Lowered Lipase Activity in Coronary Artery Disease Patients Arteriosclerosis Thrombosis and Vascular Biology ·Hans Jansen, Adrie J.M. Verhoeven, Lilian Weeks, John J.P. Kastelein, Dicky Halley, Ans van den Ouweland, J. Wouter Jukema, (unknown), J.C. Birkenhäger	1997	143
9	17β-Hydroxysteroid Dehydrogenase-3 Deficiency: Diagnosis, Phenotypic Variability, Population Genetics, and Worldwide Distribution of Ancient and de Novo Mutations1 The Journal of Clinical Endocrinology & Metabolism ·Annemie L. M. Boehmer, Albert O. Brinkmann, Lodewijk A. Sandkuijl, Dicky Halley, Martinus F. Niermeijer, Stefan Andersson, Frank H. de Jong, Hülya Kayserili, Monique A. de Vroede, Barto J. Otten, Catrienus W. Rouwé, Berenice B. Mendonça, Cidade Rodrigues, Hans H. Bode, Petra E. de Ruiter, Henriëtte A. Delemarre‐van de Waal, Stenvert L. S. Drop	1999	141
10	Broad spectrum of Pompe disease in patients with the same c.-32-13T→G haplotype Neurology ·Marian A. Kroos, Robert J. Pomponio, M.L.C. Hagemans, J. L. M. Keulemans, Michael Phipps, Matthew DeRiso, Rachel Palmer, M.G.E.M. Ausems, Nadine A. M. E. van der Beek, O. P. van Diggelen, Dicky Halley, Ans T. van der Ploeg, A. J. J. Reuser	2007	136
11	Survival in Hereditary Breast Cancer Associated With Germline Mutations of BRCA2 Journal of Clinical Oncology ·L.C. Verhoog, Cecile T.M. Brekelmans, Caroline Seynaeve, G Dahmen, A.N. van Geel, C.C.M. Bartels, Madeleine M.A. Tilanus‐Linthorst, Anja Wagner, Peter Devilee, Dicky Halley, A.M.W. van den Ouweland, E.J. Meijers-Heijboer, J.G.M. Klijn	1999	134
12	A Cystic Fibrosis Mutation Associated with Mild Lung Disease New England Journal of Medicine ·K. H. Gan, Henk J. Veeze, Ans van den Ouweland, Dicky Halley, Hans Scheffer, Annemieke van der Hout, Shelley E. Overbeek, Johan C. de Jongste, Willem H. Bakker, Harry Heijerman	1995	122
13	Chloride conductance and genetic background modulate the cystic fibrosis phenotype of ΔF508 homozygous twins and siblings Journal of Clinical Investigation ·Inez Bronsveld, Frauke Mekus, Jan Bijman, Manfred Ballmann, Hugo R. de Jonge, Ulrike Laabs, Dicky Halley, Helmut Ellemunter, G. Mastella, Stephen H. Thomas, Henk J. Veeze, Burkhard Tümmler	2001	111
14	Update of the Pompe disease mutation database with 107 sequence variants and a format for severity rating Human Mutation ·Marian A. Kroos, Robert J. Pomponio, Laura Van de Vliet, Rachel Palmer, Michael Phipps, Robert van der Helm, Dicky Halley, Arnold Reuser	2008	106
15	Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation Journal of Medical Genetics ·Marjon van Slegtenhorst, Senno Verhoef, A.M.P. Tempelaars, Lida Bakker, Qi Wang, Marja W. Wessels, Remco Bakker, Mark Nellist, Dick Lindhout, Dicky Halley, Ans van den Ouweland	1999	105
16	Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotype. Journal of Clinical Investigation ·Henk J. Veeze, Dicky Halley, Jan Bijman, J.C. de Jongste, Hugo R. de Jonge, M. Sinaasappel	1994	105
17	Mucopolysaccharidosis type IIIB may predominantly present with an attenuated clinical phenotype Journal of Inherited Metabolic Disease ·M. J. Valstar, Hennie T. Brüggenwirth, Renske Olmer, Ron A. Wevers, Frans W. Verheijen, Ben J. H. M. Poorthuis, Dicky Halley, Frits A. Wijburg	2010	93
18	A prospective 10 year follow up study of patients with neurofibromatosis type 1 Archives of Disease in Childhood ·Marjon H. Cnossen, Arja de Goede-Bolder, K M van den Broek, C M E Waasdorp, A. P. Oranje, Hans Stroink, Huibert J. Simonsz, A.M.W. van den Ouweland, Dicky Halley, Martinus F. Niermeijer	1998	85
19	Overlapping neurologic and cognitive phenotypes in patients with TSC1 or TSC2 mutations Neurology ·Floor E. Jansen, Olga Braams, Koen L. Vincken, Ale Algra, Petronella Anbeek, (unknown), Dicky Halley, Bernard A. Zonnenberg, Ans van den Ouweland, Alexander C. van Huffelen, Onno van Nieuwenhuizen, Mark Nellist	2007	76
20	COL4A2 mutation associated with familial porencephaly and small-vessel disease European Journal of Human Genetics ·Elly Verbeek, Marije Meuwissen, Frans W. Verheijen, Paul Govaert, Daniel J. Licht, Debbie S. Kuo, Cathryn Poulton, Rachel Schot, Maarten H. Lequin, Jeroen Dudink, Dicky Halley, I.F.M. de Coo, Jan C. den Hollander, Renske Oegema, Douglas B. Gould, Grazia M.S. Mancini	2012	75

About Dicky Halley

Dicky Halley is a scholar working on Physiology, Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine, having authored 128 papers that have together received 5.0k indexed citations. Recurring topics across this work include Tuberous Sclerosis Complex Research (30 papers), Genomic variations and chromosomal abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (16 papers), Lysosomal Storage Disorders Research (15 papers), Prenatal Screening and Diagnostics (12 papers), Cystic Fibrosis Research Advances (12 papers), Histiocytic Disorders and Treatments (11 papers) and Autism Spectrum Disorder Research (9 papers). The work is most often cited by research in Physiology (2.0k citations), Genetics (1.4k citations), Rheumatology (344 citations), Molecular Biology (1.5k citations) and Neurology (300 citations). Dicky Halley has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Mark Nellist, Ans van den Ouweland, Ans M.W. van den Ouweland, Miriam Goedbloed, Martinus F. Niermeijer, Bernard A. Zonnenberg, Henk J. Veeze, Senno Verhoef, Anneke Maat‐Kievit and Őzgür Sancak. Their work appears in journals such as European Journal of Human Genetics, Human Mutation, Prenatal Diagnosis, Human Genetics and Journal of Medical 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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Dicky Halley

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