Neil V. Whittock

1.9k citations

34 papers · 1.4k indexed · h-index 19

Co-authors: John A. McGrath Robin A.J. Eady Peter D. Turnpenny Sian Ellard Sally L. Dunwoodie Kenro Kusumi Duncan B. Sparrow Merridee A. Wouters
Topics: Skin and Cellular Biology Research (16 papers)Wnt/β-catenin signaling in development and cancer (11 papers)Autoimmune Bullous Skin Diseases (5 papers)
Cited by: Cell Biology Physiology Urology
Journals: Journal of Biological Chemistry Journal of Clinical Investigation Biochemical and Biophysical Research Communications
Partner nations: United Kingdom United States Australia

In The Last Decade

Neil V. Whittock

34 papers receiving 1.3k citations

Peers

Countries citing papers authored by Neil V. Whittock

Since Specialization

Citations

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

Fields of papers citing papers by Neil V. Whittock

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Neil V. Whittock. 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 Neil V. Whittock. The network helps show where Neil V. Whittock may publish in the future.

Co-authorship network of co-authors of Neil V. Whittock

This figure shows the co-authorship network connecting the top 25 collaborators of Neil V. Whittock. A scholar is included among the top collaborators of Neil V. Whittock 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 Neil V. Whittock. Neil V. Whittock 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	Mutation of the LUNATIC FRINGE Gene in Humans Causes Spondylocostal Dysostosis with a Severe Vertebral Phenotype 2005 ·The American Journal of Human Genetics ·Duncan B. Sparrow,Gavin Chapman,Merridee A. Wouters,Neil V. Whittock,Sian Ellard,Diane Fatkin,Peter D. Turnpenny,Kenro Kusumi,Daniel J. Sillence,Sally L. Dunwoodie	182
2	Defining the pathogenic involvement of desmoglein 4 in pemphigus and staphylococcal scalded skin syndrome 2004 ·Journal of Clinical Investigation ·Takeshi Nagasaka,Koji Nishifuji,Takayuki Ota,Neil V. Whittock,Masayuki Amagai	43
3	Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis 2003 ·Journal of Medical Genetics ·Peter D. Turnpenny,Neil V. Whittock,(unknown),Sally L. Dunwoodie,Kenro Kusumi,Sian Ellard	100
4	Targetting of desmoglein 1 in inherited and acquired skin diseases 2003 ·Clinical and Experimental Dermatology ·Neil V. Whittock,Chris Bower	26
5	Molecular genetic prenatal diagnosis for a case of autosomal recessive spondylocostal dysostosis 2003 ·Prenatal Diagnosis ·Neil V. Whittock,Peter D. Turnpenny,J.H.A.M. Tuerlings,Sian Ellard	8
6	Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles 2002 ·Journal of Investigative Dermatology ·Rebecca M. Porter,Declan P. Lunny,(unknown),(unknown),Neil Wilson,E. Birgitte Lane,Colin A.B. Jahoda,W.H. Irwin McLean,Neil V. Whittock,Julia Reichelt,Thomas M. Magin	45
7	Refined Mapping of Naegeli–Franceschetti– Jadassohn Syndrome to a 6 cM Interval on Chromosome 17q11.2-q21 and Investigation of Candidate Genes 2002 ·Journal of Investigative Dermatology ·Eli Sprecher,Jouni Uitto,Gabriele Richard,Peter Itin,Neil V. Whittock,John A. McGrath,(unknown),John J. DiGiovanna,Sherri J. Bale	27
8	Frameshift Mutation in the V2 Domain of Human Keratin 1 Results in Striate Palmoplantar Keratoderma 2002 ·Journal of Investigative Dermatology ·Neil V. Whittock,Frances J.D. Smith,W.H. Irwin McLean,Hong Wan,(unknown),W.A.D. Griffiths,Patricia J.C. Dopping-Hepenstal,G H S Ashton,Robin A.J. Eady,John A. McGrath	70
9	Frameshift mutation in the V2 domain of keratin I causes the striate form of palmoplantar keratoderma 2001 ·Journal of Investigative Dermatology ·Neil V. Whittock,Huiying Wan,Frances J.D. Smith,Fergus Keane,(unknown),(unknown),P. J. Dopping-Hepenstal,G H S Ashton,Robin A.J. Eady,W.H. Irwin McLean,John A. McGrath	2
10	Genomic localization, organization and amplification of the human zinc transporter protein gene, ZNT4 , and exclusion as a candidate gene in different clinical variants of acrodermatitis enteropathica 2001 ·Archives of Dermatological Research ·O. Bleck,G H S Ashton,(unknown),Andrew P. South,Neil V. Whittock,W.H. Irwin McLean,David J. Atherton,John A. McGrath	10
11	New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens. 2001 ·British Journal of Dermatology ·Neil V. Whittock,G H S Ashton,W.A.D. Griffiths,Robin A.J. Eady,John A. McGrath	18
12	Genomic Amplification of the Human Plakophilin 1 Gene and Detection of a New Mutation in Ectodermal Dysplasia/Skin Fragility Syndrome 2000 ·Journal of Investigative Dermatology ·Neil V. Whittock,Robin A.J. Eady,John A. McGrath,Marek Haftek,(unknown),(unknown),H Perrot	59
13	Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes 2000 ·Biochemical and Biophysical Research Communications ·Neil V. Whittock,Robin A.J. Eady,John A. McGrath	12
14	Genomic Organization and Amplification of the Human Epidermal Type II Keratin Genes K1 and K5 2000 ·Biochemical and Biophysical Research Communications ·Neil V. Whittock,Robin A.J. Eady,John A. McGrath	16
15	The Gene for Naegeli–Franceschetti–Jadassohn Syndrome Maps to 17q21 2000 ·Journal of Investigative Dermatology ·Neil V. Whittock,G H S Ashton,Robin A.J. Eady,John A. McGrath,Carrie M. Coleman,W.H. Irwin McLean,K. Acland	12
16	Genomic organization and amplification of the human plakoglobin gene (JUP) 2000 ·Experimental Dermatology ·Neil V. Whittock,Robin A.J. Eady,John A. McGrath	12
17	Striate Palmoplantar Keratoderma Resulting from Desmoplakin Haploinsufficiency 1999 ·Journal of Investigative Dermatology ·Neil V. Whittock,G H S Ashton,Patricia J.C. Dopping-Hepenstal,Matthew J. Gratian,Fiona M. Keane,Robin A.J. Eady,John A. McGrath	111
18	Comparative Mutation Detection Screening of the Type VII Collagen Gene (COL7A1) Using the Protein Truncation Test, Fluorescent Chemical Cleavage of Mismatch, and Conformation Sensitive Gel Electrophoresis 1999 ·Journal of Investigative Dermatology ·Neil V. Whittock,(unknown),(unknown),Jemima E. Mellerio,Christopher G. Mathew,Stephen Abbs,Robin A.J. Eady,John A. McGrath	66
19	Dystrophin Point Mutation Screening Using a Multiplexed Protein Truncation Test 1997 ·Genetic Testing ·Neil V. Whittock,Roland G. Roberts,Christopher G. Mathew,Stephen Abbs	23
20	Mutation analysis 1996 ·Journal of Medical Genetics ·Neil V. Whittock,Roland G. Roberts,(unknown),Duncan P. McHale,(unknown),Müeller,(unknown),(unknown),(unknown),Muñóz,(unknown),(unknown),(unknown),(unknown),(unknown)	1

About Neil V. Whittock

Neil V. Whittock is a scholar working on Cell Biology, Urology and Genetics, having authored 34 papers that have together received 1.4k indexed citations. Recurring topics across this work include Skin and Cellular Biology Research (16 papers), Wnt/β-catenin signaling in development and cancer (11 papers) and Autoimmune Bullous Skin Diseases (5 papers). The work is most often cited by research in Cell Biology (494 citations), Physiology (97 citations) and Urology (105 citations). Neil V. Whittock has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include John A. McGrath, Robin A.J. Eady, Peter D. Turnpenny, Sian Ellard, Sally L. Dunwoodie, Kenro Kusumi, Duncan B. Sparrow, Merridee A. Wouters, G H S Ashton and W.H. Irwin McLean. Their work appears in journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Biochemical and Biophysical Research Communications.

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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