Kit Doudney

1.2k citations

25 papers · 762 indexed · h-index 13

Impact in

Genetics top 10%
- Cleft Lip and Palate Research
- Craniofacial Disorders and Treatments
Molecular Biology
- Congenital heart defects research
- Developmental Biology and Gene Regulation
- Wnt/β-catenin signaling in development and cancer
- Mitochondrial Function and Pathology
- dental development and anomalies

Papers in ⓘ

Cellular and Molecular Neuroscience 6
- Genetic Neurodegenerative Diseases 6
Genetics 9
- Genetics and Neurodevelopmental Disorders 3
- Genomic variations and chromosomal abnormalities 3

Co-authors: Philip Stanier (10 shared papers)Gudrun E. Moore (4 shared papers)Andrew J. Copp (6 shared papers)Claire Braybrook (2 shared papers)Michael A. Patton (1 shared paper)Ana Carolina B. Marçano (1 shared paper)Alfreð Árnason (1 shared paper)Paul J. Goodfellow (1 shared paper)
Journals: Nature Genetics (3 papers)Genomics (3 papers)BMJ Open (1 paper)Scientific Reports (1 paper)Human Molecular Genetics (1 paper)
Partner nations: United Kingdom New Zealand United States

In The Last Decade

Kit Doudney

25 papers receiving 742 citations

Peers

Countries citing papers authored by Kit Doudney

Since Specialization

Citations

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

Fields of papers citing papers by Kit Doudney

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Kit Doudney, 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 Kit Doudney Line = papers co-authored together Kit Doudney 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 25 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia Nature Genetics ·Claire Braybrook, Kit Doudney, Ana Carolina B. Marçano, Alfreð Árnason, Árni Björnsson, Michael A. Patton, Paul J. Goodfellow, Gudrun E. Moore, Philip Stanier	2001	206
2	Mutations in the planar cell polarity genesCELSR1andSCRIBare associated with the severe neural tube defect craniorachischisis Human Mutation ·Alexis Robinson, Sarah Escuin, Kit Doudney, Michel Vekemans, Roger E. Stevenson, Nicholas D. E. Greene, Andrew J. Copp, Philip Stanier	2011	146
3	TBX22 Missense Mutations Found in Patients with X-Linked Cleft Palate Affect DNA Binding, Sumoylation, and Transcriptional Repression The American Journal of Human Genetics ·Artemisia M. Andreou, Erwin Pauws, Marius C. Jones, Manvendra K. Singh, Markus Bussen, Kit Doudney, Gudrun E. Moore, Andreas Kispert, Jan J. Brosens, Philip Stanier	2007	69
4	The Friedreich's ataxia gene encodes a novel phosphatidylinositol–4–phosphate 5–kinase Nature Genetics ·Jaime J. Carvajal, Mark A. Pook, Maria dos Remédios Magalhães Santos, Kit Doudney, Renate Hillermann, Shane Minogue, Robert Williamson, J. Justin Hsuan, Susan Chamberlain	1996	61
5	Abnormal folate metabolism in foetuses affected by neural tube defects Brain ·Louisa P.E. Dunlevy, Lyn S. Chitty, Katie A. Burren, Kit Doudney, T. Stojilkovic‐Mikic, Philip Stanier, Richard H. Scott, Andrew J. Copp, Nicholas D. E. Greene	2006	43
6	Epithelial cell polarity genes are required for neural tube closure American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Kit Doudney, Philip Stanier	2005	36
7	G-Quadruplex Structures and CpG Methylation Cause Drop-Out of the Maternal Allele in Polymerase Chain Reaction Amplification of the Imprinted MEST Gene Promoter PLoS ONE ·Aaron J. Stevens, Selma Stuffrein-Roberts, Simone L. Cree, Andrew Gibb, Allison L. Miller, Kit Doudney, Alan Aitchison, Michael R. Eccles, Peter R. Joyce, Vyacheslav V. Filichev, Martin A. Kennedy	2014	32
8	Cloning and Characterization of Igsf9 in Mouse and Human: A New Member of the Immunoglobulin Superfamily Expressed in the Developing Nervous System Genomics ·Kit Doudney, J. Murdoch, Claire Braybrook, Caroline Paternotte, Louise Bentley, Andrew J. Copp, Philip Stanier	2002	26
9	Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9q. PubMed ·Susan Chamberlain, Martin Farrall, Jacqui Shaw, David Wilkes, Jaime J. Carvajal, Renate Hillerman, Kit Doudney, A E Harding, Robert Williamson, Giorgio Sirugo	1993	25
10	Friedreich's ataxia: a defect in signal transduction? Human Molecular Genetics ·Jaime J. Carvajal, Mark A. Pook, Kit Doudney, Renate Hillermann, David Wilkes, Sahar Al‐Mahdawi, Robert Williamson, Susan Chamberlain	1995	22
11	Valproic acid exposure leads to upregulation and increased promoter histone acetylation of sepiapterin reductase in a serotonergic cell line Neuropharmacology ·Diana Balasubramanian, Alicia X. Deng, Kit Doudney, Mark B. Hampton, Martin A. Kennedy	2015	20
12	Autosomal-dominant Ankyloglossia and Tooth Number Anomalies Journal of Dental Research ·Ana Carolina Acevedo, Janaína Aparecida Calaça da Fonseca, J. Grinham, Kit Doudney, Raquel Ribeiro Gomes, L.M. Paula, Philip Stanier	2009	14
13	Comparative Physical and Transcript Maps of ∼1 Mb around loop-tail, a Gene for Severe Neural Tube Defects on Distal Mouse Chromosome 1 and Human Chromosome 1q22–q23 Genomics ·Kit Doudney, J. Murdoch, Caroline Paternotte, Louise Bentley, Simon G. Gregory, Andrew J. Copp, Philip Stanier	2001	13
14	Comparing the variants of takotsubo syndrome: an observational study of the ECG and structural changes from a New Zealand tertiary hospital BMJ Open ·George M. Watson, Christina Chan, Laura M. Belluscio, Kit Doudney, Cameron Lacey, Martin A. Kennedy, Paul Bridgman	2019	10
15	Genomic organization and embryonic expression of igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia Molecular and Cellular Neuroscience ·J. Murdoch, Kit Doudney, Dianne Gerrelli, Noel C. Wortham, Caroline Paternotte, Philip Stanier, Andrew J. Copp	2003	9
16	A family with pseudodominant Friedreich's ataxia showing marked variation of phenotype between affected siblings Journal of Neurology Neurosurgery & Psychiatry ·Simon P. Webb, Kit Doudney, Mark A. Pook, S. Chamberlain, Michael Hutchinson	1999	9
17	Copy number variants implicate cardiac function and development pathways in earthquake-induced stress cardiomyopathy Scientific Reports ·Cameron Lacey, Kit Doudney, Paul Bridgman, Peter M. George, Roger Mulder, Julie J. Zarifeh, Bridget Kimber, Murray Cadzow, Michael A. Black, Tony R. Merriman, Klaus Lehnert, Vivienne M. Bickley, John F. Pearson, Vicky A. Cameron, Martin A. Kennedy	2018	7
18	Analysis of the planar cell polarity gene Vangl2 and its co‐expressed paralog Vangl1 in neural tube defect patients (Am J Med Genet 136A: 90–92, 2005) American Journal of Medical Genetics Part A ·Kit Doudney, Gudrun E. Moore, Philip Stanier, Patricia Ybot‐González, Caroline Paternotte, Nicholas D. E. Greene, Andrew J. Copp, Roger E. Stevenson	2005	3
19	Exome sequencing and array-based comparative genomic hybridisation analysis of preferential 6-methylmercaptopurine producers The Pharmacogenomics Journal ·Eng Wee Chua, Simone L. Cree, Murray L. Barclay, Kit Doudney, Klaus Lehnert, Alan Aitchison, Martin A. Kennedy	2015	2
20	Exon–Intron Structure of a 2.7-kb Transcript of the STM7 Gene with Phosphatidylinositol-4-phosphate 5-Kinase Activity Genomics ·Mark A. Pook, Jaime J. Carvajal, Kit Doudney, Renate Hillermann, Susan Chamberlain	1997	2

About Kit Doudney

Kit Doudney is a scholar working on Cellular and Molecular Neuroscience, Genetics, Cell Biology, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 25 papers that have together received 762 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (6 papers), Congenital heart defects research (4 papers), Wnt/β-catenin signaling in development and cancer (3 papers), Prenatal Screening and Diagnostics (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Pharmacological Effects and Toxicity Studies (2 papers). The work is most often cited by research in Genetics (298 citations), Molecular Biology (500 citations), Cell Biology (117 citations), Aging (12 citations) and Cellular and Molecular Neuroscience (123 citations). Kit Doudney has collaborated with scholars based in United Kingdom, New Zealand and United States. Frequent co-authors include Philip Stanier, Gudrun E. Moore, Andrew J. Copp, Claire Braybrook, Michael A. Patton, Ana Carolina B. Marçano, Alfreð Árnason, Paul J. Goodfellow, Árni Björnsson and Nicholas D. E. Greene. Their work appears in journals such as Nature Genetics, Genomics, BMJ Open, Scientific Reports and Human Molecular 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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