Duncan P. McHale

2.9k citations

11 papers · 1.8k indexed · 1 hit paper · h-index 9

Molecular Biology top 10%
Physiology top 5%
Cellular and Molecular Neuroscience top 5%
Neurology top 2%
Genetics top 10%

Co-authors: C. Geoffrey Woods Hussain Jafri Gulshan Karbani Emma Roberts Kelly Springell John N. Wood Enza Maria Valente Richard Williams
Topics: RNA regulation and disease (2 papers)Chromosomal and Genetic Variations (2 papers)Microtubule and mitosis dynamics (2 papers)
Cited by: Neurology Sensory Systems Cellular and Molecular Neuroscience
Journals: Nature Nature Genetics The American Journal of Human Genetics
Partner nations: United Kingdom Pakistan United States

In The Last Decade

Duncan P. McHale

11 papers receiving 1.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

An SCN9A channelopathy causes congenital inability to experience pain

2006 1.1k citations James J. Cox, Frank Reimann et al. Nature profile →

Peers

Countries citing papers authored by Duncan P. McHale

Since Specialization

Citations

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

Fields of papers citing papers by Duncan P. McHale

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Duncan P. McHale. 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 Duncan P. McHale. The network helps show where Duncan P. McHale may publish in the future.

Co-authorship network of co-authors of Duncan P. McHale

This figure shows the co-authorship network connecting the top 25 collaborators of Duncan P. McHale. A scholar is included among the top collaborators of Duncan P. McHale 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 Duncan P. McHale. Duncan P. McHale is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

#	Work	Indexed citations
1	Association between neprilysin polymorphisms and sporadic Alzheimer's disease 2007 ·Neuroscience Letters ·Linda S. Wood,Eve H. Pickering,Duncan P. McHale,Bryan Dechairo	21
2	An SCN9A channelopathy causes congenital inability to experience painbreakdown → 2006 ·Nature ·James J. Cox,Frank Reimann,Adeline K. Nicholas,(unknown),Emma Roberts,Kelly Springell,Gulshan Karbani,Hussain Jafri,(unknown),Yasmin Raashid,Lihadh Al‐Gazali,(unknown),Enza Maria Valente,Shaun Gorman,Richard Williams,Duncan P. McHale,John N. Wood,Fiona M. Gribble,C. Geoffrey Woods	1094
3	Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease 2001 ·Nature Genetics ·Andrew R.J. Curtis,(unknown),Christopher M. Morris,Laurence A. Bindoff,Paul G. Ince,Patrick F. Chinnery,Alan Coulthard,Margaret Jackson,Andrew P. Jackson,Duncan P. McHale,(unknown),William Barker,Alex Markham,David Bates,Ann Curtis,John Burn	386
4	A Gene for Autosomal Recessive Symmetrical Spastic Cerebral Palsy Maps to Chromosome 2q24-25 1999 ·The American Journal of Human Genetics ·Duncan P. McHale,Simon J Mitchell,Sarah Bundey,Leanne Moynihan,David A. Campbell,C. Geoffrey Woods,Nicholas Lench,R F Mueller,A.F. Markham	37
5	The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1–13.2 1999 ·European Journal of Human Genetics ·Emma Roberts,Andrew P. Jackson,(unknown),(unknown),(unknown),Yasmin Abdul Rashid,Hussain Jafri,Duncan P. McHale,Alex Markham,Nicholas Lench,C. Geoffrey Woods	79
6	Primary Autosomal Recessive Microcephaly (MCPH1) Maps to Chromosome 8p22-pter 1998 ·The American Journal of Human Genetics ·Andrew P. Jackson,Duncan P. McHale,David A. Campbell,Hussain Jafri,Yasmin Abdul Rashid,(unknown),Gulshan Karbani,Peter Corry,Malcolm I. Levene,Robert F. Mueller,(unknown),Nicholas Lench,C. Geoffrey Woods	117
7	A Syndrome of Severe Mental Retardation, Spasticity, and Tapetoretinal Degeneration Linked to Chromosome 15q24 1998 ·The American Journal of Human Genetics ·Simon J. Mitchell,Duncan P. McHale,David A. Campbell,Nicholas Lench,R F Mueller,Sarah Bundey,Alex Markham	14
8	Autozygosity Mapping, to Chromosome 11q25, of a Rare Autosomal Recessive Syndrome Causing Histiocytosis, Joint Contractures, and Sensorineural Deafness 1998 ·The American Journal of Human Genetics ·Leanne Moynihan,Sarah Bundey,(unknown),(unknown),Duncan P. McHale,Robert F. Mueller,Alexander F. Markham,Nicholas Lench	27
9	A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22. 1997 ·Journal of Medical Genetics ·David A. Campbell,Duncan P. McHale,Kathryn Brown,Leanne Moynihan,Mark Houseman,Gulshan Karbani,G. Parry,(unknown),Valerie Newton,(unknown),Alex Markham,Nicholas Lench,R F Mueller	31
10	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
11	Further evidence of genetic heterogeneity in hereditary hydronephrosis 1996 ·Clinical Genetics ·Duncan P. McHale,Mary Porteous,(unknown),(unknown)	4

About Duncan P. McHale

Duncan P. McHale is a scholar working on Sensory Systems, Immunology and Allergy and Urology, having authored 11 papers that have together received 1.8k indexed citations. Recurring topics across this work include RNA regulation and disease (2 papers), Chromosomal and Genetic Variations (2 papers) and Microtubule and mitosis dynamics (2 papers). The work is most often cited by research in Neurology (305 citations), Sensory Systems (143 citations) and Cellular and Molecular Neuroscience (526 citations). Duncan P. McHale has collaborated with scholars based in United Kingdom, Pakistan and United States. Frequent co-authors include C. Geoffrey Woods, Hussain Jafri, Gulshan Karbani, Emma Roberts, Kelly Springell, John N. Wood, Enza Maria Valente, Richard Williams, Lihadh Al‐Gazali and Yasmin Raashid. Their work appears in journals such as Nature, Nature Genetics 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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