Duncan P. McHale

2.9k total citations · 1 hit paper
11 papers, 1.8k citations indexed

About

Duncan P. McHale is a scholar working on Molecular Biology, Physiology and Sensory Systems. According to data from OpenAlex, Duncan P. McHale has authored 11 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 3 papers in Physiology and 2 papers in Sensory Systems. Recurrent topics in Duncan P. McHale's work include RNA regulation and disease (2 papers), Chromosomal and Genetic Variations (2 papers) and Microtubule and mitosis dynamics (2 papers). Duncan P. McHale is often cited by papers focused on RNA regulation and disease (2 papers), Chromosomal and Genetic Variations (2 papers) and Microtubule and mitosis dynamics (2 papers). Duncan P. McHale collaborates with scholars based in United Kingdom, Pakistan and United States. Duncan P. McHale's co-authors include C. Geoffrey Woods, Hussain Jafri, Gulshan Karbani, Emma Roberts, Kelly Springell, Adeline K. Nicholas, Frank Reimann, Lihadh Al‐Gazali, Yasmin Raashid and Fiona M. Gribble and has published in prestigious journals such as Nature, Nature Genetics and The American Journal of Human Genetics.

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 — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Duncan P. McHale United Kingdom	9	1.0k	641	526	305	242	11	1.8k
Gregory R. Stewart United States	24	1.1k 1.1×	815 1.3×	1.0k 2.0×	160 0.5×	181 0.7×	36	2.2k
Matthias Sausbier Germany	28	1.6k 1.5×	534 0.8×	701 1.3×	205 0.7×	95 0.4×	40	2.5k
Berta González Spain	33	883 0.8×	435 0.7×	676 1.3×	1.5k 4.8×	100 0.4×	90	3.1k
Jisook Moon South Korea	23	876 0.8×	195 0.3×	522 1.0×	106 0.3×	287 1.2×	52	1.8k
Pascal E. Sanchez United States	14	581 0.6×	740 1.2×	595 1.1×	274 0.9×	191 0.8×	16	1.8k
Hitoe Nishino Japan	22	404 0.4×	159 0.2×	582 1.1×	152 0.5×	125 0.5×	67	2.1k
Marianna Storto Italy	29	1.2k 1.2×	457 0.7×	1.3k 2.4×	326 1.1×	232 1.0×	60	2.5k
Hideki Hida Japan	29	879 0.8×	212 0.3×	811 1.5×	498 1.6×	76 0.3×	81	2.2k
Loes H. Schrama Netherlands	24	1.0k 1.0×	242 0.4×	1.3k 2.4×	158 0.5×	114 0.5×	54	2.2k
Philippe G. Vallet Switzerland	23	636 0.6×	634 1.0×	466 0.9×	340 1.1×	32 0.1×	48	1.7k

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

1.

Wood, Linda S., Eve H. Pickering, Duncan P. McHale, & Bryan Dechairo. (2007). Association between neprilysin polymorphisms and sporadic Alzheimer's disease. Neuroscience Letters. 427(2). 103–106. 21 indexed citations

2.

Cox, James J., Frank Reimann, Adeline K. Nicholas, et al.. (2006). An SCN9A channelopathy causes congenital inability to experience pain. Nature. 444(7121). 894–898. 1094 indexed citations breakdown →

3.

Curtis, Andrew R.J., Christopher M. Morris, Laurence A. Bindoff, et al.. (2001). Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease. Nature Genetics. 28(4). 350–354. 386 indexed citations

4.

McHale, Duncan P., Simon J Mitchell, Sarah Bundey, et al.. (1999). A Gene for Autosomal Recessive Symmetrical Spastic Cerebral Palsy Maps to Chromosome 2q24-25. The American Journal of Human Genetics. 64(2). 526–532. 37 indexed citations

5.

Roberts, Emma, Andrew P. Jackson, Yasmin Abdul Rashid, et al.. (1999). The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1–13.2. European Journal of Human Genetics. 7(7). 815–820. 79 indexed citations

6.

Mitchell, Simon J., Duncan P. McHale, David A. Campbell, et al.. (1998). A Syndrome of Severe Mental Retardation, Spasticity, and Tapetoretinal Degeneration Linked to Chromosome 15q24. The American Journal of Human Genetics. 62(5). 1070–1076. 14 indexed citations

7.

Moynihan, Leanne, Sarah Bundey, Duncan P. McHale, et al.. (1998). Autozygosity Mapping, to Chromosome 11q25, of a Rare Autosomal Recessive Syndrome Causing Histiocytosis, Joint Contractures, and Sensorineural Deafness. The American Journal of Human Genetics. 62(5). 1123–1128. 27 indexed citations

8.

Jackson, Andrew P., Duncan P. McHale, David A. Campbell, et al.. (1998). Primary Autosomal Recessive Microcephaly (MCPH1) Maps to Chromosome 8p22-pter. The American Journal of Human Genetics. 63(2). 541–546. 117 indexed citations

9.

Campbell, David A., Duncan P. McHale, Kathryn Brown, et al.. (1997). A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.. Journal of Medical Genetics. 34(12). 1015–1017. 31 indexed citations

10.

Whittock, Neil V., et al.. (1996). Mutation analysis. Journal of Medical Genetics. 33(Suppl 1). S52–S58. 1 indexed citations

11.

McHale, Duncan P., et al.. (1996). Further evidence of genetic heterogeneity in hereditary hydronephrosis. Clinical Genetics. 50(6). 491–493. 4 indexed citations

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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