H G Harley

4.1k total citations
35 papers, 1.0k citations indexed

About

H G Harley is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, H G Harley has authored 35 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Cellular and Molecular Neuroscience, 23 papers in Molecular Biology and 7 papers in Neurology. Recurrent topics in H G Harley's work include Genetic Neurodegenerative Diseases (24 papers), Mitochondrial Function and Pathology (13 papers) and Parkinson's Disease Mechanisms and Treatments (5 papers). H G Harley is often cited by papers focused on Genetic Neurodegenerative Diseases (24 papers), Mitochondrial Function and Pathology (13 papers) and Parkinson's Disease Mechanisms and Treatments (5 papers). H G Harley collaborates with scholars based in United Kingdom, United States and Germany. H G Harley's co-authors include Peter S. Harper, Duncan J. Shaw, William Reardon, J. David Brook, S.A. Rundle, Steve Crow, J Myring, K.V. Walsh, D J Shaw and Maria Anvret and has published in prestigious journals such as The Lancet, Nucleic Acids Research and The American Journal of Human Genetics.

In The Last Decade

H G Harley

35 papers receiving 998 citations

Peers

Countries citing papers authored by H G Harley

Since Specialization

Citations

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

Fields of papers citing papers by H G Harley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H G Harley. 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 H G Harley. The network helps show where H G Harley may publish in the future.

Co-authorship network of co-authors of H G Harley

This figure shows the co-authorship network connecting the top 25 collaborators of H G Harley. A scholar is included among the top collaborators of H G Harley 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 H G Harley. H G Harley 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	PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafness 1998 ·Neuromuscular Disorders ·Margaret Phillips, Mark T. Rogers, Rebecca A. Barnetson, (unknown), H G Harley, J Myring, (unknown), C M Wiles, Peter S. Harper	24
2	Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy. 1994 ·PubMed ·Tetsuo Ashizawa, Maria Anvret, Montserrat Baiget, (unknown), (unknown), Ana María Cobo, Bruno Dallapiccola, (unknown), Ulla Grandell, H G Harley	99
3	Genomic organization and transcriptional units at the myotonic dystrophy locus 1993 ·Genomics ·Duncan J. Shaw, Mila E. McCurrach, S.A. Rundle, H G Harley, (unknown), (unknown), Jean‐Paul Thirion, Marion Hamshere, Alan Buckler, Peter S. Harper, David E. Housman, J. David Brook	56
4	The DM mutation; diagnostic applications in the Finnish population 1993 ·Clinical Genetics ·Pekka Nokelainen, Peggy Shelbourne, Duncan Shaw, J. David Brook, H G Harley, Keith Johnson, Hannu Somer, M L Savontaus, Leena Peltonen	3
5	Cataract and myotonic dystrophy: the role of molecular diagnosis. 1993 ·British Journal of Ophthalmology ·William Reardon, J. MacMillan, J Myring, H G Harley, S.A. Rundle, (unknown), Peter S. Harper, D J Shaw	13
6	Reply to Goodship et al. 1992 ·The American Journal of Human Genetics ·Manuela C. Koch, T. Grimm, H G Harley, Peter S. Harper	2
7	Unstable DNA sequence in myotonic dystrophy 1992 ·The Lancet ·H G Harley, S.A. Rundle, William Reardon, J Myring, Steve Crow, Peter S. Harper, (unknown), J. David Brook	143
8	Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeat 1992 ·Human Molecular Genetics ·Steve Crow, H G Harley, J. David Brook, S.A. Rundle, Duncan J. Shaw	8
9	Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q 1992 ·Genomics ·Gert Jansen, Pieter J. de Jong, Chris T. Amemiya, Charalampos Aslanidis, Duncan J. Shaw, H G Harley, J. David Brook, (unknown), Robert G. Korneluk, Catherine Tsilfidis, Gary Shutler, Rosella Hermens, (unknown), Hubert J.M. Smeets, Bé Wieringa	30
10	Radiation-reduced hybrids for the myotonic dystrophy locus 1992 ·Genomics ·J. David Brook, Boris V. Zemelman, (unknown), Michael J. Siciliano, Steve Crow, H G Harley, S.A. Rundle, Jessica L. Buxton, Keith Johnson, J. W. Almond, David E. Housman, Duncan J. Shaw	16
11	Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19 1992 ·Cytogenetic and Genome Research ·Anna L. Mitchell, A. Bale, (unknown), Dolph L. Hatfield, H G Harley, S.A. Rundle, Yao Fan, Yoshimitsu Fukushima, T.B. Shows, O. Wesley McBride	6
12	Molecular analysis for the myotonic dystrophy mutation in neuromuscular disorders 1992 ·Neuromuscular Disorders ·J. MacMillan, J Myring, H G Harley, William Reardon, Peter S. Harper, D J Shaw	1
13	Human glandular kallikrein genes: Genetic and physical mapping of the KLK1 locus using a highly polymorphic microsatellite PCR marker 1991 ·Genomics ·Robert I. Richards, Katherine Holman, Yang Shen, H.M. Kozman, H G Harley, J. David Brook, Duncan Shaw	23
14	Localisation of the myotonic dystrophy locus to 19q13.2?19q13.3 and its relationship to twelve polymorphic loci on 19q 1991 ·Human Genetics ·H G Harley, K.V. Walsh, S.A. Rundle, J. David Brook, M. Sarfarazi, Manuela C. Koch, (unknown), Peter S. Harper, Duncan J. Shaw	26
15	The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessments 1991 ·Human Genetics ·J. David Brook, Samantha J.L. Knight, Susan Roberts, H G Harley, K.V. Walsh, S.A. Rundle, (unknown), Manuela C. Koch, Nava Epstein, Bé Wieringa, (unknown), H.J.M. Smeets, (unknown), Michael J. Siciliano, D K Palmer, J S Miles, C. Roland Wolf, Christa Fonatsch, Duncan J. Shaw	12
16	A polymorphic DNA clone which maps to 19q13.2 - 19qter (D19S62) 1990 ·Nucleic Acids Research ·J. David Brook, K.V. Walsh, H G Harley, S.A. Rundle, Duncan J. Shaw	5
17	Genetic and physical mapping and population studies of a fibronectin receptor β-subunit-like sequence on human chromosome 19 1990 ·Genomics ·L. Giuffra, Peter Lichter, (unknown), James L. Kennedy, A.J. Pakstis, Jeffrey Rogers, Judith R. Kidd, H G Harley, Trefor Jenkins, David C. Ward, Kenneth K. Kídd	6
18	Paramyotonia congenita and myotonic dystrophy are not allelic disorders 1989 ·Cytogenetic and Genome Research ·Manuela C. Koch, H G Harley, T. Grimm, M. Sarfarazi, Berndt Müller, Barbara Zoll, Peter S. Harper	1
19	Long-range restriction map of a region of human chromosome 19 containing the apolipoprotein genes, a CLL-associated translocation breakpoint, and two polymorphic MluI sites 1989 ·Human Genetics ·D J Shaw, H G Harley, J. David Brook, Timothy W. McKeithan	22
20	Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19 1989 ·Human Genetics ·Manuela C. Koch, H G Harley, M. Sarfarazi, K. Bender, (unknown), Barbara Zoll, Peter S. Harper	5

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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