Howard Martin

2.4k total citations
32 papers, 1.3k citations indexed

About

Howard Martin is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Howard Martin has authored 32 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 14 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Howard Martin's work include Connective tissue disorders research (10 papers), Sexual Differentiation and Disorders (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Howard Martin is often cited by papers focused on Connective tissue disorders research (10 papers), Sexual Differentiation and Disorders (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Howard Martin collaborates with scholars based in United Kingdom, United States and Australia. Howard Martin's co-authors include Ieuan A. Hughes, J. Ross Hawkins, Lionel Willatt, A.D. Tait, Naoto Shimura, S. Faisal Ahmed, Anna Wai-Fun Cheng, Charles Shaw‐Smith, Helen V. Firth and Ursula Goodenough and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Genetics.

In The Last Decade

Howard Martin

29 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Howard Martin United Kingdom 16 735 727 240 109 103 32 1.3k
Michela Barbaro Sweden 22 596 0.8× 885 1.2× 298 1.2× 50 0.5× 52 0.5× 47 1.3k
Soazik P. Jamin France 21 731 1.0× 1.2k 1.7× 133 0.6× 21 0.2× 101 1.0× 29 2.5k
Stavit A. Shalev Israel 29 709 1.0× 1.8k 2.5× 206 0.9× 21 0.2× 114 1.1× 88 2.6k
Virpi Töhönen Sweden 19 445 0.6× 980 1.3× 46 0.2× 47 0.4× 120 1.2× 32 1.4k
Elizabeth Roeder United States 21 972 1.3× 1.2k 1.6× 90 0.4× 158 1.4× 216 2.1× 37 1.9k
Makoto Matsuyama Japan 22 481 0.7× 1.2k 1.6× 62 0.3× 42 0.4× 173 1.7× 58 1.8k
Patricia G. Wheeler United States 22 400 0.5× 529 0.7× 49 0.2× 45 0.4× 151 1.5× 41 1.1k
Laura Milne United Kingdom 17 223 0.3× 564 0.8× 122 0.5× 29 0.3× 114 1.1× 27 1.3k
Anna Lindstrand Sweden 22 827 1.1× 882 1.2× 29 0.1× 140 1.3× 89 0.9× 84 1.5k
Dawn E. Watkins‐Chow United States 17 237 0.3× 648 0.9× 125 0.5× 45 0.4× 63 0.6× 37 1.1k

Countries citing papers authored by Howard Martin

Since Specialization
Citations

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

Fields of papers citing papers by Howard Martin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Howard Martin

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

All Works

20 of 20 papers shown
1.
Cheng, Kevin, et al.. (2025). Myopia progression in children with Stickler syndrome: a longitudinal cohort study. Journal of American Association for Pediatric Ophthalmology and Strabismus. 29(3). 104206–104206. 1 indexed citations
2.
Khatib, Tasneem, Giovanni Montesano, Howard Martin, et al.. (2024). Peripapillary Hyperreflective Ovoid Mass-Like Structures in Stickler Syndrome. Ophthalmology Retina. 8(10). 1013–1020. 1 indexed citations
3.
Martin, Howard, Allan J. Richards, Annie McNinch, et al.. (2024). Retinal detachment in Type IX collagen recessive Stickler syndrome. Eye. 39(1). 133–138.
4.
Snead, Martin P., et al.. (2024). Pathobiology of the crystalline lens in Stickler syndrome. Progress in Retinal and Eye Research. 103. 101304–101304.
5.
Wang, Aijing, Howard Martin, Allan J. Richards, et al.. (2023). Legg-Calve-Perthes’ disease: an opportunity to prevent blindness?. Archives of Disease in Childhood. 108(10). 789–791.
6.
Maletić‐Savatić, Mirjana, et al.. (2022). Spatial analysis of drug absorption, distribution, metabolism, and toxicology using mass spectrometry imaging. Biochemical Pharmacology. 201. 115080–115080. 41 indexed citations
7.
Snead, Martin P., Allan J. Richards, Annie McNinch, et al.. (2021). Stickler syndrome – lessons from a national cohort. Eye. 36(10). 1966–1972. 16 indexed citations
8.
Brown, Nicholas M., Mark Reacher, Iain Roddick, et al.. (2019). An outbreak of meticillin-resistant Staphylococcus aureus colonization in a neonatal intensive care unit: use of a case–control study to investigate and control it and lessons learnt. Journal of Hospital Infection. 103(1). 35–43. 10 indexed citations
9.
Martin, Howard, et al.. (2015). P024: Evaluating the use and reporting of minority variants in HIV genotypic testing using ultra-deep sequencing. Journal of the International AIDS Society. 18(3 (Suppl 2)). 9 indexed citations
10.
Wang, Ming, Leire Escudero‐Ibarz, Sarah Moody, et al.. (2015). Somatic Mutation Screening Using Archival Formalin-Fixed, Paraffin-Embedded Tissues by Fluidigm Multiplex PCR and Illumina Sequencing. Journal of Molecular Diagnostics. 17(5). 521–532. 18 indexed citations
11.
Plumb, Lucy, Matko Marlais, Agnieszka Bierżyńska, et al.. (2014). Unilateral hypoplastic kidney - a novel highly penetrant feature of familial juvenile hyperuricaemic nephropathy. BMC Nephrology. 15(1). 76–76. 3 indexed citations
12.
Richards, Allan J., Annie McNinch, Howard Martin, et al.. (2010). Stickler syndrome and the vitreous phenotype: mutations in COL2A1 and COL11A1. Human Mutation. 31(6). E1461–E1471. 99 indexed citations
13.
Zahir, Farah, Helen V. Firth, Ágnes Baross, et al.. (2007). Novel deletions of 14q11.2 associated with developmental delay, cognitive impairment and similar minor anomalies in three children. Journal of Medical Genetics. 44(9). 556–561. 63 indexed citations
14.
Shaw‐Smith, Charles, Alan Pittman, Lionel Willatt, et al.. (2006). Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability. Nature Genetics. 38(9). 1032–1037. 258 indexed citations
15.
Willatt, Lionel, James J. Cox, John Barber, et al.. (2005). 3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome. The American Journal of Human Genetics. 77(1). 154–160. 166 indexed citations
16.
Hughes, Ieuan A., Howard Martin, & Jarmo Jääskeläinen. (2005). Genetic mechanisms of fetal male undermasculinization: A background to the role of endocrine disruptors. Environmental Research. 100(1). 44–49. 5 indexed citations
17.
Hannema, Sabine E, Ian Scott, Howard Martin, et al.. (2004). Residual Activity of Mutant Androgen Receptors Explains Wolffian Duct Development in the Complete Androgen Insensitivity Syndrome. The Journal of Clinical Endocrinology & Metabolism. 89(11). 5815–5822. 52 indexed citations
18.
Hughes, I A, Howard Martin, Jarmo Jääskeläinen, & Carlo L. Acerini. (2003). Nuclear receptor action involved with sex differentiation. Pure and Applied Chemistry. 75(11-12). 1771–1784. 3 indexed citations
19.
Hughes, Ieuan A., Han N. Lim, Howard Martin, et al.. (2001). Developmental aspects of androgen action. Molecular and Cellular Endocrinology. 185(1-2). 33–41. 21 indexed citations
20.
Ahmed, S. Faisal, Anna Wai-Fun Cheng, J. Ross Hawkins, et al.. (2000). Phenotypic Features, Androgen Receptor Binding, and Mutational Analysis in 278 Clinical Cases Reported as Androgen Insensitivity Syndrome1. The Journal of Clinical Endocrinology & Metabolism. 85(2). 658–665. 230 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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