Mark Houseman

1.2k total citations
7 papers, 324 citations indexed

About

Mark Houseman is a scholar working on Sensory Systems, Molecular Biology and Neurology. According to data from OpenAlex, Mark Houseman has authored 7 papers receiving a total of 324 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Sensory Systems, 6 papers in Molecular Biology and 2 papers in Neurology. Recurrent topics in Mark Houseman's work include Hearing, Cochlea, Tinnitus, Genetics (7 papers), Connexins and lens biology (4 papers) and RNA regulation and disease (3 papers). Mark Houseman is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (7 papers), Connexins and lens biology (4 papers) and RNA regulation and disease (3 papers). Mark Houseman collaborates with scholars based in United Kingdom, Australia and United Arab Emirates. Mark Houseman's co-authors include David P. Kelsell, Wei‐Li Di, R F Mueller, Nicholas Lench, Graham R. Taylor, Valerie Newton, Leanne Moynihan, H Dahl, William Reardon and Lucy Ellis and has published in prestigious journals such as The American Journal of Human Genetics, British Journal of Dermatology and Journal of Medical Genetics.

In The Last Decade

Mark Houseman

7 papers receiving 317 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mark Houseman United Kingdom	7	233	218	69	69	55	7	324
Ana Carla Batissoco Brazil	12	169 0.7×	246 1.1×	39 0.6×	76 1.1×	66 1.2×	21	333
Niloofar Bazazzadegan Iran	11	255 1.1×	317 1.5×	78 1.1×	154 2.2×	27 0.5×	26	407
Liang Zong China	12	302 1.3×	337 1.5×	32 0.5×	108 1.6×	103 1.9×	23	468
Dilip Deshmukh United States	5	218 0.9×	257 1.2×	18 0.3×	83 1.2×	45 0.8×	6	331
Marta Gandía Spain	7	147 0.6×	197 0.9×	33 0.5×	100 1.4×	27 0.5×	8	277
Sanaz Arzhangi Iran	10	245 1.1×	315 1.4×	64 0.9×	146 2.1×	29 0.5×	25	384
Marzieh Mohseni Iran	13	259 1.1×	223 1.0×	53 0.8×	125 1.8×	27 0.5×	37	470
Araceli Álvarez Spain	4	381 1.6×	474 2.2×	122 1.8×	129 1.9×	111 2.0×	5	559
Kris Flothmann Belgium	8	237 1.0×	233 1.1×	41 0.6×	90 1.3×	77 1.4×	8	409
Nooshin Nikzat Iran	9	122 0.5×	178 0.8×	33 0.5×	93 1.3×	26 0.5×	16	243

Countries citing papers authored by Mark Houseman

Since Specialization

Citations

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

Fields of papers citing papers by Mark Houseman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark Houseman

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

All Works

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

1.

Kelsell, David P., Wei‐Li Di, & Mark Houseman. (2001). Connexin Mutations in Skin Disease and Hearing Loss. The American Journal of Human Genetics. 68(3). 559–568. 114 indexed citations

2.

Houseman, Mark, Lucy Ellis, Alistair T. Pagnamenta, et al.. (2001). Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss. Journal of Medical Genetics. 38(1). 20–25. 75 indexed citations

3.

Jackson, Andrew P., et al.. (2000). A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23–q31. European Journal of Human Genetics. 8(12). 991–993. 19 indexed citations

4.

Ishida‐Yamamoto, Akemi, David P. Kelsell, John Common, et al.. (2000). A case of erythrokeratoderma variabilis without mutations in connexin 31. British Journal of Dermatology. 143(6). 1283–1287. 18 indexed citations

5.

Mueller, R F, Anna Middleton, Mark Houseman, et al.. (1999). Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations — molecular and audiological findings. International Journal of Pediatric Otorhinolaryngology. 50(1). 3–13. 51 indexed citations

6.

Moynihan, Leanne, Mark Houseman, Valerie Newton, Robert F. Mueller, & Nicholas Lench. (1999). DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25–qter. European Journal of Human Genetics. 7(2). 243–246. 16 indexed citations

7.

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

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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