Kenneth McElreavey

1.3k total citations
30 papers, 555 citations indexed

About

Kenneth McElreavey is a scholar working on Molecular Biology, Genetics and Urology. According to data from OpenAlex, Kenneth McElreavey has authored 30 papers receiving a total of 555 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 20 papers in Genetics and 7 papers in Urology. Recurrent topics in Kenneth McElreavey's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (16 papers), Sexual Differentiation and Disorders (15 papers) and Urological Disorders and Treatments (7 papers). Kenneth McElreavey is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (16 papers), Sexual Differentiation and Disorders (15 papers) and Urological Disorders and Treatments (7 papers). Kenneth McElreavey collaborates with scholars based in France, Tunisia and Egypt. Kenneth McElreavey's co-authors include Anu Bashamboo, W.H. Irwin McLean, Debbie Montjean, Moncef Benkhalifa, P. Cohen-Bacrie, Célia Ravel, Isabelle Berthaut, Sandra Rojo, Kayo Kurahashi and Vivian J. Bardwell and has published in prestigious journals such as PLoS ONE, Nature Structural & Molecular Biology and Gene.

In The Last Decade

Kenneth McElreavey

29 papers receiving 532 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kenneth McElreavey France 12 309 221 136 114 101 30 555
Ludmila Ruban United Kingdom 13 606 2.0× 128 0.6× 100 0.7× 62 0.5× 214 2.1× 19 797
Hiroyuki Naora Japan 9 209 0.7× 88 0.4× 73 0.5× 35 0.3× 92 0.9× 19 401
Anna Latos‐Bieleńska Poland 15 501 1.6× 504 2.3× 91 0.7× 17 0.1× 117 1.2× 50 895
Fernándo Rodríguez Chile 12 218 0.7× 119 0.5× 101 0.7× 46 0.4× 37 0.4× 38 516
Adriana Rojas Colombia 14 360 1.2× 106 0.5× 33 0.2× 45 0.4× 52 0.5× 40 540
Navid Almadani Iran 14 352 1.1× 233 1.1× 213 1.6× 113 1.0× 56 0.6× 45 702
Fiona L. Cousins Australia 18 140 0.5× 91 0.4× 725 5.3× 42 0.4× 124 1.2× 35 1.1k
Marco Casasco Italy 13 159 0.5× 79 0.4× 25 0.2× 48 0.4× 76 0.8× 44 503
Toru Arase Japan 13 204 0.7× 82 0.4× 407 3.0× 70 0.6× 79 0.8× 18 829
Marilyn Lamm United States 17 758 2.5× 181 0.8× 94 0.7× 21 0.2× 73 0.7× 27 986

Countries citing papers authored by Kenneth McElreavey

Since Specialization
Citations

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

Fields of papers citing papers by Kenneth McElreavey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kenneth McElreavey

This figure shows the co-authorship network connecting the top 25 collaborators of Kenneth McElreavey. A scholar is included among the top collaborators of Kenneth McElreavey 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 Kenneth McElreavey. Kenneth McElreavey 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.
Askari, Masomeh, et al.. (2025). Clinical and genetic diagnosis of first cohort of differences of sexual development in the Iranian population. Journal of Pediatric Endocrinology and Metabolism. 38(3). 279–287.
2.
Kamaoui, Imane, et al.. (2022). Novel homozygous inactivating mutation in the luteinizing hormone receptor gene (LHCGR) associated with 46, XY DSD in a Moroccan family. Journal of Pediatric Endocrinology and Metabolism. 35(9). 1215–1221. 1 indexed citations
3.
Turki, Z., Sahar Elouej, Yosra Bouyacoub, et al.. (2021). Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism. Frontiers in Genetics. 12. 665174–665174. 3 indexed citations
4.
Kammoun, Molka, et al.. (2021). Further report of MEDS syndrome: Clinical and molecular delineation of a new Tunisian case. European Journal of Medical Genetics. 64(9). 104285–104285. 5 indexed citations
5.
Globa, Evgenia, et al.. (2020). Atypical Clinical Presentation of Persistent Müllerian Duct Syndrome in Siblings. Sexual Development. 14(1-6). 27–32. 2 indexed citations
6.
Askari, Masomeh, et al.. (2020). A missense mutation in NR5A1 causing female to male sex reversal: A case report. Andrologia. 52(6). e13585–e13585. 7 indexed citations
7.
Amouri, Ahlem, Saloua Makni, Lilia Romdhane, et al.. (2019). Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro‐oculo‐facio‐skeletal syndrome. Molecular Genetics & Genomic Medicine. 7(7). e00694–e00694. 3 indexed citations
8.
Askari, Masomeh, Dor Mohammad Kordi-Tamandani, Navid Almadani, Kenneth McElreavey, & Mehdi Totonchi. (2019). Identification of a homozygous GFPT2 variant in a family with asthenozoospermia. Gene. 699. 16–23. 13 indexed citations
9.
Mazen, Inas, et al.. (2018). A Homozygous Missense Mutation in <b><i>FANCA</i></b> Gene in a 46,XY Female with Gonadal Dysgenesis. Sexual Development. 12(5). 239–243. 2 indexed citations
10.
Mottet, Nicolas, Christelle Cabrol, Francine Arbez‐Gindre, et al.. (2018). Autopsy findings of ectodermal dysplasia and sex development disorder in a fetus with 19q12q13 microdeletion. European Journal of Medical Genetics. 62(9). 103539–103539. 2 indexed citations
11.
Nagara, Majdi, Gregory Papagregoriou, Zied Landoulsi, et al.. (2017). Distal renal tubular acidosis in a Libyan patient: Evidence for digenic inheritance. European Journal of Medical Genetics. 61(1). 1–7. 7 indexed citations
12.
Rekaya, Mariem Ben, Olfa Messaoud, M. Jones, et al.. (2017). Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis. Journal of Dermatological Science. 89(2). 172–180. 15 indexed citations
13.
Winter, Sarah, et al.. (2016). Constitutional delay of puberty: presentation and inheritance pattern in 48 familial cases. BMC Pediatrics. 16(1). 37–37. 10 indexed citations
14.
Murphy, Mark W., John K. Lee, Sandra Rojo, et al.. (2015). An ancient protein-DNA interaction underlying metazoan sex determination. Nature Structural & Molecular Biology. 22(6). 442–451. 82 indexed citations
15.
Bonnet, Crystel, Malek Louha, Yosra Bouyacoub, et al.. (2014). Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness. PLoS ONE. 9(6). e99797–e99797. 21 indexed citations
16.
Piard, Juliette, Brigitte Mignot, Francine Arbez‐Gindre, et al.. (2014). Severe sex differentiation disorder in a boy with a 3.8 Mb 10q25.3–q26.12 microdeletion encompassing EMX2. American Journal of Medical Genetics Part A. 164(10). 2618–2622. 32 indexed citations
17.
Montjean, Debbie, Célia Ravel, Moncef Benkhalifa, et al.. (2013). Methylation changes in mature sperm deoxyribonucleic acid from oligozoospermic men: assessment of genetic variants and assisted reproductive technology outcome. Fertility and Sterility. 100(5). 1241–1247.e2. 63 indexed citations
18.
Song, Manshu, et al.. (2011). Semen quality analysis of military personnel from six geographical areas of the People’s Republic of China. Fertility and Sterility. 95(6). 2018–2023.e3. 29 indexed citations
19.
Montjean, Debbie, Moncef Benkhalifa, Lionel Dessolle, et al.. (2010). Polymorphisms in MTHFR and MTRR genes associated with blood plasma homocysteine concentration and sperm counts. Fertility and Sterility. 95(2). 635–640. 36 indexed citations
20.
McElreavey, Kenneth, et al.. (1991). Isolation, culture and characterisation of fibroblast-like cells derived from the Wharton's jelly portion of human umbilical cord. Biochemical Society Transactions. 19(1). 29S–29S. 131 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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