Mark J. McCabe

1.6k total citations
22 papers, 707 citations indexed

About

Mark J. McCabe is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Mark J. McCabe has authored 22 papers receiving a total of 707 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Mark J. McCabe's work include Growth Hormone and Insulin-like Growth Factors (6 papers), Genetic Syndromes and Imprinting (4 papers) and Hedgehog Signaling Pathway Studies (4 papers). Mark J. McCabe is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (6 papers), Genetic Syndromes and Imprinting (4 papers) and Hedgehog Signaling Pathway Studies (4 papers). Mark J. McCabe collaborates with scholars based in United Kingdom, Australia and United States. Mark J. McCabe's co-authors include Mehul Dattani, Kyriaki S. Alatzoglou, Louise Gregory, Mark J. Cowley, Peter G. Stanton, Carles Gaston‐Massuet, Rodrigo Bancalari, Marcel E. Dinger, Juan Pedro Martı́nez-Barberá and Kristina Warton and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Endocrinology and Genome biology.

In The Last Decade

Mark J. McCabe

21 papers receiving 693 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark J. McCabe United Kingdom 16 331 259 234 103 100 22 707
Valère Cacheux France 10 415 1.3× 417 1.6× 244 1.0× 52 0.5× 53 0.5× 12 847
Jesse J. Savage United States 12 301 0.9× 213 0.8× 281 1.2× 30 0.3× 52 0.5× 23 658
Sophie Vallette-Kasic France 16 401 1.2× 264 1.0× 854 3.6× 56 0.5× 104 1.0× 23 1.2k
Bartłomiej Budny Poland 14 376 1.1× 396 1.5× 209 0.9× 31 0.3× 30 0.3× 45 706
Kyriaki S. Alatzoglou United Kingdom 15 334 1.0× 327 1.3× 491 2.1× 54 0.5× 25 0.3× 23 821
Ajith Kumar United Kingdom 14 273 0.8× 227 0.9× 392 1.7× 32 0.3× 184 1.8× 37 887
Louise Gregory United Kingdom 14 224 0.7× 171 0.7× 258 1.1× 35 0.3× 26 0.3× 25 520
Rodger Palmer United Kingdom 13 397 1.2× 494 1.9× 146 0.6× 21 0.2× 51 0.5× 20 915
Soo‐Mi Park United Kingdom 15 464 1.4× 258 1.0× 147 0.6× 13 0.1× 79 0.8× 39 794
Vassos Neocleous Cyprus 15 444 1.3× 261 1.0× 223 1.0× 73 0.7× 12 0.1× 61 728

Countries citing papers authored by Mark J. McCabe

Since Specialization
Citations

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

Fields of papers citing papers by Mark J. McCabe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark J. McCabe

This figure shows the co-authorship network connecting the top 25 collaborators of Mark J. McCabe. A scholar is included among the top collaborators of Mark J. McCabe 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 J. McCabe. Mark J. McCabe 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.
Gayevskiy, Velimir, Ryan L. Davis, Marie Wong, et al.. (2023). Introme accurately predicts the impact of coding and noncoding variants on gene splicing, with clinical applications. Genome biology. 24(1). 118–118. 10 indexed citations
2.
Gregory, Louise, Péter Gergics, Hironori Bando, et al.. (2021). The phenotypic spectrum associated with OTX2 mutations in humans. European Journal of Endocrinology. 185(1). 121–135. 20 indexed citations
3.
Warton, Kristina, et al.. (2017). Evaluation of Streck BCT and PAXgene Stabilised Blood Collection Tubes for Cell-Free Circulating DNA Studies in Plasma. Molecular Diagnosis & Therapy. 21(5). 563–570. 60 indexed citations
4.
Sousa, Sunita M C De, Mark J. McCabe, Kathy H. C. Wu, et al.. (2017). Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumours. European Journal of Endocrinology. 176(5). 635–644. 26 indexed citations
5.
Mallawaarachchi, Amali, Yvonne Hort, Mark J. Cowley, et al.. (2016). Whole-genome sequencing overcomes pseudogene homology to diagnose autosomal dominant polycystic kidney disease. European Journal of Human Genetics. 24(11). 1584–1590. 58 indexed citations
6.
McCabe, Mark J., Gerard A. Tarulli, Geraldine Laven‐Law, et al.. (2016). Gonadotropin suppression in men leads to a reduction in claudin-11 at the Sertoli cell tight junction. Human Reproduction. 31(4). 875–886. 18 indexed citations
7.
Gregory, Louise, Kyriaki S. Alatzoglou, Mark J. McCabe, et al.. (2016). Partial Loss of Function of the GHRH Receptor Leads to Mild Growth Hormone Deficiency. The Journal of Clinical Endocrinology & Metabolism. 101(10). 3608–3615. 5 indexed citations
8.
Gregory, Louise, Khadija Nuzhat Humayun, James Turton, et al.. (2015). Novel Lethal Form of Congenital Hypopituitarism Associated With the First Recessive LHX4 Mutation. eCommons - AKU (Aga Khan University). 3 indexed citations
9.
Gregory, Louise, Khadija Nuzhat Humayun, James Turton, et al.. (2015). Novel Lethal Form of Congenital Hypopituitarism Associated With the First RecessiveLHX4Mutation. The Journal of Clinical Endocrinology & Metabolism. 100(6). 2158–2164. 26 indexed citations
10.
McCabe, Mark J., Youli Hu, Louise Gregory, et al.. (2015). Novel application of luciferase assay for the in vitro functional assessment of KAL1 variants in three females with septo-optic dysplasia (SOD). Molecular and Cellular Endocrinology. 417. 63–72. 14 indexed citations
11.
McCabe, Mark J. & Mehul Dattani. (2014). Genetic aspects of hypothalamic and pituitary gland development. Handbook of clinical neurology. 124. 3–15. 23 indexed citations
12.
McCabe, Mark J., Rodrigo Bancalari, & Mehul Dattani. (2014). Diagnosis and evaluation of hypogonadism.. PubMed. 11 Suppl 2. 214–29. 8 indexed citations
13.
Gregory, Louise, Carles Gaston‐Massuet, Cynthia L. Andoniadou, et al.. (2014). The role of the sonic hedgehog signalling pathway in patients with midline defects and congenital hypopituitarism. Clinical Endocrinology. 82(5). 728–738. 27 indexed citations
14.
McCabe, Mark J., Carles Gaston‐Massuet, Louise Gregory, et al.. (2013). Variations inPROKR2, But NotPROK2, Are Associated With Hypopituitarism and Septo-optic Dysplasia. The Journal of Clinical Endocrinology & Metabolism. 98(3). E547–E557. 47 indexed citations
15.
McCabe, Mark J., et al.. (2012). Androgen Initiates Sertoli Cell Tight Junction Formation in the Hypogonadal (hpg) Mouse1. Biology of Reproduction. 87(2). 38–38. 41 indexed citations
16.
Bancalari, Rodrigo, Louise Gregory, Mark J. McCabe, & Mehul Dattani. (2012). Pituitary Gland Development: An Update. Endocrine development. 23. 1–15. 41 indexed citations
17.
McCabe, Mark J., Carles Gaston‐Massuet, Vaitsa Tziaferi, et al.. (2011). Mutations in the gene encoding the fibroblast growth factor 8 (FGF8) are associated with complex midline defects including recessive holoprosencephaly and hypothalamo-pituitary dysfunction. Endocrine Abstracts. 25.
18.
McCabe, Mark J., Carles Gaston‐Massuet, Vaitsa Tziaferi, et al.. (2011). NovelFGF8Mutations Associated with Recessive Holoprosencephaly, Craniofacial Defects, and Hypothalamo-Pituitary Dysfunction. The Journal of Clinical Endocrinology & Metabolism. 96(10). E1709–E1718. 97 indexed citations
19.
McCabe, Mark J., Kyriaki S. Alatzoglou, & Mehul Dattani. (2011). Septo-optic dysplasia and other midline defects: The role of transcription factors: HESX1 and beyond. Best Practice & Research Clinical Endocrinology & Metabolism. 25(1). 115–124. 79 indexed citations
20.
McCabe, Mark J., Gerard A. Tarulli, Sarah J. Meachem, et al.. (2010). Gonadotropins Regulate Rat Testicular Tight Junctions in Vivo. Endocrinology. 151(6). 2911–2922. 45 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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