Louise Gregory

1.3k total citations
25 papers, 520 citations indexed

About

Louise Gregory is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Louise Gregory has authored 25 papers receiving a total of 520 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Endocrinology, Diabetes and Metabolism and 10 papers in Genetics. Recurrent topics in Louise Gregory's work include Growth Hormone and Insulin-like Growth Factors (10 papers), Genetic Syndromes and Imprinting (6 papers) and Hedgehog Signaling Pathway Studies (4 papers). Louise Gregory is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (10 papers), Genetic Syndromes and Imprinting (6 papers) and Hedgehog Signaling Pathway Studies (4 papers). Louise Gregory collaborates with scholars based in United Kingdom, United States and Pakistan. Louise Gregory's co-authors include Mehul Dattani, Mark J. McCabe, Kyriaki S. Alatzoglou, Carles Gaston‐Massuet, Juan Pedro Martı́nez-Barberá, Rodrigo Bancalari, Nelly Pitteloud, Vaitsa Tziaferi, Pei‐San Tsai and Sally A. Camper and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, International Journal of Molecular Sciences and Clinical Chemistry.

In The Last Decade

Louise Gregory

22 papers receiving 507 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Louise Gregory United Kingdom 14 258 224 171 82 58 25 520
Péter Gergics Hungary 14 257 1.0× 209 0.9× 134 0.8× 90 1.1× 23 0.4× 29 501
James Turton United Kingdom 12 484 1.9× 290 1.3× 297 1.7× 96 1.2× 52 0.9× 15 710
Ameeta Mehta United Kingdom 10 461 1.8× 270 1.2× 270 1.6× 90 1.1× 42 0.7× 11 682
Kyriaki S. Alatzoglou United Kingdom 15 491 1.9× 334 1.5× 327 1.9× 114 1.4× 68 1.2× 23 821
Vassos Neocleous Cyprus 15 223 0.9× 444 2.0× 261 1.5× 62 0.8× 60 1.0× 61 728
Soo‐Mi Park United Kingdom 15 147 0.6× 464 2.1× 258 1.5× 74 0.9× 41 0.7× 39 794
Jesse J. Savage United States 12 281 1.1× 301 1.3× 213 1.2× 82 1.0× 92 1.6× 23 658
Lisa J. Cushman United States 9 193 0.7× 297 1.3× 229 1.3× 31 0.4× 36 0.6× 15 541
Johannes Weigel Germany 11 196 0.8× 279 1.2× 179 1.0× 42 0.5× 22 0.4× 15 512
Youn Hee Jee United States 13 147 0.6× 253 1.1× 173 1.0× 30 0.4× 14 0.2× 30 506

Countries citing papers authored by Louise Gregory

Since Specialization
Citations

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

Fields of papers citing papers by Louise Gregory

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Louise Gregory

This figure shows the co-authorship network connecting the top 25 collaborators of Louise Gregory. A scholar is included among the top collaborators of Louise Gregory 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 Louise Gregory. Louise Gregory 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.
Gregory, Louise, et al.. (2023). Identification of genetic variants and phenotypic characterization of a large cohort of patients with congenital hypopituitarism and related disorders. Genetics in Medicine. 25(9). 100881–100881. 12 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.
Hietamäki, Johanna, Louise Gregory, Kirsi Vaaralahti, et al.. (2020). Loss-of-Function Variants in TBC1D32 Underlie Syndromic Hypopituitarism. The Journal of Clinical Endocrinology & Metabolism. 105(6). 1748–1758. 18 indexed citations
4.
Alatzoglou, Kyriaki S., Louise Gregory, & Mehul Dattani. (2020). Development of the Pituitary Gland. Comprehensive physiology. 10(2). 389–413. 5 indexed citations
5.
Alatzoglou, Kyriaki S., Louise Gregory, & Mehul Dattani. (2020). Development of the Pituitary Gland. Comprehensive physiology. 10(2). 389–413. 40 indexed citations
6.
Cleal, Jane K., Kimberley D. Bruce, Hugh Thomas, et al.. (2019). Maternal Obesity during Pregnancy Alters Daily Activity and Feeding Cycles, and Hypothalamic Clock Gene Expression in Adult Male Mouse Offspring. International Journal of Molecular Sciences. 20(21). 5408–5408. 14 indexed citations
7.
Gregory, Louise, Sara K. Young, Hywel Williams, et al.. (2019). Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulation. EBioMedicine. 42. 470–480. 40 indexed citations
8.
Gregory, Louise, Wendy D. Jones, Helen Spoudeas, et al.. (2019). Mutations in MAGEL2 and L1CAM Are Associated With Congenital Hypopituitarism and Arthrogryposis. The Journal of Clinical Endocrinology & Metabolism. 104(12). 5737–5750. 3 indexed citations
9.
Gregory, Louise & Mehul Dattani. (2019). The Molecular Basis of Congenital Hypopituitarism and Related Disorders. The Journal of Clinical Endocrinology & Metabolism. 105(6). e2103–e2120. 36 indexed citations
10.
Fang, Qing, Anna Benedetti, Qianyi Ma, et al.. (2016). HESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype. Clinical Endocrinology. 85(3). 408–414. 22 indexed citations
11.
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
12.
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
13.
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
14.
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
15.
Gregory, Louise, Rachel Besser, I. Karen Temple, Justin E. Davies, & Mehul Dattani. (2015). Mutations inBRAFare associated with septo-optic dysplasia and cardiofaciocutaneous syndrome. Endocrine Abstracts.
16.
Gregory, Louise, et al.. (2013). The management of moderate to high exudate in chronic wounds. British Journal of Nursing. 22(Sup3). P19–P19. 1 indexed citations
17.
Bancalari, Rodrigo, Louise Gregory, Mark J. McCabe, & Mehul Dattani. (2012). Developmental Biology of GH Secretion, Growth and Treatment. Endocrine development.
18.
Bancalari, Rodrigo, Louise Gregory, Mark J. McCabe, & Mehul Dattani. (2012). Pituitary Gland Development: An Update. Endocrine development. 23. 1–15. 41 indexed citations
19.
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.
20.
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

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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