Latifa Hilal

696 total citations
15 papers, 569 citations indexed

About

Latifa Hilal is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Latifa Hilal has authored 15 papers receiving a total of 569 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Endocrinology, Diabetes and Metabolism and 4 papers in Genetics. Recurrent topics in Latifa Hilal's work include Skin and Cellular Biology Research (3 papers), Neuroendocrine Tumor Research Advances (2 papers) and Connexins and lens biology (2 papers). Latifa Hilal is often cited by papers focused on Skin and Cellular Biology Research (3 papers), Neuroendocrine Tumor Research Advances (2 papers) and Connexins and lens biology (2 papers). Latifa Hilal collaborates with scholars based in France, Morocco and United Kingdom. Latifa Hilal's co-authors include Michel Goossens, Alain Hovnanian, Ariane Rochat, Yann Barrandon, Célia Fourrier, Cathérine Prost, Thomas Larrieu, Nathalie Sans, Lucile Capuron and Sophie Layé and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Journal of Investigative Dermatology.

In The Last Decade

Latifa Hilal

14 papers receiving 555 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Latifa Hilal France	11	240	220	155	87	68	15	569
John Morten United Kingdom	14	18 0.1×	454 2.1×	117 0.8×	29 0.3×	30 0.4×	36	666
Anne Suttkus Germany	12	191 0.8×	200 0.9×	46 0.3×	17 0.2×	7 0.1×	17	525
Nick Jacobsen United Kingdom	11	211 0.9×	463 2.1×	573 3.7×	50 0.6×	5 0.1×	11	840
Pierre-Marc Bouloux United Kingdom	15	74 0.3×	364 1.7×	242 1.6×	9 0.1×	2 0.0×	27	866
Erzsébet Gáspár Germany	13	221 0.9×	135 0.6×	33 0.2×	18 0.2×	4 0.1×	17	691
Yoshiro Kameyama Japan	14	38 0.2×	231 1.1×	76 0.5×	10 0.1×	9 0.1×	37	527
Hisashi Nakamura Japan	13	39 0.2×	235 1.1×	77 0.5×	87 1.0×	7 0.1×	32	680
T. Yamaai Japan	13	45 0.2×	246 1.1×	36 0.2×	26 0.3×	2 0.0×	23	612
Sanae A. Kanzawa United States	6	27 0.1×	217 1.0×	12 0.1×	30 0.3×	32 0.5×	7	472
May C. Ng United States	11	29 0.1×	188 0.9×	28 0.2×	14 0.2×	33 0.5×	20	547

Countries citing papers authored by Latifa Hilal

Since Specialization

Citations

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

Fields of papers citing papers by Latifa Hilal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Latifa Hilal

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

All Works

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15 of 15 papers shown

Hilal, Latifa, Laila Hessissen, M. El Khorassani, et al.. (2018). Cytogenetic Profile of Moroccan Pediatric Acute Lymphoblastic Leukemia: Analysis of 155 Cases With a Review of the Literature. Clinical Lymphoma Myeloma & Leukemia. 18(6). e241–e248. 6 indexed citations

Hilal, Latifa, et al.. (2015). Molecular analysis of the rearranged during transfection proto-oncogene in Moroccan patients with medullary thyroid carcinoma. Clinical Cancer Investigation Journal. 4(2). 188–188.

Sobrier, Marie‐Laure, Hinde Iraqi, Irène Netchine, et al.. (2014). Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism. Clinical Endocrinology. 82(6). 876–884. 11 indexed citations

Larrieu, Thomas, Latifa Hilal, Célia Fourrier, et al.. (2014). Nutritional omega-3 modulates neuronal morphology in the prefrontal cortex along with depression-related behaviour through corticosterone secretion. Translational Psychiatry. 4(9). e437–e437. 113 indexed citations

Berraho, A., et al.. (2013). Genotype-Phenotype Correlation in Moroccan Patients With Primary Congenital Glaucoma. Journal of Glaucoma. 24(4). 297–305. 17 indexed citations

Hilal, Latifa, et al.. (2010). Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: three novel mutations in CYP1B1.. PubMed. 16. 1215–26. 30 indexed citations

Hilal, Latifa, et al.. (2008). Unusual Phenotypic Features in a Patient with a Novel Splice Mutation in the GHRHR Gene. Molecular Medicine. 14(5-6). 286–292. 23 indexed citations

Benazzouz, Bouchra, et al.. (2008). [C634R mutation of the protooncongene RET and molecular diagnosis in multiple endocrine neoplasia type 2 in a large Moroccan family].. PubMed. 95(4). 457–63. 2 indexed citations

Benazzouz, Bouchra, et al.. (2006). Caractérisation de la mutation C634Y du proto-oncogène RET dans une famille marocaine de néoplasie endocrinienne multiple de type 2A. Annales d Endocrinologie. 67(1). 21–26. 1 indexed citations

10.

Nandrot, Emeline F., C. Slingsby, Bouchra Benazzouz, et al.. (2003). Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataracts. Journal of Medical Genetics. 40(4). 262–267. 79 indexed citations

11.

Hilal, Latifa, Emeline F. Nandrot, Bouchra Benazzouz, et al.. (2002). Evidence of clinical and genetic heterogeneity in autosomal dominant congenital cerulean cataracts. Ophthalmic Genetics. 23(4). 199–208. 11 indexed citations

12.

Hovnanian, Alain, Latifa Hilal, C Blanchet‐Bardon, et al.. (1995). DNA-Based Prenatal Diagnosis of Generalized Recessive Dystrophic Epidermolysis Bullosa in Six Pregnancies at Risk for Recurrence. Journal of Investigative Dermatology. 104(4). 456–461. 38 indexed citations

13.

Hilal, Latifa, Ariane Rochat, Philippe Duquesnoy, et al.. (1993). A homozygous insertion–deletion in the type VII collagen gene (COL7A1) in Hallopeau–Siemens dystrophic epidermolysis bullosa. Nature Genetics. 5(3). 287–293. 109 indexed citations

14.

Hovnanian, Alain, Latifa Hilal, Ariane Rochat, et al.. (1993). A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex. Nature Genetics. 3(4). 327–332. 114 indexed citations

15.

Hilal, Latifa, et al.. (1987). 20-Hydroxyecdysone regulates cytoplasmic actin gene expression inDrosophilacultured cells. Nucleic Acids Research. 15(6). 2549–2561. 15 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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