Delphine Mallet

1.7k total citations
37 papers, 966 citations indexed

About

Delphine Mallet is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Delphine Mallet has authored 37 papers receiving a total of 966 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 14 papers in Genetics and 10 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Delphine Mallet's work include Sexual Differentiation and Disorders (20 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers) and Hormonal and reproductive studies (8 papers). Delphine Mallet is often cited by papers focused on Sexual Differentiation and Disorders (20 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers) and Hormonal and reproductive studies (8 papers). Delphine Mallet collaborates with scholars based in France, New Caledonia and Switzerland. Delphine Mallet's co-authors include Dominique Pelletier, Yves Morel, Florence Roucher‐Boulez, Ingrid Plotton, M David, Patricia Bretones, Frédérique Dijoud, Laurence Michel‐Calemard, Véronique Tardy and Laurent Wantiez and has published in prestigious journals such as Journal of Clinical Investigation, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Delphine Mallet

36 papers receiving 943 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Delphine Mallet France 16 380 302 241 223 203 37 966
Frederic A. Reid United States 11 157 0.4× 173 0.6× 161 0.7× 59 0.3× 62 0.3× 24 999
Roberto Pérez‐Castañeda Mexico 19 168 0.4× 318 1.1× 38 0.2× 103 0.5× 296 1.5× 61 1.0k
P.J. O'Shaughnessy United Kingdom 16 338 0.9× 66 0.2× 332 1.4× 44 0.2× 163 0.8× 28 1.1k
Akira Shinoda Japan 24 248 0.7× 160 0.5× 260 1.1× 755 3.4× 499 2.5× 77 1.9k
Yuichi Sasayama Japan 18 289 0.8× 308 1.0× 88 0.4× 118 0.5× 108 0.5× 105 1.0k
José M. Guzmán Spain 18 46 0.1× 463 1.5× 240 1.0× 152 0.7× 71 0.3× 54 1.1k
Minyao Wu China 18 325 0.9× 97 0.3× 140 0.6× 98 0.4× 154 0.8× 31 992
Toshio Sekiguchi Japan 23 610 1.6× 71 0.2× 287 1.2× 18 0.1× 128 0.6× 86 1.5k
Xiangyun Li China 17 297 0.8× 108 0.4× 58 0.2× 130 0.6× 99 0.5× 73 750
Jianlin Wang China 15 218 0.6× 95 0.3× 61 0.3× 18 0.1× 94 0.5× 56 778

Countries citing papers authored by Delphine Mallet

Since Specialization
Citations

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

Fields of papers citing papers by Delphine Mallet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Delphine Mallet

This figure shows the co-authorship network connecting the top 25 collaborators of Delphine Mallet. A scholar is included among the top collaborators of Delphine Mallet 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 Delphine Mallet. Delphine Mallet 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.
Barat, Pascal, et al.. (2024). Neonatal salt wasting syndrome: Aldosterone synthase deficiency caused by a new splicing variant in CYP11B2. Archives de Pédiatrie. 31(2). 157–160. 1 indexed citations
2.
Lucas, Cécily, Kay‐Sara Sauter, Delphine Mallet, et al.. (2022). Loss of LGR4/GPR48 causes severe neonatal salt wasting due to disrupted WNT signaling altering adrenal zonation. Journal of Clinical Investigation. 133(4). 8 indexed citations
3.
Mallet, Delphine, Florence Roucher‐Boulez, Marie Bournez, et al.. (2022). Epileptic encephalopathy as a new feature of the sudden infant death with dysgenesis of the testes syndrome caused by TSPYL1 variants. American Journal of Medical Genetics Part A. 188(12). 3540–3545. 2 indexed citations
4.
Bouty, Aurore, Florence Roucher‐Boulez, Delphine Mallet, et al.. (2022). Steroid Profiling in the Amniotic Fluid: Reference Range for 12 Steroids and Interest in 21-Hydroxylase Deficiency. The Journal of Clinical Endocrinology & Metabolism. 108(5). e129–e138. 5 indexed citations
5.
Donaldson, Malcolm, et al.. (2022). Genotype, Mortality, Morbidity, and Outcomes of 3β-Hydroxysteroid Dehydrogenase Deficiency in Algeria. Frontiers in Endocrinology. 13. 867073–867073. 5 indexed citations
6.
Goiran, Claire, et al.. (2022). Sea snake diversity at the Entrecasteaux atolls, Coral Sea, as revealed by video observations at unbaited stations. Coral Reefs. 41(6). 1551–1556. 1 indexed citations
7.
Manouvrier‐Hanu, Sylvie, Maryse Cartigny, Françoise Paris, et al.. (2019). In cases of familial primary ovarian insufficiency and disorders of gonadal development, consider NR5A1/SF-1 sequence variants. Reproductive BioMedicine Online. 40(1). 151–159. 7 indexed citations
8.
Roucher‐Boulez, Florence, Delphine Mallet, Nicolas Chatron, et al.. (2019). Reversion SAMD9 Mutations Modifying Phenotypic Expression of MIRAGE Syndrome and Allowing Inheritance in a Usually de novo Disorder. Frontiers in Endocrinology. 10. 625–625. 16 indexed citations
9.
Mallet, Delphine, Alexandre Janin, Rita Menassa, et al.. (2018). Aberrant Splicing Is the Pathogenicity Mechanism of the p.Glu314Lys Variant in CYP11A1 Gene. Frontiers in Endocrinology. 9. 491–491. 15 indexed citations
10.
Morel, Yves, et al.. (2016). Evolution of steroids during pregnancy: Maternal, placental and fetal synthesis. Annales d Endocrinologie. 77(2). 82–89. 83 indexed citations
11.
Parween, Shaheena, Florence Roucher‐Boulez, Christa E. Flück, et al.. (2016). P450 Oxidoreductase Deficiency: Loss of Activity Caused by Protein Instability From a Novel L374H Mutation. The Journal of Clinical Endocrinology & Metabolism. 101(12). 4789–4798. 18 indexed citations
12.
Morel, Yves, et al.. (2015). A late 17α-hydroxylase deficiency diagnosis that leads to the discovery of a new CYP17 gene mutation. Annales d Endocrinologie. 76(1). 71–74. 4 indexed citations
13.
14.
Pelletier, Dominique, et al.. (2012). Remote High-Definition Rotating Video Enables Fast Spatial Survey of Marine Underwater Macrofauna and Habitats. PLoS ONE. 7(2). e30536–e30536. 39 indexed citations
15.
Lekarev, Oksana, Delphine Mallet, Tony Yuen, Yves Morel, & Maria I. New. (2011). Congenital lipoid adrenal hyperplasia (a rare form of adrenal insufficiency and ambiguous genitalia) caused by a novel mutation of the steroidogenic acute regulatory protein gene. European Journal of Pediatrics. 171(5). 787–793. 8 indexed citations
16.
Morel, Yves, Ingrid Plotton, Delphine Mallet, et al.. (2011). Studies of a Cohort of 46,XY with DSD Including Steroid Biosynthesis Deficiencies. Advances in experimental medicine and biology. 707. 15–17. 7 indexed citations
17.
Coutant, R., Delphine Mallet, Najiba Lahlou, et al.. (2007). Heterozygous Mutation of Steroidogenic Factor-1 in 46,XY Subjects May Mimic Partial Androgen Insensitivity Syndrome. The Journal of Clinical Endocrinology & Metabolism. 92(8). 2868–2873. 63 indexed citations
18.
Flück, Christa E., Alexander Maret, Delphine Mallet, et al.. (2005). A Novel Mutation L260P of the Steroidogenic Acute Regulatory Protein Gene in Three Unrelated Patients of Swiss Ancestry with Congenital Lipoid Adrenal Hyperplasia. The Journal of Clinical Endocrinology & Metabolism. 90(9). 5304–5308. 40 indexed citations
19.
Feyaerts, Axel, Maguelone G. Forest, Yves Morel, et al.. (2002). Endocrine Screening in 32 Consecutive Patients with Hypospadias. The Journal of Urology. 168(2). 720–725. 32 indexed citations
20.
Guieu, Régis, Christiane Devaux, G. Bechis, et al.. (1998). Adenosine and Migraine. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 25(1). 55–58. 37 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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