Françoise Audran

1.6k total citations
29 papers, 802 citations indexed

About

Françoise Audran is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Urology. According to data from OpenAlex, Françoise Audran has authored 29 papers receiving a total of 802 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 11 papers in Endocrinology, Diabetes and Metabolism and 10 papers in Urology. Recurrent topics in Françoise Audran's work include Sexual Differentiation and Disorders (21 papers), Hormonal and reproductive studies (10 papers) and Urological Disorders and Treatments (10 papers). Françoise Audran is often cited by papers focused on Sexual Differentiation and Disorders (21 papers), Hormonal and reproductive studies (10 papers) and Urological Disorders and Treatments (10 papers). Françoise Audran collaborates with scholars based in France, United States and Tunisia. Françoise Audran's co-authors include Charles Sultan, Pascal Philibert, Françoise Paris, Serge Lumbroso, Nicolas Kalfa, Delphine Zénaty, C. Sultan, Michel Polak, Lin Lin and S. Soskin and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Gene.

In The Last Decade

Françoise Audran

28 papers receiving 772 citations

Peers

Countries citing papers authored by Françoise Audran

Since Specialization

Citations

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

Fields of papers citing papers by Françoise Audran

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Françoise Audran

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Familial Mutation of NR5A1/SF-1 Gene Associated with DSD and Spleen Agenesis: A New Syndrome? 2015 ·Pascal Philibert, Françis Poulat, Françoise Audran, Maryse Cartigny, Françoise Paris, Charles Sultan, Sylvie Manouvrier‐Hanu	1
2	Mutational screening of SF1 and WNT4 in Tunisian women with premature ovarian failure 2012 ·Gene ·(unknown), (unknown), Nouha Bouali, (unknown), Françoise Audran, R. Braham, Hatem Elghezal, Charles Sultan, Saad Hasan Mohammed Ali	15
3	Polymorphisms of MAMLD1 gene in hypospadias 2011 ·Journal of Pediatric Urology ·Nicolas Kalfa, Fernando Cassorla, Françoise Audran, (unknown), Pascal Philibert, Christophe Béroud, Jean-Michel Guys, Rachel Reynaud, P Alessandrini, Karl‐Heinz Wagner, Jean Bréaud, Jean Stéphane Valla, (unknown), J.P. Daurès, Laurence S. Baskin, Maki Fukami, Tsutomu Ogata, Charles Sultan	26
4	Phenotypic Variation of SF1 Gene Mutations 2011 ·Advances in experimental medicine and biology ·Pascal Philibert, Françoise Paris, Françoise Audran, Nicolas Kalfa, Michel Polak, E Thibaud, Graziella Pinto, Muriel Houang, Delphine Zénaty, Juliane Léger, (unknown), Catherine Pienkowski, Silvia Einaudi, Durval Damiani, Svetlana Ten, (unknown), Françis Poulat, Charles Sultan	11
5	‘Idiopathic’ partial androgen insensitivity syndrome in 28 newborn and infant males: impact of prenatal exposure to environmental endocrine disruptor chemicals? 2011 ·European Journal of Endocrinology ·Laura Gaspari, Françoise Paris, Pascal Philibert, Françoise Audran, Mattéa Orsini, Nadège Servant, Laurent Maı̈moun, Nicolas Kalfa, Charles Sultan	20
6	Isolated ‘idiopathic’ micropenis: hidden genetic defects? 2011 ·International Journal of Andrology ·Françoise Paris, (unknown), Amrit Bhangoo, Svetlana Ten, N. Lahlou, Françoise Audran, Nadège Servant, Françis Poulat, Pascal Philibert, Charles Sultan	19
7	Isolated micropenis reveals partial androgen insensitivity syndrome confirmed by molecular analysis 2010 ·Asian Journal of Andrology ·Amrit Bhangoo, Françoise Paris, Pascal Philibert, Françoise Audran, Svetlana Ten, Charles Sultan	24
8	Undervirilization in XY newborns may hide a 5α‐reductase deficiency: report of three new SRD5A2 gene mutations 2010 ·International Journal of Andrology ·Laurent Maı̈moun, Pascal Philibert, (unknown), Françoise Audran, Catherine Pienkowski, F Kurtz, (unknown), Maryse Cartigny, Charles Sultan	23
9	Steroidogenic factor-1 (SF-1) gene mutation as a frequent cause of primary amenorrhea in 46,XY female adolescents with low testosterone concentration 2010 ·Reproductive Biology and Endocrinology ·Pascal Philibert, (unknown), Delphine Zénaty, E Thibaud, Michel Polak, (unknown), James Lespinasse, I. Raingeard, Nadège Servant, Françoise Audran, Françoise Paris, Charles Sultan	61
10	Phenotype, hormonal profile and genotype of subjects with partial androgen insensitivity syndrome: report of a family with four adult males and one child with disorder of sexual differentiation 2009 ·Andrologia ·Bindu Kulshreshtha, Pascal Philibert, (unknown), Françoise Audran, Françoise Paris, Madan Lal Khurana, Ariachery C. Ammini, (unknown)	9
11	Mother-to-Son Transmission of a Luteinizing Hormone Receptor Activating Mutation in a Prepubertal Child with Testotoxicosis 2009 ·Journal of Pediatric Endocrinology and Metabolism ·Eunice Marumudi, Pascal Philibert, Bindu Kulshreshtha, Françoise Audran, Françoise Paris, Charles Sultan, Ariachery C. Ammini	2
12	Complete androgen insensitivity syndrome is frequently due to premature stop codons in exon 1 of the androgen receptor gene: an international collaborative report of 13 new mutations 2009 ·Fertility and Sterility ·Pascal Philibert, Françoise Audran, Catherine Pienkowski, Isabelle Morange, Birgit Köhler, Elisabeth Flori, (unknown), Catherine Dacou‐Voutetakis, (unknown), A.M. Guedj, Hubert Journel, (unknown), (unknown), Svetlana Ten, Philippe Bouchard, Françoise Paris, Charles Sultan	27
13	Mutations of CXorf6 are associated with a range of severities of hypospadias 2008 ·European Journal of Endocrinology ·Nicolas Kalfa, Benchun Liu, Ophir D. Klein, Françoise Audran, (unknown), Mei Cao, Charles Sultan, Laurence S. Baskin	47
14	Mutational analysis of steroidogenic factor 1 (NR5a1) in 24 boys with bilateral anorchia: a French collaborative study 2007 ·Human Reproduction ·Pascal Philibert, Delphine Zénaty, Lin Lin, S. Soskin, Françoise Audran, Juliane Léger, John C. Achermann, C. Sultan	94
15	Activating Mutations of the Stimulatory G Protein in Juvenile Ovarian Granulosa Cell Tumors: A New Prognostic Factor? 2006 ·The Journal of Clinical Endocrinology & Metabolism ·Nicolas Kalfa, (unknown), Catherine Patte, Pierre Duvillard, Françoise Audran, Catherine Pienkowski, E Thibaud, Raja Brauner, C Lecointre, Dominique Plantaz, A.M. Guedj, Françoise Paris, Pierre Baldet, Serge Lumbroso, Charles Sultan	70
16	Association between androgen receptor gene polymorphism and bone density in older women using hormone replacement therapy 2006 ·Maturitas ·F. Rétornaz, Françoise Paris, Serge Lumbroso, Françoise Audran, (unknown), Cécile Michelon, Claude Jeandel, Charles Sultan, Hubert Blain	3
17	Searching for somatic mutations in McCune–Albright syndrome: a comparative study of the peptidic nucleic acid versus the nested PCR method based on 148 DNA samples 2006 ·European Journal of Endocrinology ·Nicolas Kalfa, Pascal Philibert, Françoise Audran, (unknown), Tamara S. Hannon, Serge Lumbroso, C. Sultan	20
18	A new mutation of the androgen receptor, P817A, causing partial androgen insensitivity syndrome: in vitro and structural analysis 2004 ·Journal of Molecular Endocrinology ·Serge Lumbroso, Alexandre Wagschal, William Bourguet, Virginie Georget, Inas Mazen, Nadège Servant, Françoise Audran, Charles Sultan, Gilles Auzou	9
19	Disorders of Androgen Action 2002 ·Seminars in Reproductive Medicine ·Charles Sultan, Serge Lumbroso, Françoise Paris, Claire Jeandel, Béatrice Térouanne, Charles Belon, Françoise Audran, Nicolas Poujol, Virginie Georget, (unknown), Stéphan Jalaguier, Gilles Auzou, Jean‐Claude Nicolas	36
20	Increased oestradiol level in seminal plasma in infertile men 1993 ·Human Reproduction ·Louis Bujan, Roger Mieusset, Françoise Audran, Serge Lumbroso, Charles Sultan	51

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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