Muriel Houang

2.9k total citations
40 papers, 1.4k citations indexed

About

Muriel Houang is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Muriel Houang has authored 40 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 13 papers in Genetics and 12 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Muriel Houang's work include Sexual Differentiation and Disorders (11 papers), Genetic Syndromes and Imprinting (8 papers) and Hormonal and reproductive studies (5 papers). Muriel Houang is often cited by papers focused on Sexual Differentiation and Disorders (11 papers), Genetic Syndromes and Imprinting (8 papers) and Hormonal and reproductive studies (5 papers). Muriel Houang collaborates with scholars based in France, United Kingdom and United States. Muriel Houang's co-authors include Yves Le Bouc, Irène Netchine, Sylvie Cabrol, Christine Gicquel, Véronique Barbu, Nathalie Thibaud, Fabienne Danton, Anne‐Marie Bertrand, Sylvie Rossignol and Lydie Bürglen and has published in prestigious journals such as The Lancet, Nature Genetics and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Muriel Houang

37 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Muriel Houang France	18	654	587	503	368	152	40	1.4k
Catherine Pienkowski France	25	839 1.3×	671 1.1×	282 0.6×	504 1.4×	112 0.7×	88	2.2k
B Boscherini Italy	23	659 1.0×	460 0.8×	193 0.4×	779 2.1×	188 1.2×	87	1.6k
Marita Lipsanen‐Nyman Finland	23	755 1.2×	575 1.0×	337 0.7×	153 0.4×	70 0.5×	46	1.4k
Nagayasu Toyoda Japan	23	263 0.4×	149 0.3×	224 0.4×	122 0.3×	92 0.6×	90	1.5k
C. Adamsbaum France	17	223 0.3×	177 0.3×	75 0.1×	136 0.4×	66 0.4×	57	712
Manuela Caruso‐Nicoletti Italy	12	259 0.4×	257 0.4×	105 0.2×	432 1.2×	39 0.3×	41	876
Hidetoshi Fujita Japan	22	423 0.6×	69 0.1×	309 0.6×	37 0.1×	383 2.5×	55	1.5k
D. Healy Australia	27	501 0.8×	221 0.4×	650 1.3×	254 0.7×	81 0.5×	59	2.8k
Darren Fowler United Kingdom	18	300 0.5×	140 0.2×	279 0.6×	48 0.1×	169 1.1×	40	1.3k
Daiichiro Hasegawa Japan	18	366 0.6×	153 0.3×	129 0.3×	39 0.1×	70 0.5×	105	1.2k

Countries citing papers authored by Muriel Houang

Since Specialization

Citations

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

Fields of papers citing papers by Muriel Houang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Muriel Houang

This figure shows the co-authorship network connecting the top 25 collaborators of Muriel Houang. A scholar is included among the top collaborators of Muriel Houang 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 Muriel Houang. Muriel Houang 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

Nguyen‐Khoa, Thao, Caroline Moreau, Jean Fiet, et al.. (2025). Advances in congenital adrenal hyperplasia newborn screening: 11-ketotestosterone and 21-deoxycortisone as additional discriminatory biomarkers. European Journal of Endocrinology. 193(6). 677–686.

Eguether, Thibaut, Jean Fiet, Yves Le Bouc, et al.. (2022). A proof of concept of a machine learning algorithm to predict late-onset 21-hydroxylase deficiency in children with premature pubic hair. The Journal of Steroid Biochemistry and Molecular Biology. 220. 106085–106085. 5 indexed citations

Messiaen, Claude, Muriel Houang, Bruno Donadille, et al.. (2021). Age at diagnosis in patients with chronic congenital endocrine conditions: a regional cohort study from a reference center for rare diseases. Orphanet Journal of Rare Diseases. 16(1). 469–469. 3 indexed citations

Peycelon, Matthieu, Lamisse Mansour‐Hendili, Capucine Hyon, et al.. (2017). Recurrent Intragenic Duplication within the <b><i>NR5A1</i></b> Gene and Severe Proximal Hypospadias. Sexual Development. 11(5-6). 293–297. 6 indexed citations

Schnabel, Dirk, et al.. (2016). Acceptance of a reusable self-injection device for recombinant human growth hormone: final data from a questionnaire-based, cross-sectional, international, multicenter, observational study in pediatric patients. Medical Devices Evidence and Research. Volume 9. 317–324. 3 indexed citations

Dufourg, Marie‐Noëlle, Laurence Périn, Muriel Houang, et al.. (2015). Silver Russell syndrome: A Cause of Partial IGF1 Resistance?. 84. 1 indexed citations

Simon, Dominique, Emmanuel Écosse, Anne Paulsen, et al.. (2015). Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty. European Journal of Endocrinology. 174(1). 1–8. 76 indexed citations

Simon, Dominique, Anne Paulsen, Delphine Zénaty, et al.. (2014). Mutations in the Maternally Imprinted Gene MKRN3 are a Frequent Cause of Familial Central Precocious Puberty. 1 indexed citations

Philibert, Pascal, Françoise Paris, Françoise Audran, et al.. (2011). Phenotypic Variation of SF1 Gene Mutations. Advances in experimental medicine and biology. 707. 67–72. 11 indexed citations

10.

Houang, Muriel, Yves Le Bouc, Jean‐Claude Carel, et al.. (2011). DNA polymorphisms of the KiSS1 3′ Untranslated region interfere with the folding of a G-rich sequence into G-quadruplex. Molecular and Cellular Endocrinology. 351(2). 239–248. 24 indexed citations

11.

Netchine, Irène, Salah Azzi, Muriel Houang, et al.. (2009). Partial Primary Deficiency of Insulin-Like Growth Factor (IGF)-I Activity Associated withIGF1Mutation Demonstrates Its Critical Role in Growth and Brain Development. The Journal of Clinical Endocrinology & Metabolism. 94(10). 3913–3921. 107 indexed citations

12.

Portnoï, Marie‐France, Nicolas Gruchy, Sandrine Marlin, et al.. (2007). Midline defects in deletion 18p syndrome: clinical and molecular characterization of three patients. Clinical Dysmorphology. 16(4). 247–252. 34 indexed citations

13.

Verkauskienė, Rasa, Catherine Dollfus, Martine Lévine, et al.. (2006). Serum Adiponectin and Leptin Concentrations in HIV-Infected Children with Fat Redistribution Syndrome. Pediatric Research. 60(2). 225–230. 23 indexed citations

14.

Dollfus, Catherine, Martine Lévine, Albert Faye, et al.. (2005). Longitudinal Evaluation and Risk Factors of Lipodystrophy and Associated Metabolic Changes in HIV-Infected Children. JAIDS Journal of Acquired Immune Deficiency Syndromes. 40(2). 161–168. 100 indexed citations

15.

Gicquel, Christine, Sylvie Rossignol, Sylvie Cabrol, et al.. (2005). Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome. Nature Genetics. 37(9). 1003–1007. 379 indexed citations

16.

Houang, Muriel, M Gourmelen, L Moatti, et al.. (2002). Hypogonadotrophic Hypogonadism Associated with Prelingual Deafness due to a Connexin 26 Gene Mutation. Journal of Pediatric Endocrinology and Metabolism. 15(2). 219–23. 14 indexed citations

17.

Ducos, Bertrand, Sylvie Cabrol, Muriel Houang, et al.. (2001). IGF Type 1 Receptor Ligand Binding Characteristics Are Altered in a Subgroup of Children with Intrauterine Growth Retardation. The Journal of Clinical Endocrinology & Metabolism. 86(11). 5516–5524. 16 indexed citations

18.

Houang, Muriel, Sylvie Cabrol, Laurence Périn, et al.. (2000). Insulin-like growth factor-I (IGF-I), insulin-like growth factor binding proteins (IGFBP) and insulin-like growth factor type I receptor in children with various status of chronic renal failure. Growth Hormone & IGF Research. 10(6). 332–341. 17 indexed citations

19.

Rodriguez‐Wallberg, Kenny A., E Thibaud, Muriel Houang, et al.. (1999). Follow up of precocious pseudopuberty associated with isolated ovarian follicular cysts. Archives of Disease in Childhood. 81(1). 53–56. 30 indexed citations

20.

Harper, Peter, R L Souhami, Muriel Houang, et al.. (1981). Computerized axial tomography in the pretreatment assessment of small-cell carcinoma of the bronchus. Cancer. 47(7). 1775–1780. 30 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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