John C. Achermann

11.7k total citations
130 papers, 6.1k citations indexed

About

John C. Achermann is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, John C. Achermann has authored 130 papers receiving a total of 6.1k indexed citations (citations by other indexed papers that have themselves been cited), including 98 papers in Molecular Biology, 78 papers in Genetics and 43 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in John C. Achermann's work include Sexual Differentiation and Disorders (76 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (67 papers) and Hormonal Regulation and Hypertension (21 papers). John C. Achermann is often cited by papers focused on Sexual Differentiation and Disorders (76 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (67 papers) and Hormonal Regulation and Hypertension (21 papers). John C. Achermann collaborates with scholars based in United Kingdom, United States and France. John C. Achermann's co-authors include J. Larry Jameson, Lin Lin, Gökhan Özışık, Bruno Ferraz‐de‐Souza, Masafumi Ito, Mehul Dattani, Joshua J. Meeks, Lucy Lin, Federica Buonocore and Lin Lin and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

John C. Achermann

126 papers receiving 6.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
John C. Achermann United Kingdom 47 4.4k 3.7k 1.8k 1.7k 715 130 6.1k
Tomonobu Hasegawa Japan 41 3.2k 0.7× 2.1k 0.6× 2.0k 1.1× 868 0.5× 386 0.5× 360 6.1k
Maki Fukami Japan 35 3.7k 0.8× 3.6k 1.0× 876 0.5× 787 0.5× 462 0.6× 307 5.9k
Ana Cláudia Latronico Brazil 50 3.5k 0.8× 2.7k 0.7× 2.2k 1.3× 3.9k 2.3× 132 0.2× 225 8.0k
Elaine Maria Frade Costa Brazil 32 2.1k 0.5× 1.4k 0.4× 940 0.5× 879 0.5× 576 0.8× 112 3.0k
Taneli Raivio Finland 38 2.5k 0.6× 1.8k 0.5× 1.1k 0.6× 2.4k 1.4× 68 0.1× 135 5.0k
Jörg Gromoll Germany 50 3.8k 0.9× 3.1k 0.8× 1.5k 0.8× 4.7k 2.8× 132 0.2× 156 7.9k
Jean‐Louis Chaussain France 41 2.1k 0.5× 1.6k 0.4× 2.1k 1.2× 882 0.5× 222 0.3× 106 4.3k
M. Zachmann Switzerland 41 2.7k 0.6× 1.3k 0.4× 2.6k 1.5× 863 0.5× 285 0.4× 181 4.8k
Martin Ritzén Sweden 32 2.1k 0.5× 838 0.2× 1.4k 0.8× 435 0.3× 334 0.5× 94 3.9k
Karel De Gendt Belgium 29 1.3k 0.3× 1.3k 0.3× 916 0.5× 1.7k 1.0× 91 0.1× 44 3.4k

Countries citing papers authored by John C. Achermann

Since Specialization
Citations

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

Fields of papers citing papers by John C. Achermann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John C. Achermann. 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 John C. Achermann. The network helps show where John C. Achermann may publish in the future.

Co-authorship network of co-authors of John C. Achermann

This figure shows the co-authorship network connecting the top 25 collaborators of John C. Achermann. A scholar is included among the top collaborators of John C. Achermann 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 John C. Achermann. John C. Achermann 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.
Houzelstein, Denis, Caroline Eozénou, Carlos F. Lagos, et al.. (2024). A conserved NR5A1-responsive enhancer regulates SRY in testis-determination. Nature Communications. 15(1). 2796–2796. 1 indexed citations
2.
Valle, Ignacio del, Matthew D. Young, Olumide Ogunbiyi, et al.. (2023). An integrated single-cell analysis of human adrenal cortex development. JCI Insight. 8(14). 10 indexed citations
3.
Bashamboo, Anu, Caroline Eozénou, Anne Jørgensen, et al.. (2018). Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children. The American Journal of Human Genetics. 102(3). 487–493. 65 indexed citations
4.
Farrugia, Marie‐Klaire, et al.. (2012). Clinical and gonadal features and early surgical management of 45,X/46,XY and 45,X/47,XYY chromosomal mosaicism presenting with genital anomalies. Journal of Pediatric Urology. 9(2). 139–144. 39 indexed citations
5.
Lin, Lin, John C. Achermann, Mark Harris, et al.. (2012). A novel NR5A1 variant in an infant with elevated testosterone from an Australasian cohort of 46,XY patients with disorders of sex development. Clinical Endocrinology. 78(4). 545–550. 20 indexed citations
6.
Frapsauce, Cynthia, Célia Ravel, Marie Legendre, et al.. (2011). Birth after TESE-ICSI in a man with hypogonadotropic hypogonadism and congenital adrenal hypoplasia linked to a DAX-1 (NR0B1) mutation. Human Reproduction. 26(3). 724–728. 32 indexed citations
7.
Achermann, John C., Erica A. Eugster, & Dorothy I. Shulman. (2011). Ambiguous Genitalia. The Journal of Clinical Endocrinology & Metabolism. 96(3). 33A–33A. 2 indexed citations
8.
Padidela, Raja, et al.. (2011). The growth hormone receptor gene deleted for exon three (GHRd3) polymorphism is associated with birth and placental weight. Clinical Endocrinology. 76(2). 236–240. 13 indexed citations
9.
Ahmed, S. Faisal, John C. Achermann, Wiebke Arlt, et al.. (2011). UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development. Clinical Endocrinology. 75(1). 12–26. 99 indexed citations
10.
Bashamboo, Anu, Bruno Ferraz‐de‐Souza, Diana Lourenço, et al.. (2010). Human Male Infertility Associated with Mutations in NR5A1Encoding Steroidogenic Factor 1. The American Journal of Human Genetics. 87(5). 736–736. 3 indexed citations
11.
Metherell, Louise, Danielle Naville, G Halaby, et al.. (2009). Nonclassic Lipoid Congenital Adrenal Hyperplasia Masquerading as Familial Glucocorticoid Deficiency. The Journal of Clinical Endocrinology & Metabolism. 94(10). 3865–3871. 112 indexed citations
12.
Ferraz‐de‐Souza, Bruno, et al.. (2009). Novel targets of steroidogenic factor-1 (SF-1, NR5A1, Ad4BP) in the adrenal. UCL Discovery (University College London). 1 indexed citations
13.
Lin, Lin, Pascal Philibert, Bruno Ferraz‐de‐Souza, et al.. (2007). Heterozygous Missense Mutations in Steroidogenic Factor 1 (SF1/Ad4BP, NR5A1) Are Associated with 46,XY Disorders of Sex Development with Normal Adrenal Function. The Journal of Clinical Endocrinology & Metabolism. 92(3). 991–999. 150 indexed citations
14.
Vilain, Éric, John C. Achermann, Erica A. Eugster, et al.. (2007). We used to call them hermaphrodites. Genetics in Medicine. 9(2). 65–66. 23 indexed citations
15.
Köhler, Birgit, Lin Lin, Bruno Ferraz‐de‐Souza, et al.. (2007). Five novel mutations in steroidogenic factor 1 (SF1,NR5A1) in 46,XY patients with severe underandrogenization but without adrenal insufficiency. Human Mutation. 29(1). 59–64. 106 indexed citations
16.
Semple, Robert K., John C. Achermann, I. Sadaf Farooqi, et al.. (2005). Two Novel Missense Mutations in G Protein-Coupled Receptor 54 in a Patient with Hypogonadotropic Hypogonadism. The Journal of Clinical Endocrinology & Metabolism. 90(3). 1849–1855. 216 indexed citations
17.
Lin, Lin & John C. Achermann. (2004). Inherited adrenal hypoplasia: not just for kids!. Clinical Endocrinology. 60(5). 529–537. 18 indexed citations
18.
Mantovani, Giovanna, Gökhan Özışık, John C. Achermann, et al.. (2002). Hypogonadotropic Hypogonadism as a Presenting Feature of Late-Onset X-Linked Adrenal Hypoplasia Congenita. The Journal of Clinical Endocrinology & Metabolism. 87(1). 44–48. 76 indexed citations
19.
Achermann, John C., et al.. (2002). Clinical perspective: Genetic mutations in human reproductive disease. UCL Discovery (University College London). 1 indexed citations
20.
Achermann, John C., Masafumi Ito, Bernard L. Silverman, et al.. (2001). Missense Mutations Cluster within the Carboxyl-Terminal Region of DAX-1 and Impair Transcriptional Repression1. The Journal of Clinical Endocrinology & Metabolism. 86(7). 3171–3175. 62 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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