Ian T. Rose

613 total citations
7 papers, 286 citations indexed

About

Ian T. Rose is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, Ian T. Rose has authored 7 papers receiving a total of 286 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Endocrinology, Diabetes and Metabolism, 6 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Ian T. Rose's work include Sexual Differentiation and Disorders (6 papers), Hormonal and reproductive studies (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Ian T. Rose is often cited by papers focused on Sexual Differentiation and Disorders (6 papers), Hormonal and reproductive studies (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Ian T. Rose collaborates with scholars based in United Kingdom, Germany and Netherlands. Ian T. Rose's co-authors include Nils Krone, Wiebke Arlt, Silvia Parajes, Vivek Dhir, Angela E. Taylor, Nicole Reisch, Wolfgang Högler, Christiaan F. Mooij, Roland H. Stimson and Brian R. Walker and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Endocrinology and Clinical Endocrinology.

In The Last Decade

Ian T. Rose

6 papers receiving 282 citations

Peers

Countries citing papers authored by Ian T. Rose

Since Specialization

Citations

This map shows the geographic impact of Ian T. Rose'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 Ian T. Rose with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ian T. Rose more than expected).

Fields of papers citing papers by Ian T. Rose

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ian T. Rose. 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 Ian T. Rose. The network helps show where Ian T. Rose may publish in the future.

Co-authorship network of co-authors of Ian T. Rose

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Characterization of the molecular genetic pathology in patients with 11β‐hydroxylase deficiency 2015 ·Clinical Endocrinology ·Christiaan F. Mooij, Silvia Parajes, Ian T. Rose, Angela E. Taylor, Taner Bayraktaroğlu, John Wass, John Connell, David Ray, Wiebke Arlt, Nils Krone	17
2	A Diagnosis Not to Be Missed: Nonclassic Steroid 11β-Hydroxylase Deficiency Presenting With Premature Adrenarche and Hirsutism 2013 ·The Journal of Clinical Endocrinology & Metabolism ·Nicole Reisch, Wolfgang Högler, Silvia Parajes, Ian T. Rose, Vivek Dhir, (unknown), Wiebke Arlt, Nils Krone	44
3	Redefining the Initiation and Maintenance of Zebrafish Interrenal Steroidogenesis by Characterizing the Key Enzyme Cyp11a2 2013 ·Endocrinology ·Silvia Parajes, Aliesha Griffin, Angela E. Taylor, Ian T. Rose, Irene Miguel-Escalada, Yavor Hadzhiev, Wiebke Arlt, Cedric Shackleton, Ferenc Müller, Nils Krone	37
4	Genotype-Phenotype Correlation in 153 Adult Patients With Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Analysis of the United Kingdom Congenital Adrenal Hyperplasia Adult Study Executive (CaHASE) Cohort 2013 ·The Journal of Clinical Endocrinology & Metabolism ·Nils Krone, Ian T. Rose, Debbie Willis, James Hodson, Sarah H. Wild, (unknown), Stefanie Hahner, Silvia Parajes, Roland H. Stimson, Thang S. Han, Paul Carroll, Gerry Conway, Brian R. Walker, Fiona MacDonald, Richard Ross, Wiebke Arlt, (unknown)	76
5	A Novel Entity of Clinically Isolated Adrenal Insufficiency Caused by a Partially Inactivating Mutation of the Gene Encoding for P450 Side Chain Cleavage Enzyme (CYP11A1) 2011 ·The Journal of Clinical Endocrinology & Metabolism ·Silvia Parajes, Clemens Kamrath, Ian T. Rose, Angela E. Taylor, Christiaan F. Mooij, Vivek Dhir, Joachim Grötzinger, Wiebke Arlt, Nils Krone	39
6	Functional Consequences of Seven Novel Mutations in theCYP11B1Gene: Four Mutations Associated with Nonclassic and Three Mutations Causing Classic 11β-Hydroxylase Deficiency 2010 ·The Journal of Clinical Endocrinology & Metabolism ·Silvia Parajes, Lourdes Loidi, Nicole Reisch, Vivek Dhir, Ian T. Rose, (unknown), Marcus Quinkler, Gerard S. Conway, Lidia Castro-Feijóo, David Araújo‐Vilar, Manuel Pombo, Fernando Domı́nguez, Emma L. Williams, Trevor Cole, Jeremy Kirk, (unknown), Gill Rumsby, Wiebke Arlt, Nils Krone	72
7	Current management, morbidity and genotypephenotype correlation in adults with congenital adrenal hyperplasia – analysis of the United Kingdom congenital adrenal hyperplasia adult study executive (CaHASE) cohort [Abstract] 2009 ·ORCA Online Research @Cardiff ·Nils Krone, Debbie Willis, Ian T. Rose, Andrew H. Crosby, Sarah H. Wild, (unknown), Stefanie Hahner, Thang S. Han, Roland H. Stimson, Paul Carroll, (unknown), Aled Rees, Brian R. Walker, Fiona MacDonald, Richard Ross, Wiebke Arlt	1

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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