О. В. Фофанова

458 total citations
16 papers, 345 citations indexed

About

О. В. Фофанова is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, О. В. Фофанова has authored 16 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Endocrinology, Diabetes and Metabolism, 9 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in О. В. Фофанова's work include Growth Hormone and Insulin-like Growth Factors (12 papers), RNA modifications and cancer (4 papers) and Genetic Syndromes and Imprinting (3 papers). О. В. Фофанова is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (12 papers), RNA modifications and cancer (4 papers) and Genetic Syndromes and Imprinting (3 papers). О. В. Фофанова collaborates with scholars based in Russia, Japan and United Kingdom. О. В. Фофанова's co-authors include И. И. Дедов, Noboru Takamura, Shunichi Yamashita, Oleg V. Evgrafov, Ivo J.P. Arnhold, Joy D. Cogan, İffet Bircan, Berenice B. Mendonça, Wei Wu and John A. Phillips and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and American Journal of Roentgenology.

In The Last Decade

О. В. Фофанова

14 papers receiving 326 citations

Peers

Countries citing papers authored by О. В. Фофанова

Since Specialization

Citations

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

Fields of papers citing papers by О. В. Фофанова

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by О. В. Фофанова. 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 О. В. Фофанова. The network helps show where О. В. Фофанова may publish in the future.

Co-authorship network of co-authors of О. В. Фофанова

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Ефективність застосування Лаферобіону в дітей із рецидивуючим бронхообструктивним синдромом, які часто хворіють на гострі респіраторні захворювання 2014 ·SHILAP Revista de lepidopterología ·(unknown), О. В. Фофанова, (unknown), (unknown)	0
2	[Study of the effectiveness and safety of Rastan in children with growth hormone deficiency and Turner's syndrome]. 2007 ·PubMed ·И. И. Дедов, (unknown), О. В. Фофанова, (unknown), (unknown), Alexander V. Misharin, Valentina Peterkova	0
3	A novel splicing mutation in exon 4 (456G>A) of the GH1 gene in a patient with congenital isolated growth hormone deficiency 2006 ·HORMONES ·О. В. Фофанова, Oleg V. Evgrafov, A. V. Polyakov, Valentina Peterkova, И. И. Дедов	4
4	GH-1 gene splicing mutations: Molecular basis of hereditary isolated growth hormone deficiency in children 2006 ·Bulletin of Experimental Biology and Medicine ·О. В. Фофанова, Oleg V. Evgrafov, A. V. Polyakov, (unknown), И. И. Дедов	1
5	A Novel IVS2 −2A>T Splicing Mutation in theGH-1Gene in Familial Isolated Growth Hormone Deficiency Type II in the Spectrum of Other Splicing Mutations in the Russian Population 2003 ·The Journal of Clinical Endocrinology & Metabolism ·О. В. Фофанова, Oleg V. Evgrafov, A. V. Polyakov, А. Б. Полтараус, Valentina Peterkova, И. И. Дедов	29
6	Триада (гипоплазия аденогипофиза и гипофизарной ножки, эктопия нейрогипофиза) в МР-томографической диагностике 2001 ·И. И. Дедов, О. В. Фофанова, (unknown), (unknown), Valentina Peterkova	1
7	MR Imaging of the Pituitary Gland in Children and Young Adults with Congenital Combined Pituitary Hormone Deficiency Associated with PROP1 Mutations 2000 ·American Journal of Roentgenology ·О. В. Фофанова, Noboru Takamura, Eiichi Kinoshita, (unknown), (unknown), И. И. Дедов, Valentina Peterkova, Shunichi Yamashita	46
8	Gene analysis of PROP1 in dwarfism with combined pituitary hormone deficiency 1999 ·Growth Hormone & IGF Research ·Noboru Takamura, О. В. Фофанова, Eiichi Kinoshita, Shunichi Yamashita	7
9	A Mutational Hot Spot in the Prop-1 Gene in Russian Children with Combined Pituitary Hormone Deficiency 1998 ·Pituitary ·О. В. Фофанова, Noboru Takamura, (unknown), John S. Parks, Milton R. Brown, (unknown), Oleg V. Evgrafov, Н. П. Гончаров, (unknown), И. И. Дедов, Shunichi Yamashita	42
10	Rarity of PIT1 involvement in children from Russia with combined pituitary hormone deficiency 1998 ·American Journal of Medical Genetics ·О. В. Фофанова, Noboru Takamura, (unknown), (unknown), (unknown), (unknown), Oleg V. Evgrafov, И. И. Дедов, Н. П. Гончаров, Shunichi Yamashita	47
11	The PROP1 2-Base Pair Deletion Is a Common Cause of Combined Pituitary Hormone Deficiency1 1998 ·The Journal of Clinical Endocrinology & Metabolism ·Joy D. Cogan, Wei Wu, John A. Phillips, Ivo J.P. Arnhold, Ana Agapito, О. В. Фофанова, (unknown), İffet Bircan, (unknown), Berenice B. Mendonça	143
12	A Missense Mutation of C1659 in the Fibroblast Growth Factor Receptor 3 Gene in Russian Patients with Hypochondroplasia. 1998 ·Endocrine Journal ·О. В. Фофанова, Noboru Takamura, Eiichi Kinoshita, (unknown), (unknown), (unknown), Oleg V. Evgrafov, Valentina Peterkova, Shunichi Yamashita	4
13	Somatotropic insufficiency in children and antip1tu1tary antibodies as characteristics of humoral immunity in patients and their parents 1996 ·Problems of Endocrinology ·О. В. Фофанова, Valentina Peterkova, (unknown), (unknown), (unknown), (unknown), Н. П. Гончаров, (unknown), (unknown), (unknown)	1
14	Syndrome Hutchinson-Gilford (progeria) 1995 ·Problems of Endocrinology ·О. В. Фофанова	3
15	Use of the genetic engineering growth hormone SAISEN in children with somatotropic insufficiency: Results of clinical trials in Russia 1994 ·Problems of Endocrinology ·И. И. Дедов, Valentina Peterkova, Н. П. Гончаров, (unknown), О. В. Фофанова, (unknown), (unknown)	1
16	GONADOTROPIN-INDEPENDENT PRECOCIOUS PUBERTY: CLINICAL AND HORMONAL EVALUATION 1993 ·Pediatric Research ·(unknown), (unknown), Ekaterina Koledova, (unknown), (unknown), (unknown), О. В. Фофанова	16

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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