プロフィール詳細

プロジェクトを作成

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Dr. Ariane S.に依頼

United Kingdom

Research scientist with a background in Genetics, Inflammation and Evolutionary Developmental Biology

プロフィール概要

I'm a researcher interested in how transformations at the genetic level translates to changes in functions at the protein, cellular and organismal levels. This has lead me to work on a range of projects: from the genetics and pathogenesis of autoinflammatory diseases at the UCL and Great Ormond St Institute of Child Health, the role of morphogens in asthma, to developmental biology and evolutionary novelty in unique and unusual fishes at the Natural History Museum London. I have experience writing manuscripts and presentations and peer reviewing for journals. I also have experience in science communication and education, and I am a Fellow of the Higher Education Academy.

専門分野

• ★ Next Generation Sequencing (NGS)
• ★ Immunogenetics
• ☆ Developmental Biology
• ☆ Evolutionary Biology
• ☆ Animal Genetics
• ☆ Molecular Biology
• ☆ Genetics
• ☆ Cell Signaling Pathways
• ☆ Genetic Engineering
• ☆ Phylogenetics
• ☆ Science Education
• ☆ Medicine
• ☆ Medical Genetics
• ☆ Gene Therapy
• ☆ Inflammation
• ☆ Medical Writing
• ☆ Science Communication

サービス

• Writing
• Research
• Data & AI

Writing Clinical Trial Documentation, Technical Writing, Newswriting

Research Fact Checking, Gray Literature Search, Systematic Literature Review, Secondary Data Collection

Data & AI Statistical Analysis, Data Visualization

職務経験

Postdoctoral researcher - Asymmetry in priapium fishes

Natural History Museum

11月 2016 - 現在

Postdoctoral research fellow - Asthma

University of Bedfordshire

10月 2015 - 10月 2016

Ebola Lab Volunteer

Public Health England

9月 2015 - 10月 2015

Postdoctoral research fellow - Autoinflammation

University College London Institute of Child Health

9月 2012 - 9月 2015

学歴

PhD - Genetics of Autoinflammation

University College London

10月 2008 - 9月 2013

MSc - Integrative Biosciences

University of Oxford

10月 2007 - 9月 2008

BA - Natural Sciences

UNIVERSITY OF CAMBRIDGE

10月 2003 - 6月 2006

認定資格

• 認定資格の詳細は未入力です。

出版物

JOURNAL ARTICLE

Hong, Y., Standing, A.S.I., Nanthapisal, S., Sebire, N., Jolles, S., Omoyinmi, E., Verstegen, R.H., Brogan, P.A., Eleftheriou, D.(2019). Autoinflammation due to homozygous S208 MEFV mutation . Annals of the Rheumatic Diseases. 78. (4). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 571-573.

Papadopoulou, C., Omoyinmi, E., Standing, A., Pain, C.E., Booth, C., D'Arco, F., Gilmour, K., Buckland, M., Eleftheriou, D., Brogan, P.A.(2019). Monogenic mimics of Behçet's disease in the young . Rheumatology (United Kingdom). 58. (7). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 1227-1238.

De Benedetti F, Anton J, Gattorno M, Lachmann H, Kone-Paut I, Ozen S, Frenkel J, Simon A, Zeft A, Ben-Chetrit E, et al.(2017). Proceedings of the 23 Paediatric Rheumatology European Society Congress: part one: Genoa . Pediatric rheumatology online journal.

Omoyinmi, E., Standing, A., Keylock, A., Price-Kuehne, F., Melo Gomes, S., Rowczenio, D., Nanthapisal, S., Cullup, T., Nyanhete, R., Ashton, E., et al.(2017). Clinical impact of a targeted next-generation sequencing gene panel for autoinflammation and vasculitis . PLoS ONE. 12. (7).

Standing, A.S.I., Yánez, D.C., Ross, R., Crompton, T., Furmanski, A.L.(2017). Frontline science: Shh production and Gli signaling is activated in vivo in lung, enhancing the Th2 response during a murine model of allergic asthma . Journal of Leukocyte Biology. 102. (4). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 965-976.

Standing, A.S.I., Malinova, D., Hong, Y., Record, J., Moulding, D., Blundell, M.P., Nowak, K., Jones, H., Omoyinmi, E., Gilmour, K.C., et al.(2017). Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actinregulatory gene WDR1 . Journal of Experimental Medicine. 214. (1). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 59-71.

Nanthapisal, S., Omoyinmi, E., Murphy, C., Standing, A., Eisenhut, M., Eleftheriou, D., Brogan, P.A.(2017). Early-onset juvenile SLE associated with a novel mutation in protein kinase C δ . Pediatrics. 139. (1).

Nanthapisal, S., Murphy, C., Omoyinmi, E., Hong, Y., Standing, A., Berg, S., Ekelund, M., Jolles, S., Harper, L., Youngstein, T., et al.(2016). Deficiency of Adenosine Deaminase Type 2: A Description of Phenotype and Genotype in Fifteen Cases . Arthritis and Rheumatology. 68. (9). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 2314-2322.

Nanthapisal S, Murphy C, Omoyinmi E, Standing A, Hong Y, Gomes S, Klein N, Eleftheriou D, Brogan P(2015). Monogenic polyarteritis nodosa caused by ADA2 Deficiency: the GOSH experience . Pediatric rheumatology online journal.

Standing, A., Eleftheriou, D., Paisan-Ruiz, C., Rowcenzio, D., Hong, Y., Omoyinmi, E., Woo, P., Hawkins, P., Lachmann, H., Klein, N., et al.(2015). Loss of function mutation in a mitochondrial chaperone protein leading to dyregulated ROS production, and autoinflammatory disease in a single kindred . Pediatric Rheumatology. 13. (1).

Standing, A., Malinova, D., Record, J., Moulding, D., Blundell, M., Nowak, K., Jones, H., Omoyinmi, E., Nanthapisal, S., Gomes, S.M., et al.(2015). Severe autoinflammatory disease caused by mutation in a gene controlling actin cytoskeletal dynamics and cure with allogeneic haematopoetic stem cell transplantation . Pediatric Rheumatology. 13. (1).

Omoyinmi, E., Melo Gomes, S., Nanthapisal, S., Woo, P., Standing, A., Eleftheriou, D., Klein, N., Brogan, P.A.(2015). Stimulator of interferon genes-associated vasculitis of infancy . Arthritis and Rheumatology. 67. (3). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 808.

Rowczenio, D., Gomes, S.M., Aróstegui, J., Omoyinmi, E., Gonzalez-Roca, E., Standing, A., Eleftheriou, D., Klein, N., Brogan, P., Lachmann, H., et al.(2015). Late onset of the cryopyrin-associated periodic syndrome (CAPS) associated with low level of somatic mosaicism in six patients . Pediatric Rheumatology. 13. (1).

Gomes, S.M., Arostegui, J., Omoyinmi, E., Standing, A., Klein, N., Lachmann, H., Hawkins, P., Brogan, P.(2015). Whole Exome Sequencing reveals a NLRP3 mutation in exon 5 in a patient with CINCA . Pediatric Rheumatology. 13. (1).

Standing A, Paisan-Ruiz C, Eleftheriou D, Hong Y, Omoyinmi E, Rowcenzio D, Lachmann H, Hawkins P, Woo P, Klein N, et al.(2014). Identification of a novel monogenic autoinflammatory disease due to mutation in a mitochondrial chaperone protein in a single kindred, and cure with allogeneic haematopoietic stem cell transplantation . Pediatric rheumatology online journal.

Gomes SM, Arostegui J, Omonyinmi E, Gonzalez-Roca E, Standing A, Rowczenio D, Nathanpisal S, Murphy C, Elephteriou D, Klein N, et al.(2014). The role of somatic NLRP3 mosaicism and new gene discovery in mutation negative cryopyrin-associated periodic syndrome patients . Pediatric rheumatology online journal.

Omoyinmi, E., Gomes, S.M., Standing, A., Rowczenio, D.M., Eleftheriou, D., Klein, N., Aróstegui, J.I., Lachmann, H.J., Hawkins, P.N., Brogan, P.A.(2014). Whole-exome sequencing revealing somatic NLRP3 mosaicism in a patient with chronic infantile neurologic, cutaneous, articular syndrome . Arthritis and Rheumatology. 66. (1). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 197-202.

Standing, A., Omoyinmi, E., Brogan, P.(2013). Gene hunting in autoinflammation . Clinical and Translational Allergy. 3. (1). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 1-7.

Standing, A.S.I., Eleftheriou, D., Lachmann, H.J., Brogan, P.A.(2011). Familial Mediterranean fever caused by homozygous E148Q mutation complicated by Budd-Chiari syndrome and polyarteritis nodosa . Rheumatology. 50. (3). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 624-626.

Standing, A.S.I., Eleftheriou, D., Lachmann, H.J., Brogan, P.A.(2011). Comment on: Familial Mediterranean fever caused by homozygous E148Q mutation complicated by Budd-Chiari syndrome and polyarteritis nodosa: Reply . Rheumatology. 50. (7). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 1349-1350.