Why Kolabtree
Getting started is quick and easy. No upfront fees
It’s free to request a service and invite bids from experts
Discuss requirements with the expert in detail before accepting statement of work from Kolabtree
Collaborate with the expert directly to get your work done the right way
Fund project when you hire the expert, but approve the deliverables only once work is done
Want to hire this expert for a project? Request a quote for free.
Profile Details
Create Project
Hire Dr. Ariane S.
United Kingdom

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

Profile Summary
Subject Matter Expertise
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
Work Experience

Postdoctoral researcher - Asymmetry in priapium fishes

Natural History Museum

November 2016 - Present

Postdoctoral research fellow - Asthma

University of Bedfordshire

October 2015 - October 2016

Ebola Lab Volunteer

Public Health England

September 2015 - October 2015

Postdoctoral research fellow - Autoinflammation

University College London Institute of Child Health

September 2012 - September 2015


PhD - Genetics of Autoinflammation

University College London

October 2008 - September 2013

MSc - Integrative Biosciences

University of Oxford

October 2007 - September 2008

BA - Natural Sciences


October 2003 - June 2006

  • Certification details not provided.
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). p. 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). p. 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). p. 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). p. 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). p. 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). p. 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). p. 197-202.
Standing, A., Omoyinmi, E., Brogan, P.(2013). Gene hunting in autoinflammation . Clinical and Translational Allergy. 3. (1). p. 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). p. 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). p. 1349-1350.