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Celine Lewis

Showing results (81-90 of 88) with videos related to

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Prenatal Diagnosis|March 16, 2021
Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross-sectional study with healthcare professionalsCeline Lewis, Jennifer Hammond, Jasmijn E Klapwijk, et al.
NIHR Open Research|October 25, 2023
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocolCeline Lewis, James Buchanan, Angus Clarke, et al.
Clinical Genetics|June 22, 2021
How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policiesJasmijn E Klapwijk, Malgorzata I Srebniak, Attie T J I Go, et al.
Prenatal Diagnosis|April 27, 2022
Factors that impact on women's decision-making around prenatal genomic tests: An international discrete choice surveyJames Buchanan, Melissa Hill, Caroline M Vass, et al.
European Journal of Human Genetics : EJHG|August 22, 2025
Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementationMichael P Mackley, Pankaj B Agrawal, Sara S Ali, et al.
European Journal of Human Genetics : EJHG|September 25, 2014
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonablenessFranziska Severin, Pascal Borry, Martina C Cornel, et al.
Clinical Child Psychology and Psychiatry|May 8, 2024
"<i>People don't have the answers</i>": A qualitative exploration of the experiences of young people with Long COVIDFiona Newlands, Celine Lewis, Anais d'Oelsnitz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2025
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
Pageof 9

Showing results (81-90 of 88) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 88 results.
Prenatal Diagnosis|March 16, 2021
Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross-sectional study with healthcare professionalsCeline Lewis, Jennifer Hammond, Jasmijn E Klapwijk, et al.
NIHR Open Research|October 25, 2023
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocolCeline Lewis, James Buchanan, Angus Clarke, et al.
Clinical Genetics|June 22, 2021
How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policiesJasmijn E Klapwijk, Malgorzata I Srebniak, Attie T J I Go, et al.
Prenatal Diagnosis|April 27, 2022
Factors that impact on women's decision-making around prenatal genomic tests: An international discrete choice surveyJames Buchanan, Melissa Hill, Caroline M Vass, et al.
European Journal of Human Genetics : EJHG|August 22, 2025
Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementationMichael P Mackley, Pankaj B Agrawal, Sara S Ali, et al.
European Journal of Human Genetics : EJHG|September 25, 2014
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonablenessFranziska Severin, Pascal Borry, Martina C Cornel, et al.
Clinical Child Psychology and Psychiatry|May 8, 2024
"<i>People don't have the answers</i>": A qualitative exploration of the experiences of young people with Long COVIDFiona Newlands, Celine Lewis, Anais d'Oelsnitz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2025
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
Pageof 9