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Susan Walker

Showing results (191-200 of 260) with videos related to

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Paediatric & Neonatal Pain|July 7, 2025
Nationwide Cross-Sectional Online Survey of Australian Clinicians' Pain Management Practices for Newborns During Heel Lance ProceduresSophie Jones, Nicole Pope, Margaret Broom, et al.
American Journal of Respiratory and Critical Care Medicine|January 13, 2022
Hereditary Mucin Deficiency Caused by Biallelic Loss of Function of <i>MUC5B</i>Gregory Costain, Zhen Liu, Vito Mennella, et al.
Psychological Assessment|October 13, 2022
Measuring antenatal depressive symptoms across the world: A validation and cross-country invariance analysis of the Patient Health Questionnaire-9 (PHQ-9) in eight diverse low-resource settingsAja Louise Murray, Chad Lance Hemady, Huyen Do, et al.
Annals of Neurology|September 17, 2014
Absent CNKSR2 causes seizures and intellectual, attention, and language deficitsAndrea K Vaags, Sarah Bowdin, Mary-Lou Smith, et al.
Journal of the Royal Society of New Zealand|October 23, 2024
Climate change adaptation through an integrative lens in Aotearoa New ZealandJudy Lawrence, Anita Wreford, Paula Blackett, et al.
European Journal of Human Genetics : EJHG|February 18, 2018
Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testingGregory Costain, Rebekah Jobling, Susan Walker, et al.
Archives of Women'S Mental Health|April 14, 2022
Perceived stress during the prenatal period: assessing measurement invariance of the Perceived Stress Scale (PSS-10) across cultures and birth parityLaura Katus, Sarah Foley, Aja L Murray, et al.
Journal of Medical Genetics|October 26, 2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disabilityAlistair T Pagnamenta, Hameed Khan, Susan Walker, et al.
Cell Reports|November 10, 2016
DIXDC1 Phosphorylation and Control of Dendritic Morphology Are Impaired by Rare Genetic VariantsVickie Kwan, Durga Praveen Meka, Sean H White, et al.
Human Mutation|April 14, 2025
A Palindrome-Like Structure on 16p13.3 Is Associated with the Formation of Complex Structural Variations and <i>SRRM2</i> HaploinsufficiencyAlistair T Pagnamenta, Jing Yu, Tracey A Willis, et al.
Pageof 26

Showing results (191-200 of 260) with videos related to

Sort By:
Pageof 26
Paediatric & Neonatal Pain|July 7, 2025
Nationwide Cross-Sectional Online Survey of Australian Clinicians' Pain Management Practices for Newborns During Heel Lance ProceduresSophie Jones, Nicole Pope, Margaret Broom, et al.
American Journal of Respiratory and Critical Care Medicine|January 13, 2022
Hereditary Mucin Deficiency Caused by Biallelic Loss of Function of <i>MUC5B</i>Gregory Costain, Zhen Liu, Vito Mennella, et al.
Psychological Assessment|October 13, 2022
Measuring antenatal depressive symptoms across the world: A validation and cross-country invariance analysis of the Patient Health Questionnaire-9 (PHQ-9) in eight diverse low-resource settingsAja Louise Murray, Chad Lance Hemady, Huyen Do, et al.
Annals of Neurology|September 17, 2014
Absent CNKSR2 causes seizures and intellectual, attention, and language deficitsAndrea K Vaags, Sarah Bowdin, Mary-Lou Smith, et al.
Journal of the Royal Society of New Zealand|October 23, 2024
Climate change adaptation through an integrative lens in Aotearoa New ZealandJudy Lawrence, Anita Wreford, Paula Blackett, et al.
European Journal of Human Genetics : EJHG|February 18, 2018
Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testingGregory Costain, Rebekah Jobling, Susan Walker, et al.
Archives of Women'S Mental Health|April 14, 2022
Perceived stress during the prenatal period: assessing measurement invariance of the Perceived Stress Scale (PSS-10) across cultures and birth parityLaura Katus, Sarah Foley, Aja L Murray, et al.
Journal of Medical Genetics|October 26, 2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disabilityAlistair T Pagnamenta, Hameed Khan, Susan Walker, et al.
Cell Reports|November 10, 2016
DIXDC1 Phosphorylation and Control of Dendritic Morphology Are Impaired by Rare Genetic VariantsVickie Kwan, Durga Praveen Meka, Sean H White, et al.
Human Mutation|April 14, 2025
A Palindrome-Like Structure on 16p13.3 Is Associated with the Formation of Complex Structural Variations and <i>SRRM2</i> HaploinsufficiencyAlistair T Pagnamenta, Jing Yu, Tracey A Willis, et al.
Pageof 26