Author

Nataliya Yuskiv

Observed names: N Yuskiv, Yuskiv, Nataliya

Institutions: University of British Columbia, BC Children's Hospital

Observed institutions: Centers for Disease Control and Prevention, March of Dimes, University of British Columbia, Emory University, National Center on Birth Defects and Developmental Disabilities, Sunny Hill Health Centre for Children, BC Children's Hospital, Child and Family Research Institute, BC Children's Hospital Research Institute

OpenAlex ID: A5042249668

National estimates and race/ethnic‐specific variation of selected birth defects in the United States, 1999–2001

2006 · Mark A. Canfield, Margaret A. Honein, et al. · Birth Defects Research Part A Clinical and Molecular Teratology · 663

The Association Between Major Birth Defects and Preterm Birth

2008 · Margaret A. Honein, Russell S. Kirby, et al. · Maternal and Child Health Journal · 150

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Guanidinoacetate methyltransferase (GAMT) deficiency: Outcomes in 48 individuals and recommendations for diagnosis, treatment and monitoring

2013 · Sylvia Stockler-Ipsiroglu, Clara van Karnebeek, et al. · Molecular Genetics and Metabolism · 145

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Experiences of caregivers of children with inherited metabolic diseases: a qualitative study

2016 · Shabnaz Siddiq, Brenda J. Wilson, et al. · Orphanet Journal of Rare Diseases · 75

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The Effect of Massage Therapy on Autonomic Activity in Critically Ill Children

2014 · Ling Guan, Jean-Paul Collet, et al. · Evidence-based Complementary and Alternative Medicine · 29

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Morquio B Disease. Disease Characteristics and Treatment Options of a Distinct GLB1-Related Dysostosis Multiplex

2020 · Nataliya Yuskiv, Katsumi Higaki, et al. · International Journal of Molecular Sciences · 28

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Developments in evidence creation for treatments of inborn errors of metabolism

2020 · Sylvia Stockler‐Ipsiroglu, Beth K. Potter, et al. · Journal of Inherited Metabolic Disease · 27

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Evaluation of the quality of clinical data collection for a pan-Canadian cohort of children affected by inherited metabolic diseases: lessons learned from the Canadian Inherited Metabolic Diseases Research Network

2020 · Kylie Tingley, Monica Lamoureux, et al. · Orphanet Journal of Rare Diseases · 22

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Morquio‐B disease: Clinical and genetic characteristics of a distinct GLB1‐related dysostosis multiplex

2019 · Iman S. Abumansour, Nataliya Yuskiv, et al. · JIMD Reports · 22

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Surgical Suite to Pediatric Intensive Care Unit Handover Protocol

2014 · Tracie Northway, Gordon Krahn, et al. · Journal of Nursing Care Quality · 22

High rates of neural tube defects in Ukraine

2004 · Nataliya Yuskiv, Clark O. Andelin, et al. · Birth Defects Research Part A Clinical and Molecular Teratology · 20

Reported multivitamin consumption and the occurrence of multiple congenital anomalies

2005 · Nataliya Yuskiv, Margaret A. Honein, et al. · American Journal of Medical Genetics Part A · 17

Morquio B patient/caregiver survey: First insight into the natural course of a rare GLB1 related condition

2018 · Maria Bleier, Nataliya Yuskiv, et al. · Molecular Genetics and Metabolism Reports · 15

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Nutritional management of phenylalanine hydroxylase (PAH) deficiency in pediatric patients in Canada: a survey of dietitians’ current practices

2019 · Nataliya Yuskiv, Beth K. Potter, et al. · Orphanet Journal of Rare Diseases · 11

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Morquio‐like dysostosis multiplex presenting with neuronopathic features is a distinct GLB1 ‐related phenotype

2021 · Sylvia Stockler‐Ipsiroglu, Nahid Yazdanpanah, et al. · JIMD Reports · 9

Individualized long-term outcomes in blood phenylalanine concentrations and dietary phenylalanine tolerance in 11 patients with primary phenylalanine hydroxylase (PAH) deficiency treated with Sapropterin-dihydrochloride

2014 · Sylvia Stockler-Ipsiroglu, Nataliya Yuskiv, et al. · Molecular Genetics and Metabolism · 7

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Metabolic Control and Frequency of Clinical Monitoring Among Canadian Children With Phenylalanine Hydroxylase Deficiency: A Retrospective Cohort Study

2025 · Nataliya Yuskiv, Ammar Saad, et al. · JIMD Reports · 1

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Assessment of contrast sensitivity in children with Phenylketonuria

2021 · Yousef M Shahin, En Cheng (Kevin) Chang, et al. · Journal of Vision

Comprehensive analysis of current PKU management practices and associated patient and parent-reported outcomes in Canada

2020 · Yuskiv, Nataliya · cIRcle (University of British Columbia)

The effect of pharmacological intervention on contrast sensitivity deficits in phenylketonuria

2015 · Marcus Watson, Nataliya Yuskiv, et al. · Journal of Vision

Blood phenylalanine concentrations and dietary phenylalanine tolerance in patients with PKU in response to treatment with sapropterin hydrochloride: A multidimensional approach to determine clinically meaningful outcomes

2014 · Sylvia Stockler-Ipsiroglu, Nataliya Yuskiv, et al. · Clinical Biochemistry

Building a pan-Canadian practice-based research network for inherited metabolic diseases: The first two years of the Canadian Inherited Metabolic Diseases Research Network (CIMDRN)

2014 · Beth K. Potter, Pranesh Chakraborty, et al. · Clinical Biochemistry

460: Reported Multivitamin Consumption and Multiple Congenital Anomalies

2005 · N Yuskiv, M A Honein, et al. · American Journal of Epidemiology

Works count: 31

Citation count: 1,263

H-index: 13

I10-index: 14