Yolanda Lillquist

Statistics

Publications

Citations

372

H-Index

Active since

2004

Affiliations

Children's & Women's Health Centre of British Columbia(Current)

BC Children's Hospital

University of British Columbia

University Children's Hospital Zurich

Sheffield Children's Hospital

Yolanda Lillquist is an author at Children's & Women's Health Centre of British Columbia specializing in medicine, pediatrics, and molecular genetics.

Publications per year

2004–2015

Publications

CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder

Saskia B. Wortmann, Szymon Ziętkiewicz, Maria Kousi et al. · The American Journal of Human Genetics · 2015 · 135 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populations

Cheryl R. Greenberg, Louise A. Dilling, Gilbert R. Thompson et al. · Molecular Genetics and Metabolism · 2009 · 79 citations

Life Sciences, Molecular Biology, Molecular Genetics +4

Autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia: Evidence of a phenotypic continuum between dominant and recessive forms

Gabriella Horváth, Sylvia Stöckler‐Ipsiroglu, Ramona Salvarinova et al. · Molecular Genetics and Metabolism · 2008 · 44 citations

Life Sciences, Genetics, Molecular Genetics +11

Newborn Screening for MCAD Deficiency

Gabriella Horváth, A. George F. Davidson, Sylvia Stöckler‐Ipsiroglu et al. · Canadian Journal of Public Health · 2008 · 27 citations · Full text

Medicine, Child Health, Pediatrics +13

Carnitine transporter defect due to a novel mutation in the <i>SLC22A5</i> gene presenting with peripheral neuropathy

Nawal Makhseed, Hilary Vallance, Murray Potter et al. · Journal of Inherited Metabolic Disease · 2004 · 23 citations

Medicine, Genetics, Molecular Genetics +12

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