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Author

Yuval E. Landau

Observed names: Eliahu Yuval Landau, Landau, Yuval, Y. E. Landau, Y.E. Landau, Yuval E Landau, Yuval Eliahu Landau, Yuval Landau
Observed institutions: Boston Children's Hospital, Mayo Clinic, Harvard University, Tel Aviv University, Tel Aviv Sourasky Medical Center, Sheba Medical Center, Rabin Medical Center, Rambam Health Care Campus, Schneider Children's Medical Center, Edmond and Lily Safra Children's Hospital
ORCID: 0000-0003-4420-1480
Observed ORCID: 0000-0003-4420-1480
OpenAlex ID: A5032863194
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability
2017 · Yair Anikster, Tobias B. Haack, et al. · The American Journal of Human Genetics · 162
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The natural history of classic galactosemia: lessons from the GalNet registry
2019 · M. E. Rubio-Gozalbo, M. Haskovic, et al. · Orphanet Journal of Rare Diseases · 149
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Genomics in Newborn Screening
2013 · Yuval E. Landau, Uta Lichter-Konecki, et al. · The Journal of Pediatrics · 74
Can untreated PKU patients escape from intellectual disability? A systematic review
2018 · Danique van Vliet, Annemiek M. J. van Wegberg, et al. · Orphanet Journal of Rare Diseases · 67
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Long COVID‐19 Liver Manifestation in Children
2022 · Shiri Cooper, Ana Tobar, et al. · Journal of Pediatric Gastroenterology and Nutrition · 65
DLG4-related synaptopathy: a new rare brain disorder
2021 · Agustí Rodríguez-Palmero, Melissa Maria Boerrigter, et al. · Genetics in Medicine · 60
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Pediatric Neurologic Complications Associated With Influenza A H1N1
2010 · Yuval E. Landau, Galia Grisaru-Soen, et al. · Pediatric Neurology · 53
Long‐term outcome of expanded newborn screening at Boston children's hospital: benefits and challenges in defining true disease
2017 · Yuval E. Landau, Susan E. Waisbren, et al. · Journal of Inherited Metabolic Disease · 44
Dataset Growth in Medical Image Analysis Research
2021 · Nahum Kiryati, Yuval Landau · Journal of Imaging · 42
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Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases
2017 · Asaf Vivante, Hadas Ityel, et al. · Pediatric Nephrology · 36
Neuropsychological outcomes in fatty acid oxidation disorders: 85 cases detected by newborn screening
2013 · Susan E. Waisbren, Yuval Landau, et al. · Developmental Disabilities Research Reviews · 35
Involvement of immunologic and biochemical mechanisms in the pathogenesis of Tourette’s syndrome
2011 · Yuval Eliahu Landau, Tamar Steinberg, et al. · Journal of Neural Transmission · 25
Clues and challenges in the diagnosis of intermittent maple syrup urine disease
2020 · Naomi Pode-Shakked, Stanley H. Korman, et al. · European Journal of Medical Genetics · 24
Four patients with D-bifunctional protein (DBP) deficiency: Expanding the phenotypic spectrum of a highly variable disease
2020 · Yuval E. Landau, Gali Heimer, et al. · Molecular Genetics and Metabolism Reports · 22
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Creatine transporter deficiency: Novel mutations and functional studies
2016 · O. Ardon, M. Procter, et al. · Molecular Genetics and Metabolism Reports · 21
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Reversal of cystoid macular edema in gyrate atrophy patients
2017 · Dan Heller, Chen Weiner, et al. · Ophthalmic Genetics · 20
Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants
2022 · Georg F. Vogel, Yael Mozer-Glassberg, et al. · Genetics in Medicine · 19
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The role of orotic acid measurement in routine newborn screening for urea cycle disorders
2020 · Orna Staretz‐Chacham, Suha Daas, et al. · Journal of Inherited Metabolic Disease · 18
Clinicoradiologic Criteria for the Diagnosis of Stroke-like Episodes in MELAS
2023 · Vadim Khasminsky, Eitan Auriel, et al. · Neurology Genetics · 16
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Recurrent unexplained hyperammonemia in an adolescent with arginase deficiency
2012 · Yan Zhang, Yuval E. Landau, et al. · Clinical Biochemistry · 15
Cardiac failure in very long chain acyl-CoA dehydrogenase deficiency requiring extracorporeal membrane oxygenation (ECMO) treatment: A case report and review of the literature
2016 · Sharon Katz, Yuval Landau, et al. · Molecular Genetics and Metabolism Reports · 12
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The natural history of dihydrolipoamide dehydrogenase deficiency in Israel
2024 · Ben Pode‐Shakked, Yuval E. Landau, et al. · Journal of Inherited Metabolic Disease · 11
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Management of children with nonfebrile seizures in the emergency department
2010 · Yuval E. Landau, Yehezkel Waisman, et al. · European Journal of Paediatric Neurology · 11
Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants
2023 · Georg F. Vogel, Yael Mozer-Glassberg, et al. · Genetics in Medicine · 7
Therapeutic hypothermia for asphyxiated newborns: experience of an Israeli tertiary center.
2011 · Yuval Landau, Irit Berger, et al. · PubMed · 7
Works count: 44
Citation count: 1,056
H-index: 18
I10-index: 23
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