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Yelena Bykhovskaya

Yelena Bykhovskaya,University of California Los Angeles,Genetics & Genealogy,Molecular Biology,Biophysics

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Yelena Bykhovskaya

University of California Los Angeles

Publications: 22 | Citations: 500

Fields: Genetics & Genealogy, Molecular Biology, Biophysics

Collaborated with 77 co-authors from 1998 to 2009 | Cited by 1284 authors

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Publications (22)

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Phenotypic expression of maternally inherited deafness is affected by RNA modification and cytoplasmic ribosomal proteins (Citations: 1)

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Journal: Molecular Genetics and Metabolism - MOL GENET METAB , vol. 97, no. 4, pp. 297-304, 2009

Pleiotropic effects and compensation mechanisms determine tissue specificity in mitochondrial myopathy and sideroblastic anemia (MLASA) (Citations: 5)

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Journal: Molecular Genetics and Metabolism - MOL GENET METAB , vol. 91, no. 2, pp. 148-156, 2007

Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations (Citations: 47)

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Journal: American Journal of Human Genetics - AMER J HUM GENET , vol. 79, no. 2, pp. 291-302, 2006

Human TRMU encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase is a putative nuclear modifier gene for the phenotypic expression of the deafness-associated 12S rRNA mutations (Citations: 11)

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Journal: Biochemical and Biophysical Research Communications - BIOCHEM BIOPHYS RES COMMUN , vol. 342, no. 4, pp. 1130-1136, 2006

Mitochondrial Myopathy, Sideroblastic Anemia, and Lactic Acidosis: An Autosomal Recessive Syndrome in Persian Jews Caused by a Mutation in the PUS1 Gene (Citations: 11)

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Journal: Journal of Child Neurology - JCN , vol. 20, no. 5, pp. 449-452, 2005

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Citations (500 times by 315 publications)

Biochemical diagnosis of mitochondrial disorders (Citations: 5)

Journal: Journal of Inherited Metabolic Disease - J INHERIT METAB DIS , vol. 34, no. 2, pp. 283-292, 2011

Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation (Citations: 2)

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Journal: Mitochondrion , vol. 11, no. 1, pp. 70-75, 2011

A history of mitochondrial diseases (Citations: 2)

Journal: Journal of Inherited Metabolic Disease - J INHERIT METAB DIS , vol. 34, no. 2, pp. 261-276, 2011

Mitochondrial–nuclear epistasis: Implications for human aging and longevity (Citations: 1)

Journal: Ageing Research Reviews - AGEING RES REV , vol. 10, no. 2, pp. 238-252, 2011

A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population

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Journal: BMC Medical Genetics - BMC MED GENET , vol. 12, no. 1, pp. 1-6, 2011

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Co-authors (77)

Journals (11)

Keywords (82)

Yelena Bykhovskaya,University of California Los Angeles,Genetics & Genealogy,Molecular Biology,Biophysics

Publications (22)

BibTeX | RIS | RefWorks Download

Phenotypic expression of maternally inherited deafness is affected by RNA modification and cytoplasmic ribosomal proteins (Citations: 1)

Pleiotropic effects and compensation mechanisms determine tissue specificity in mitochondrial myopathy and sideroblastic anemia (MLASA) (Citations: 5)

Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations (Citations: 47)

Human TRMU encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase is a putative nuclear modifier gene for the phenotypic expression of the deafness-associated 12S rRNA mutations (Citations: 11)

Mitochondrial Myopathy, Sideroblastic Anemia, and Lactic Acidosis: An Autosomal Recessive Syndrome in Persian Jews Caused by a Mutation in the PUS1 Gene (Citations: 11)

Citations (500 times by 315 publications)

Biochemical diagnosis of mitochondrial disorders (Citations: 5)

Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation (Citations: 2)

A history of mitochondrial diseases (Citations: 2)

Mitochondrial–nuclear epistasis: Implications for human aging and longevity (Citations: 1)

A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population


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Co-authors (77)

Journals (11)

Keywords (82)

Yelena Bykhovskaya,University of California Los Angeles,Genetics & Genealogy,Molecular Biology,Biophysics

Publications (22) BibTeX | RIS | RefWorks Download

Phenotypic expression of maternally inherited deafness is affected by RNA modification and cytoplasmic ribosomal proteins (Citations: 1)

Pleiotropic effects and compensation mechanisms determine tissue specificity in mitochondrial myopathy and sideroblastic anemia (MLASA) (Citations: 5)

Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations (Citations: 47)

Human TRMU encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase is a putative nuclear modifier gene for the phenotypic expression of the deafness-associated 12S rRNA mutations (Citations: 11)

Mitochondrial Myopathy, Sideroblastic Anemia, and Lactic Acidosis: An Autosomal Recessive Syndrome in Persian Jews Caused by a Mutation in the PUS1 Gene (Citations: 11)

Citations (500 times by 315 publications)

Biochemical diagnosis of mitochondrial disorders (Citations: 5)

Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation (Citations: 2)

A history of mitochondrial diseases (Citations: 2)

Mitochondrial–nuclear epistasis: Implications for human aging and longevity (Citations: 1)

A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population

Publications (22)

BibTeX | RIS | RefWorks Download