H H Dahl - Concepedia

Author

H H Dahl

Also Known As

H DAHL, H H Dahl, H H M Dahl, H-H M Dahl, H-H. M. Dahl, H. -H. M. Dahl, H. H. Dahl, H. H. M. DAHL, H. H. M. Dahl, H. ‐H. M. Dahl

Publications

3.5K

Citations

H-Index

Concepts

All Affiliations

Royal Children's Hospital The University of Melbourne Australian National University The Honourable Society of Lincoln's Inn

About

H H Dahl is an author at Royal Children's Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	19	1.8K
2	Natural Sciences	9	9	465
3	Engineering	1	1	316
4	Health Sciences	1	1	11
5	Public Health	1	1	17

H H Dahl

Publications

2.9K

Citations

H-Index

Page 1

	Year	Citations
Leigh syndrome: Clinical features and biochemical and DNA abnormalities S. Rahman, Rozanne B. Blok, H H Dahl, Annals of Neurology Down SyndromeComplex Iv-deficient SibshipsGenetic TestingMendelian DisorderGenetic Disorder	1996	776
The construction of cosmid libraries which can be used to transform eukaryotic cells F Grosveld, Torben Lund, Edward J. Murray, Nucleic Acids Research EngineeringReverse GeneticsGeneticsMolecular BiologyBiological Computing	1982	316
Respiratory chain complex I deficiency Denise M. Kirby, Megan Crawford, Maureen Cleary, Neurology	1999	264
The human pyruvate dehydrogenase complex. Isolation of cDNA clones for the E1 alpha subunit, sequence analysis, and characterization of the mRNA. H H Dahl, S. M. Hunt, Wendy Hutchison, Journal of Biological Chemistry GeneticsMolecular BiologyMolecular GeneticsMitochondrial BiogenesisBiochemical Genetics	1987	142
Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis Katherine R. Smith, H H Dahl, Laura Canafoglia, Human Molecular Genetics GeneticsKufs DiseasePathologyMolecular GeneticsDisease Gene Identification	2013	127
Mitochondrial DNA mutations at nucleotide 8993 show a lack of tissue‐ or age‐related variation S. L. White, Sara Shanske, James McGill, Journal of Inherited Metabolic Disease	1999	111
Characterization of the Polypeptide Composition of Human Factor VIII:C and the Nucleotide Sequence and Expression of the Human Kidney cDNA Martha Truett, Russell Blacher, Rae Lyn Burke, DNA	1985	104
Isolation and sequence of a cDNA clone which contains the complete coding region of rat phenylalanine hydroxylase. Structural homology with tyrosine hydroxylase, glucocorticoid regulation, and use of alternate polyadenylation sites. H H Dahl, J. F. B. Mercer Journal of Biological Chemistry BiosynthesisProtein ExpressionTyrosine HydroxylaseBiochemistryCellular Enzymology	1986	89
Structure and expression of a cloned β°thalassaemic globin gene Nicholas Κ. Moschonas, Ernie de Boer, Frank Grosveld, Nucleic Acids Research	1981	85
A Frameshift Mutation Results in a Truncated Nonfunctional Carboxyl-terminal Proα1(I) Propeptide of Type I Collagen in Osteogenesis Imperfecta John F. Bateman, Shireen R. Lamandé, H H Dahl, Journal of Biological Chemistry GeneticsChemical ModificationMolecular BiologyOsteogenesisMolecular Genetics	1989	75

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