Hans‐Henrik M. Dahl

Author

Hans‐Henrik M. Dahl

Royal Children's Hospital

Also Known As

Hans-Henrik Dahl, Hans-Henrik M Dahl, Hans-Henrik M. Dahl, Hans‐Henrik M. Dahl

Publications

3.3K

Citations

H-Index

Concepts

All Affiliations

Royal Children's Hospital The University of Melbourne Murdoch Children's Research Institute La Trobe University Walter and Eliza Hall Institute of Medical Research

About

Hans‐Henrik M. Dahl is an author at Royal Children's Hospital specializing in genetics, medicine, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	15	1.9K
2	Arts	4	4	1.1K
3	Natural Sciences	4	4	288
4	Health Sciences	1	1	22
5	Public Health	1	1	27

Hans‐Henrik M. Dahl

Publications

3.2K

Citations

H-Index

Page 1

	Year	Citations
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann, The American Journal of Human Genetics Genetic DisorderGeneticsAudiologyGenetic EpidemiologyGjb2 Mutations	2005	551
A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes Lynsey Cree, David C. Samuels, Susana M. Chuva de Sousa Lopes, Nature Genetics Developmental BiologyRapid SegregationCell DivisionMitochondrial FunctionMedicine	2008	505
Strikingly Different Clinicopathological Phenotypes Determined by Progranulin-Mutation Dosage Katherine R. Smith, John A. Damiano, Silvana Franceschetti, The American Journal of Human Genetics Neurodegenerative DiseasesMendelian DisorderGenetic DisorderExome SequencingGenetics	2012	479
Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study Ignacio del Castillo, Miguel A. Moreno‐Pelayo, Francisco Castillo, The American Journal of Human Genetics Genetic DisorderGeneticsGenetic EpidemiologyAudiologyEvolutionary Origins	2003	289
High frequency hearing loss correlated with mutations in the GJB2 gene Stephen Wilcox, Kerryn Saunders, Amelia H. Osborn, Human Genetics Genetic DisorderGeneticsAudiologyArtsAuditory Physiology	2000	209
NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency Denise M. Kirby, Renato Salemi, Canny Sugiana, Journal of Clinical Investigation	2004	186
Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease Canny Sugiana, David J. Pagliarini, Matthew McKenzie, The American Journal of Human Genetics Genome InstabilityMitochondrial FunctionMedicineGeneticsMolecular Biology	2008	177
Skewed Segregation of the mtDNA nt 8993 (TrG) Mutation in Human Oocytes Rozanne B. Blok, Debra A. Gook, David R. Thorburn, The American Journal of Human Genetics ChromatinGenome InstabilityDnaCytogeneticsNatural Sciences	1997	175
Slight/Mild Sensorineural Hearing Loss in Children Melissa Wake, Sherryn Tobin, Barbara Cone‐Wesson, PEDIATRICS	2006	153
Etiology and Audiological Outcomes at 3 Years for 364 Children in Australia Hans‐Henrik M. Dahl, Teresa Y. C. Ching, Wendy Hutchison, PLoS ONE Genetic TestingPediatric AudiologyGeneticsGenetic EpidemiologyPathology	2013	65

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