Elizabeth Ives - Concepedia

Author

Elizabeth Ives

Also Known As

E Ives, E J Ives, E. Ives, E. J. Ives, E.J. Ives, Elizabeth Ives, Elizabeth J Ives, Elizabeth J. Ives, Elizabeth J. Ives

Publications

2.5K

Citations

H-Index

Concepts

All Affiliations

Memorial University of Newfoundland University of Alberta University of British Columbia University of Saskatchewan National Institutes of Health

About

Elizabeth Ives is an author at Memorial University of Newfoundland specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	892
2	Public Health	2	2	485
3	Health Sciences	1	1	66
4	Natural Sciences	1	1	41
5	Biology	1	1	41

Elizabeth Ives

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm Håkan Telenius, Berry Kremer, Y. Paul Goldberg, Nature Genetics SpermatogenesisGenetic DisorderGeneticsGameteMolecular Genetics	1994	449
Loss‐of‐function mutations in the Na <sub>v</sub> 1.7 gene underlie congenital indifference to pain in multiple human populations Y. Paul Goldberg, Julie MacFarlane, ML MacDonald, Clinical Genetics	2007	448
Smith‐Lemli‐Opitz syndrome‐type II: Multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality Cynthia J. Curry, John C. Carey, Julie Holland, American Journal of Medical Genetics	1987	230
Risk modifiers in carriers of brca1 mutations Steven A. Narod, David E. Goldgar, Lisa Cannon‐Albright, International Journal of Cancer	1995	164
A transcriptional insulator at the imprinted <i>H19/Igf2</i> locus Christopher R. Kaffer, M. P. Srivastava, Kyeyoon Park, Genes & Development	2000	149
Contribution of DNA Sequence and CAG Size to Mutation Frequencies of Intermediate Alleles for Huntington Disease: Evidence from Single Sperm Analyses Samuel S. Chong, E. Almqvist, H. Telenius, Human Molecular Genetics	1997	120
The clinical and genetic epidemiology of neuronal ceroid lipofuscinosis in Newfoundland S. Jo Moore, DJ Buckley, A. MacMillan, Clinical Genetics	2008	80
Sorsby's fundus dystrophy is genetically linked to chromosome 22q13–qter Bernhard H. F. Weber, Gudrun Vogt, W. Wolz, Nature Genetics Fundus DystrophyMendelian DisorderGenetic DisorderGeneticsDegenerative Disease	1994	79
The abdominal muscle deficiency triad syndrome--experience with ten cases. Elizabeth Ives PubMed Muscle DisordersDevelopmental AnomalyRare DiseasesGross AnatomyEndocrine Disease	1974	66
VAMP1 Mutation Causes Dominant Hereditary Spastic Ataxia in Newfoundland Families Cynthia V. Bourassa, Inge A. Meijer, Nancy D. Merner, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyNewfoundland Families	2012	54

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