Concepedia

Author

Håkan Telenius

University of Cambridge

Also Known As

H Telenius, Hakan Telenius, HÅKan Telenius, Hâkan Telenius, Håkan Telenius

18

Publications

5.6K

Citations

13

H-Index

22

Concepts

All Affiliations

University of CambridgeUniversity of British ColumbiaKarolinska InstitutetCancer Research UK Cambridge CenterKarolinska University Hospital
HT

About

Håkan Telenius is an author at University of Cambridge specializing in medicine, genetics, and molecular genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

6

6

3.9K

2

Molecular Genetics

4

4

1.9K

3

Molecular Biology

2

2

1.4K

4

Public Health

1

1

449

5

Biology

1

1

81

Håkan Telenius

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13

Publications

5.5K

Citations

12

H-Index

YearCitations

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A

Lois M. Mulligan, John B. Kwok, Catherine S. Healey,

Nature

1993

2K

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

Susan E. Andrew, Y. Paul Goldberg, Berry Kremer,

Nature Genetics

1993

1.1K

A Worldwide Study of the Huntington's Disease Mutation: The Sensitivity and Specificity of Measuring CAG Repeats

Berry Kremer, Paul Goldberg, Susan E. Andrew,

New England Journal of Medicine

1994

587

Cytogenetic analysis by chromosome painting using dop‐pcr amplified flow‐sorted chromosomes

Håkan Telenius, Bruce A.J. Ponder, Alan Tunnacliffe,

Genes Chromosomes and Cancer

1992

576

Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm

Håkan Telenius, Berry Kremer, Y. Paul Goldberg,

Nature Genetics

1994

449

Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects

Y. Paul Goldberg, Berry Kremer, Susan E. Andrew,

Nature Genetics

1993

245

Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization

Elisabeth Blennow, Karen Brøndum Nielsen, Håkan Telenius,

American Journal of Medical Genetics

1995

155

Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population

Y. Paul Goldberg, Cynthia T. McMurray, Jutta Zeisier,

Human Molecular Genetics

1995

130

Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2

Emily Gardner, Laura Papi, Douglas F. Easton,

Human Molecular Genetics

1993

90

Chromosome 2-specific DNA clones from flow-sorted chromosomes of tomato

K. Arumuganathan, Gregory B. Martin, Håkan Telenius,

Molecular and General Genetics MGG

1994

81

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