Concepedia

Tiina Alitalo

TA

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Publications

27

Citations

1.2K

H-Index

23

Active since

1987

Affiliations

University of Helsinki(Current)

Helsinki University Hospital

Folkhälsans Forskningscentrum

Kuopio University Hospital

The Ohio State University

Tiina Alitalo is an author at University of Helsinki specializing in genetics, molecular genetics, and life sciences.

Publications per year

1987–2021

27

Publications

27

X-Linked Cone-Rod Dystrophy (Locus COD1): Identification of Mutations in RPGR Exon ORF15

F. Yesim Demirci, Brian W. Rigatti, Gaiping Wen et al. · The American Journal of Human Genetics · 2002 · 169 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

A locus for autosomal dominant keratoconus: linkage to 16q22.3-q23.1 in Finnish families.

Henna Tyynismaa, Pertti Sistonen, Sari Tuupanen et al. · PubMed · 2002 · 151 citations

Life Sciences, Genetics, Ophthalmology +17

Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina

Krisztina Wutz, Christian Sauer, Eberhart Zrenner et al. · European Journal of Human Genetics · 2002 · 85 citations

Medicine, Genetics, Molecular Genetics +10

A Novel<i>CACNA1F</i>Gene Mutation Causes Aland Island Eye Disease

Reetta Jalkanen, N. Torben Bech‐Hansen, Rose Tobias et al. · Investigative Ophthalmology & Visual Science · 2007 · 60 citations

Medicine, Genetics, Ophthalmology +15

Prevalence of the fragile X syndrome in four birth cohorts of children of school age

Marketta K�hk�nen, Tiina Alitalo, E.M. Airaksinen et al. · Human Genetics · 1987 · 59 citations

Public Health, Genetics, Pediatrics +11

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