H Kääriäinen - Concepedia

Author

H Kääriäinen

Also Known As

H KAARIAINEN, H Kaariainen, H Kääriäinen, H. Kaariainen, H. Kääriäinen, H. Kääriäinen, Helena A. Kääriäinen, Helena Kääriäinen, Kääriäinen, H.

Publications

3.4K

Citations

H-Index

Concepts

All Affiliations

University of Helsinki Väestöliitto University of Turku Helsinki Children's Hospital Finnish Institute for Health and Welfare

About

H Kääriäinen is an author at University of Helsinki specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	16	1.1K
2	Public Health	4	4	174
3	Arts	1	1	27
4	Social Sciences	1	1	28
5	Allergy	1	1	89

H Kääriäinen

Publications

3.1K

Citations

H-Index

Page 1

	Year	Citations
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. Alan H. Beggs, Mary B. Moyer, S. Scherpf, PubMed	1989	961
Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21–cen Klaus Zerres, Gabi Mücher, L Bachner, Nature Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsRenal Pathology	1994	258
Cancer in Patients With Ataxia-Telangiectasia and in Their Relatives in the Nordic Countries Jørgen H. Olsen, Johanne M D Hahnemann, A.L. Børresen-Dale, JNCI Journal of the National Cancer Institute	2001	239
A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10 Stanislas Lyonnet, Alessandra Bolino, Anna Pelet, Nature Genetics ChromatinDevelopmental BiologyCytogeneticsGenetic DisorderGenetics	1993	192
Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q Eeva‐Marja Sankila, Leenamaija Pakarinen, H Kääriäinen, Human Molecular Genetics	1995	185
Genetic Control of Serum IgE Levels and Asthma: Linkage and Linkage Disequilibrium Studies in an Isolated Population Tarja Laitinen, Paula Kauppi, Jaakko Ignatius, Human Molecular Genetics AsthmaInflammatory Lung DiseaseGeneticsImmunologyGenetic Epidemiology	1997	89
Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy) Jarmo Körkkö, Pertti Ritvaniemi, Leena Haataja, PubMed	1993	80
Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy Joyce Harper, J.P.M. Geraedts, Pascal Borry, Human Reproduction	2014	79
Long-Term Prognosis of Haemangioblastoma of the CNS: Impact of von Hippel-Lindau Disease Mika Niemelä, Sebsebe Lemeta, Paula Summanen, Acta Neurochirurgica Neuro-oncologySurgical PathologyHematologyPathologyNeurology	1999	77
Gene deletions in X-linked muscular dystrophy. Mikael Lindlöf, A Kiuru, H Kääriäinen, PubMed	1989	74

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