Literature DB >> 6941915

Genetic markers in Finland.

H R Nevanlinna.   

Abstract

The number of new monogenic markers found in Finland that are unknown or very rare in other European populations is increasing almost every year. In addition, a large number of rare recessive diseases similarly typical for the Finns have been found during the last two decades. All these rare genes have probably been accumulated by chance among the numerically limited early settlers during the slow immigration to Finland. The distribution of the more common, polymorphic markers among Finns however reflects rather strong eastern influence judging from the resemblance to Estonians and Siberian populations.

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Year:  1980        PMID: 6941915

Source DB:  PubMed          Journal:  Haematologia (Budap)        ISSN: 0017-6559


  5 in total

1.  Finnish Disease Heritage II: population prehistory and genetic roots of Finns.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

2.  Multiple sclerosis in Finland: incidence trends and differences in relapsing remitting and primary progressive disease courses.

Authors:  M-L Sumelahti; P J Tienari; M Hakama; J Wikström
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-01       Impact factor: 10.154

3.  Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysis.

Authors:  T Zerjal; B Dashnyam; A Pandya; M Kayser; L Roewer; F R Santos; W Schiefenhövel; N Fretwell; M A Jobling; S Harihara; K Shimizu; D Semjidmaa; A Sajantila; P Salo; M H Crawford; E K Ginter; O V Evgrafov; C Tyler-Smith
Journal:  Am J Hum Genet       Date:  1997-05       Impact factor: 11.025

Review 4.  Disease gene mapping in isolated human populations: the example of Finland.

Authors:  A de la Chapelle
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

5.  Whole exome sequencing in Finnish families identifies new candidate genes for osteoarthritis.

Authors:  Sini Skarp; Olli-Pekka Kämäräinen; Gong-Hong Wei; Eveliina Jakkula; Ilkka Kiviranta; Heikki Kröger; Juha Auvinen; Petri Lehenkari; Leena Ala-Kokko; Minna Männikkö
Journal:  PLoS One       Date:  2018-08-29       Impact factor: 3.240

  5 in total

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