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The Finnish genetic heritage in 2022 – from diagnosis to translational research

Disease models & mechanisms, 2022-10, Vol.15 (10)

2022

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The IL-8 , VEGF , and CFH Polymorphisms and Bevacizumab in Age-related Macular Degeneration

Ophthalmology (Rochester, Minn.), 2014-04, Vol.121 (4), p.973-974.e2

2014

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Interleukin 8 promoter polymorphism predicts the initial response to bevacizumab treatment for exudative age-related macular degeneration

Retina (Philadelphia, Pa.), 2013-10, Vol.33 (9), p.1815-1827

2013

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X-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypes

Orphanet journal of rare diseases, 2014-04, Vol.9 (1), p.49-49, Article 49

2014

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Linkage and candidate gene studies of autism spectrum disorders in European populations

European journal of human genetics : EJHG, 2010-09, Vol.18 (9), p.1013-1019

2010

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Music-listening regulates human microRNA expression

Epigenetics, 2021-05, Vol.16 (5), p.554-566

2021

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Lactase persistence genotypes and malaria susceptibility in Fulani of Mali

Malaria journal, 2011-01, Vol.10 (1), p.9-9, Article 9

2011

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Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD)

BMC gastroenterology, 2009-01, Vol.9 (1), p.8-8, Article 8

2009

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Molecular Analysis of Familial Endometrial Carcinoma: A Manifestation of Hereditary Nonpolyposis Colorectal Cancer or a Separate Syndrome?

Journal of clinical oncology, 2005-07, Vol.23 (21), p.4609-4616

2005

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Analysis of four neuroligin genes as candidates for autism

European journal of human genetics : EJHG, 2005-12, Vol.13 (12), p.1285-1292

2005

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Creative Activities in Music--A Genome-Wide Linkage Analysis

PloS one, 2016-02, Vol.11 (2), p.e0148679-e0148679

2016

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Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music

PloS one, 2013-02, Vol.8 (2), p.e56356

2013

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Multifactor effects and evidence of potential interaction between complement factor H Y402H and LOC387715 A69S in age-related macular degeneration

PloS one, 2008-12, Vol.3 (12), p.e3833-e3833

2008

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Musical aptitude is associated with AVPR1A-haplotypes

PloS one, 2009-05, Vol.4 (5), p.e5534-e5534

2009

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Causes of Death of Professional Musicians in the Classical Genre

Medical problems of performing artists, 2019-06, Vol.34 (2), p.92-97

2019

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Complement factor H Y402H polymorphism and characteristics of exudative age‐related macular degeneration lesions

Acta ophthalmologica (Oxford, England), 2008-06, Vol.86 (4), p.390-394

2008

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Detecting signatures of positive selection associated with musical aptitude in the human genome

Scientific reports, 2016-02, Vol.6 (1), p.21198-21198, Article 21198

2016

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Identification of a variant associated with adult-type hypolactasia

Nature genetics, 2002-02, Vol.30 (2), p.233-237

2002

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Elevated lysosomal pH in neuronal ceroid lipofuscinoses (NCLs)

European journal of biochemistry, 2001-11, Vol.268 (22), p.5851-5856

2001

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The genetic variant rs4073 A→T of the Interleukin‐8 promoter region is associated with the earlier onset of exudative age‐related macular degeneration

Acta ophthalmologica (Oxford, England), 2015-12, Vol.93 (8), p.726-733

2015

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Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders

PLoS genetics, 2012-02, Vol.8 (2), p.e1002521

2012

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Association of the arginine vasopressin receptor 1A ( ) haplotypes with listening to music

Journal of human genetics, 2011-04, Vol.56 (4), p.324-329

2011

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Adenomatous Polyposis Families That Screen APC Mutation–Negative by Conventional Methods Are Genetically Heterogeneous

Journal of clinical oncology, 2005-08, Vol.23 (24), p.5651-5659

2005

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Lactase non-persistent genotype influences milk consumption and gastrointestinal symptoms in Northern Russians

BMC gastroenterology, 2011-11, Vol.11 (1), p.124-124, Article 124

2011

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Can primary hypolactasia manifest itself after the age of 20 years? A two-decade follow-up study

Scandinavian journal of gastroenterology, 2008, Vol.43 (9), p.1082-1087

2008

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The Finnish genetic heritage in 2022 – from diagnosis to translational research

The IL-8 , VEGF , and CFH Polymorphisms and Bevacizumab in Age-related Macular Degeneration

Interleukin 8 promoter polymorphism predicts the initial response to bevacizumab treatment for exudative age-related macular degeneration

X-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypes

Linkage and candidate gene studies of autism spectrum disorders in European populations

Music-listening regulates human microRNA expression

Lactase persistence genotypes and malaria susceptibility in Fulani of Mali

Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD)

Molecular Analysis of Familial Endometrial Carcinoma: A Manifestation of Hereditary Nonpolyposis Colorectal Cancer or a Separate Syndrome?

Analysis of four neuroligin genes as candidates for autism

Creative Activities in Music--A Genome-Wide Linkage Analysis

Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music

Multifactor effects and evidence of potential interaction between complement factor H Y402H and LOC387715 A69S in age-related macular degeneration

Musical aptitude is associated with AVPR1A-haplotypes

Causes of Death of Professional Musicians in the Classical Genre

Complement factor H Y402H polymorphism and characteristics of exudative age‐related macular degeneration lesions

Detecting signatures of positive selection associated with musical aptitude in the human genome

Identification of a variant associated with adult-type hypolactasia

Elevated lysosomal pH in neuronal ceroid lipofuscinoses (NCLs)

The genetic variant rs4073 A→T of the Interleukin‐8 promoter region is associated with the earlier onset of exudative age‐related macular degeneration

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders

Association of the arginine vasopressin receptor 1A ( ) haplotypes with listening to music

Adenomatous Polyposis Families That Screen APC Mutation–Negative by Conventional Methods Are Genetically Heterogeneous

Lactase non-persistent genotype influences milk consumption and gastrointestinal symptoms in Northern Russians

Can primary hypolactasia manifest itself after the age of 20 years? A two-decade follow-up study

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