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242: Profiling Multigenetic Variation in Androgen Pathway as a Risk Factor for Prostate Cancer

The Journal of urology, 2005-04, Vol.173 (4), p.66-67

2005

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251P Characteristics and overall survival of an advanced breast cancer cohort in Finland

Annals of oncology, 2020-09, Vol.31, p.S340-S340

2020

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825 Exome Sequencing of T-LGL Leukemia Patient Revealed ANGPT2 as a Possible Mutational Target

European journal of cancer (1990), 2012-07, Vol.48, p.S198-S198

2012

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A6.02 Somatic mutations in clonally expanded CD8+ T cells in patients with newly diagnosed rheumatoid arthritis

Annals of the rheumatic diseases, 2016-02, Vol.75 (Suppl 1), p.A47-A48

2016

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Abstract 606: Novel somatic mutations in the DNA-binding and coiled-coil domain of the STAT3 gene in LGL-leukemia

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.606-606

2015

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Acquired Somatic Mutations in T Cells in Patients with Aplastic Anemia and Hypoplastic Myelodysplastic Syndromes

Blood, 2017-12, Vol.130, p.1169-1169

2017

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Activating somatic mutations outside the SH2-domain of STAT3 in LGL leukemia

Leukemia, 2016-05, Vol.30 (5), p.1204-1208

2016

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ALWAYS THE LITTLE BROTHER? DIGITAL-PRODUCT INNOVATION IN THE MEDIA SECTOR

International journal of innovation and technology management, 2006-03, Vol.3 (1), p.83-105

2006

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The analysis of clonal diversity and therapy responses using STAT3 mutations as a molecular marker in large granular lymphocytic leukemia

Haematologica (Roma), 2015-01, Vol.100 (1), p.91-99

2015

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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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Association of a Nonsynonymous Variant of DAOA with Visuospatial Ability in a Bipolar Family Sample

Biological psychiatry (1969), 2008-09, Vol.64 (5), p.438-442

2008

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Case studies investigating genetic heterogeneity between anatomically distinct bone marrow compartments in acute myeloid leukemia

Leukemia & lymphoma, 2018-12, Vol.59 (12), p.3002-3005

2018

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Chromosome 1 loci in finnish schizophrenia families

Human molecular genetics, 2001-07, Vol.10 (15), p.1611-1617

2001

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Copy number alterations and neoplasia-specific mutations in MELK, PDCD1LG2, TLN1, and PAX5 at 9p in different neoplasias

Genes chromosomes & cancer, 2014-07, Vol.53 (7), p.579-588

2014

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Development of SNP microarray for supplementary paternity testing

International Congress series, 2004-04, Vol.1261, p.12-14

2004

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Discovery of novel drug sensitivities in T-PLL by high-throughput ex vivo drug testing and mutation profiling

Leukemia, 2018-03, Vol.32 (3), p.774-787

2018

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Discovery of somatic STAT5b mutations in large granular lymphocytic leukemia

Blood, 2013-05, Vol.121 (22), p.4541-4550

2013

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Discovery of STAT5b Mutations and Small Subclones of STAT3 Mutations in Large Granular Lymphocytic (LGL) Leukemia

Blood, 2012-11, Vol.120 (21), p.871-871

2012

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Distinct molecular profiles and shared drug vulnerabilities in pancreatic metastases of renal cell carcinoma

Communications biology, 2024-10, Vol.7 (1), p.1355-18, Article 1355

2024

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Epidemiological and treatment-related factors contribute to improved outcome of oropharyngeal squamous cell carcinoma in Finland

Acta oncologica, 2018-01, Vol.57 (4), p.541-551

2018

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Evaluating Whole Genome Amplification via Multiply-Primed Rolling Circle Amplification for SNP Genotyping of Samples With Low DNA Yield

Twin research and human genetics, 2005-08, Vol.8 (4), p.368-375

2005

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Examining the effect of mitochondrial DNA variants on blood pressure in two Finnish cohorts

Scientific reports, 2021-01, Vol.11 (1), p.611-611, Article 611

2021

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Gender differences in genetic risk profiles for cardiovascular disease

PloS one, 2008-10, Vol.3 (10), p.e3615

2008

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Gender-Specific Associations Between Saliva Microbiota and Body Size

Frontiers in microbiology, 2019, Vol.10, p.767

2019

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242: Profiling Multigenetic Variation in Androgen Pathway as a Risk Factor for Prostate Cancer

251P Characteristics and overall survival of an advanced breast cancer cohort in Finland

825 Exome Sequencing of T-LGL Leukemia Patient Revealed ANGPT2 as a Possible Mutational Target

A6.02 Somatic mutations in clonally expanded CD8+ T cells in patients with newly diagnosed rheumatoid arthritis

Abstract 606: Novel somatic mutations in the DNA-binding and coiled-coil domain of the STAT3 gene in LGL-leukemia

Acquired Somatic Mutations in T Cells in Patients with Aplastic Anemia and Hypoplastic Myelodysplastic Syndromes

Activating somatic mutations outside the SH2-domain of STAT3 in LGL leukemia

ALWAYS THE LITTLE BROTHER? DIGITAL-PRODUCT INNOVATION IN THE MEDIA SECTOR

The analysis of clonal diversity and therapy responses using STAT3 mutations as a molecular marker in large granular lymphocytic leukemia

Analysis of four neuroligin genes as candidates for autism

Association of a Nonsynonymous Variant of DAOA with Visuospatial Ability in a Bipolar Family Sample

Case studies investigating genetic heterogeneity between anatomically distinct bone marrow compartments in acute myeloid leukemia

Chromosome 1 loci in finnish schizophrenia families

Copy number alterations and neoplasia-specific mutations in MELK, PDCD1LG2, TLN1, and PAX5 at 9p in different neoplasias

The CRCbiome study: a large prospective cohort study examining the role of lifestyle and the gut microbiome in colorectal cancer screening participants

Development of SNP microarray for supplementary paternity testing

Discovery of novel drug sensitivities in T-PLL by high-throughput ex vivo drug testing and mutation profiling

Discovery of somatic STAT5b mutations in large granular lymphocytic leukemia

Discovery of STAT5b Mutations and Small Subclones of STAT3 Mutations in Large Granular Lymphocytic (LGL) Leukemia

Distinct molecular profiles and shared drug vulnerabilities in pancreatic metastases of renal cell carcinoma

Epidemiological and treatment-related factors contribute to improved outcome of oropharyngeal squamous cell carcinoma in Finland

Evaluating Whole Genome Amplification via Multiply-Primed Rolling Circle Amplification for SNP Genotyping of Samples With Low DNA Yield

Examining the effect of mitochondrial DNA variants on blood pressure in two Finnish cohorts

Gender differences in genetic risk profiles for cardiovascular disease

Gender-Specific Associations Between Saliva Microbiota and Body Size

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