List of works - Pasi A. Koivisto

Absence of KLF6 gene mutations in human astrocytic tumors and cell lines.

scientific article published in September 2004

Amplification and overexpression of vinculin are associated with increased tumour cell proliferation and progression in advanced prostate cancer

scientific article published on 5 January 2011

Androgen Receptor Gene Alterations in Finnish Male Breast Cancer

article

Androgen receptor CAG polymorphism and prostate cancer risk

scholarly article by Nina Mononen et al published 3 July 2002 in Human Genetics

Androgen receptor amplification is associated with increased cell proliferation in prostate cancer

scientific article published on 10 January 2007

Androgen receptor mutations in high-grade prostate cancer before hormonal therapy.

scientific article

BRCA2 mutations in 154 finnish male breast cancer patients

scientific article

Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors

scientific article

Clinical validation of candidate genes associated with prostate cancer progression in the CWR22 model system using tissue microarrays

article

Defining the region(s) of deletion at 6q16-q22 in human prostate cancer

scientific article

Deletion, mutation, and loss of expression of KLF6 in human prostate cancer

scientific article

Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene

scientific article

Expression patterns of potential therapeutic targets in prostate cancer.

scientific article published in February 2005

FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation

scientific article

GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

scientific article published on May 2009

Genetic changes in familial prostate cancer by comparative genomic hybridization

scientific article published on 01 February 2001

Genome-wide scan for linkage in finnish hereditary prostate cancer (HPC) families identifies novel susceptibility loci at 11q14 and 3p25-26.

scientific article

Germline alterations of the RNASEL gene, a candidate HPC1 gene at 1q25, in patients and families with prostate cancer

scientific article published on 8 April 2002

Germline mutation analysis of the androgen receptor gene in Finnish patients with prostate cancer.

scientific article

Hemochromatosis gene mutations among Finnish male breast and prostate cancer patients

scientific article published on 01 January 2006

Hereditary prostate cancer in Finland: fine-mapping validates 3p26 as a major predisposition locus

scholarly article by Annika R�kman et al published 11 November 2004 in Human Genetics

High NRBP1 expression in prostate cancer is linked with poor clinical outcomes and increased cancer cell growth

scientific article

Incidence of cancer in finnish families with clinically aggressive and nonaggressive prostate cancer

scientific article published on 20 October 2009

Is 5-HTTLPR linked to the response of selective serotonin reuptake inhibitors in MDD?

scientific article published on 17 July 2010

Kruppel-like factor 6 germ-line mutations are infrequent in Finnish hereditary prostate cancer

scientific article published in August 2004

Letter to the editor: Novel GJA1 mutation in oculodentodigital dysplasia

scientific article published on 01 November 2005

MYH9-Related Disease

MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness

scientific article

Pattern of somatic androgen receptor gene mutations in patients with hormone-refractory prostate cancer

scientific article published in November 2002

Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease

scientific article

SERT and NET polymorphisms, temperament and antidepressant response

scientific article

Segregation analysis of 1,546 prostate cancer families in Finland shows recessive inheritance

scientific article

Serotonin transporter (5-HTTLPR) and norepinephrine transporter (NET) gene polymorphisms: susceptibility and treatment response of electroconvulsive therapy in treatment resistant depression

scientific article published in February 2015

Vascular influences of calcium supplementation and vitamin D-induced hypercalcemia in NaCl-hypertensive rats

scientific article published in September 2003

List of works by Pasi A. Koivisto

Absence of KLF6 gene mutations in human astrocytic tumors and cell lines.

Amplification and overexpression of vinculin are associated with increased tumour cell proliferation and progression in advanced prostate cancer

Androgen Receptor Gene Alterations in Finnish Male Breast Cancer

Androgen receptor CAG polymorphism and prostate cancer risk

Androgen receptor amplification is associated with increased cell proliferation in prostate cancer

Androgen receptor mutations in high-grade prostate cancer before hormonal therapy.

BRCA2 mutations in 154 finnish male breast cancer patients

Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors

Clinical validation of candidate genes associated with prostate cancer progression in the CWR22 model system using tissue microarrays

Defining the region(s) of deletion at 6q16-q22 in human prostate cancer

Deletion, mutation, and loss of expression of KLF6 in human prostate cancer

Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene

Expression patterns of potential therapeutic targets in prostate cancer.

FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation

GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

Genetic changes in familial prostate cancer by comparative genomic hybridization

Genome-wide scan for linkage in finnish hereditary prostate cancer (HPC) families identifies novel susceptibility loci at 11q14 and 3p25-26.

Germline alterations of the RNASEL gene, a candidate HPC1 gene at 1q25, in patients and families with prostate cancer

Germline mutation analysis of the androgen receptor gene in Finnish patients with prostate cancer.

Hemochromatosis gene mutations among Finnish male breast and prostate cancer patients

Hereditary prostate cancer in Finland: fine-mapping validates 3p26 as a major predisposition locus

High NRBP1 expression in prostate cancer is linked with poor clinical outcomes and increased cancer cell growth

Incidence of cancer in finnish families with clinically aggressive and nonaggressive prostate cancer

Is 5-HTTLPR linked to the response of selective serotonin reuptake inhibitors in MDD?

Kruppel-like factor 6 germ-line mutations are infrequent in Finnish hereditary prostate cancer

Letter to the editor: Novel GJA1 mutation in oculodentodigital dysplasia

MYH9-Related Disease

MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness

Pattern of somatic androgen receptor gene mutations in patients with hormone-refractory prostate cancer

Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease

SERT and NET polymorphisms, temperament and antidepressant response

Segregation analysis of 1,546 prostate cancer families in Finland shows recessive inheritance

Serotonin transporter (5-HTTLPR) and norepinephrine transporter (NET) gene polymorphisms: susceptibility and treatment response of electroconvulsive therapy in treatment resistant depression

Vascular influences of calcium supplementation and vitamin D-induced hypercalcemia in NaCl-hypertensive rats