Lista de obras - Mari Anneli Kaunisto - Dominio Público Uruguay

A high-density association screen of 155 ion transport genes for involvement with common migraine

artículo científico publicado en 2008

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

artículo científico publicado en 2004

A novel splice mutation in PLS3 causes X-linked early onset low-turnover osteoporosis

artículo científico publicado en 2015

A susceptibility locus for migraine with aura, on chromosome 4q24.

scientific article published on 08 February 2002

A visual migraine aura locus maps to 9q21-q22

artículo científico publicado en 2010

Acetazolamide improves neurotological abnormalities in a family with episodic ataxia type 2 (EA-2).

artículo científico publicado en 2004

Analgesic Plasma Concentrations of Oxycodone After Surgery for Breast Cancer-Which Factors Matter?

artículo científico publicado en 2017

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Association analysis of podocyte slit diaphragm genes as candidates for diabetic nephropathy

article

Association of the SLC22A1, SLC22A2, and SLC22A3 genes encoding organic cation transporters with diabetic nephropathy and hypertension

artículo científico publicado en 2010

CACNG2 polymorphisms associate with chronic pain following mastectomy

artículo científico publicado en 2019

CRY1 and CRY2 genetic variants in seasonality: A longitudinal and cross-sectional study

artículo científico publicado en 2016

CRY1, CRY2 and PRKCDBP genetic variants in metabolic syndrome

artículo científico publicado en 2014

CRY2 genetic variants associate with dysthymia

artículo científico publicado en 2013

Chromosome 19p13 loci in Finnish migraine with aura families

artículo científico publicado en 2005

Common Inflammation-Related Candidate Gene Variants and Acute Kidney Injury in 2647 Critically Ill Finnish Patients

article

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

article by Padhraig Gormley et al published 16 May 2018 in Neuron

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

article by Padhraig Gormley et al published September 2018 in Neuron

Consistently replicating locus linked to migraine on 10q22-q23

artículo científico publicado en 2008

Decreased cerebellar total creatine in episodic ataxia type 2: a 1H MRS study.

artículo científico publicado en 2005

Development of an AmpliSeq Panel for Next-Generation Sequencing of a Set of Genetic Predictors of Persisting Pain

article

Effect of catechol-o-methyltransferase-gene (COMT) variants on experimental and acute postoperative pain in 1,000 women undergoing surgery for breast cancer

artículo científico publicado en 2013

Effect of endocannabinoid degradation on pain: role of FAAH polymorphisms in experimental and postoperative pain in women treated for breast cancer

artículo científico publicado en 2016

Elevated MBL concentrations are not an indication of association between the MBL2 gene and type 1 diabetes or diabetic nephropathy

scientific article published on 14 April 2009

Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

artículo científico publicado en 2016

Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort

artículo científico publicado en 2009

Genetic association study of endothelin-1 and its receptors EDNRA and EDNRB in migraine with aura

artículo científico publicado en 2009

Genetic predisposition to acute kidney injury--a systematic review

artículo científico publicado en 2015

Genetic variants in SERPINA4 and SERPINA5, but not BCL2 and SIK3 are associated with acute kidney injury in critically ill patients with septic shock

artículo científico publicado en 2017

Genetic variation in P2RX7 and pain tolerance

artículo científico publicado en 2018

Genetics and genomics in postoperative pain and analgesia

article

Genome-wide association analysis identifies susceptibility loci for migraine without aura

artículo científico publicado en 2012

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

artículo científico publicado en 2010

Genome-wide meta-analysis identifies new susceptibility loci for migraine

artículo científico publicado en 2013

Heme Oxygenase 1 Polymorphisms and Plasma Concentrations in Critically Ill Patients

Heme oxygenase-1 repeat polymorphism in septic acute kidney injury

scientific article published on 23 May 2019

High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms

artículo científico publicado en 2014

How much oxycodone is needed for adequate analgesia after breast cancer surgery: effect of the OPRM1 118A>G polymorphism

artículo científico publicado en 2014

Ischemic stroke is associated with the ABO locus: the EuroCLOT study

artículo científico publicado en 2013

Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2

artículo científico publicado en 2004

Machine-learned analysis of global and glial/opioid intersection-related DNA methylation in patients with persistent pain after breast cancer surgery

scientific article published on 27 November 2019

Machine-learned analysis of the association of next-generation sequencing-based genotypes with persistent pain after breast cancer surgery

artículo científico publicado en 2019

Massive withdrawal symptoms and affective vulnerability are associated with variants of the CHRNA4 gene in a subgroup of smokers

artículo científico publicado en 2014

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

artículo científico publicado en 2016

Migraine without aura: genome-wide association analysis identifies several novel susceptibility.

artículo científico publicado en 2013

Migraine without aura: genome-wide association analysis identifies several novel susceptibility. ⬇️

artículo científico publicado en 2013

Migraine: a complex genetic disorder

artículo científico publicado en 2007

No Association between Genetic Loci near IRF2 and TBX1 and Acute Kidney Injury in the Critically Ill

artículo científico publicado en 2020

No association of migraine to the GABA-A receptor complex on chromosome 15

scientific article published on 01 January 2008

Novel splice site CACNA1A mutation causing episodic ataxia type 2.

artículo científico publicado en 2003

Novel susceptibility locus at 22q11 for diabetic nephropathy in type 1 diabetes

artículo científico publicado en 2011

PRKCDBP (CAVIN3) and CRY2 associate with major depressive disorder

artículo científico publicado en 2016

Pain in 1,000 women treated for breast cancer: a prospective study of pain sensitivity and postoperative pain

artículo científico publicado en 2013

Subclinical vestibulocerebellar dysfunction in migraine with and without aura

artículo científico publicado en 2003

Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set.

artículo científico publicado en 2015

Testing of Variants of the MTHFR and ESR1 Genes in 1798 Finnish Individuals Fails to Confirm the Association with Migraine with Aura

article

The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families

article by Marjo Eveliina Hiekkala et al published 27 February 2018 in Cephalalgia

The molecular genetics of migraine

artículo científico publicado en 2004

Trait components provide tools to dissect the genetic susceptibility of migraine

artículo científico publicado en 2006

Lista de obras de Mari Anneli Kaunisto

A high-density association screen of 155 ion transport genes for involvement with common migraine

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

A novel splice mutation in PLS3 causes X-linked early onset low-turnover osteoporosis

A susceptibility locus for migraine with aura, on chromosome 4q24.

A visual migraine aura locus maps to 9q21-q22

Acetazolamide improves neurotological abnormalities in a family with episodic ataxia type 2 (EA-2).

Analgesic Plasma Concentrations of Oxycodone After Surgery for Breast Cancer-Which Factors Matter?

Analysis of shared heritability in common disorders of the brain

Association analysis of podocyte slit diaphragm genes as candidates for diabetic nephropathy

Association of the SLC22A1, SLC22A2, and SLC22A3 genes encoding organic cation transporters with diabetic nephropathy and hypertension

CACNG2 polymorphisms associate with chronic pain following mastectomy

CRY1 and CRY2 genetic variants in seasonality: A longitudinal and cross-sectional study

CRY1, CRY2 and PRKCDBP genetic variants in metabolic syndrome

CRY2 genetic variants associate with dysthymia

Chromosome 19p13 loci in Finnish migraine with aura families

Common Inflammation-Related Candidate Gene Variants and Acute Kidney Injury in 2647 Critically Ill Finnish Patients

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

Consistently replicating locus linked to migraine on 10q22-q23

Decreased cerebellar total creatine in episodic ataxia type 2: a 1H MRS study.

Development of an AmpliSeq Panel for Next-Generation Sequencing of a Set of Genetic Predictors of Persisting Pain

Effect of catechol-o-methyltransferase-gene (COMT) variants on experimental and acute postoperative pain in 1,000 women undergoing surgery for breast cancer

Effect of endocannabinoid degradation on pain: role of FAAH polymorphisms in experimental and postoperative pain in women treated for breast cancer

Elevated MBL concentrations are not an indication of association between the MBL2 gene and type 1 diabetes or diabetic nephropathy

Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort

Genetic association study of endothelin-1 and its receptors EDNRA and EDNRB in migraine with aura

Genetic predisposition to acute kidney injury--a systematic review

Genetic variants in SERPINA4 and SERPINA5, but not BCL2 and SIK3 are associated with acute kidney injury in critically ill patients with septic shock

Genetic variation in P2RX7 and pain tolerance

Genetics and genomics in postoperative pain and analgesia

Genome-wide association analysis identifies susceptibility loci for migraine without aura

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

Genome-wide meta-analysis identifies new susceptibility loci for migraine

Heme Oxygenase 1 Polymorphisms and Plasma Concentrations in Critically Ill Patients

Heme oxygenase-1 repeat polymorphism in septic acute kidney injury

High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms

How much oxycodone is needed for adequate analgesia after breast cancer surgery: effect of the OPRM1 118A>G polymorphism

Ischemic stroke is associated with the ABO locus: the EuroCLOT study

Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2

Machine-learned analysis of global and glial/opioid intersection-related DNA methylation in patients with persistent pain after breast cancer surgery

Machine-learned analysis of the association of next-generation sequencing-based genotypes with persistent pain after breast cancer surgery

Massive withdrawal symptoms and affective vulnerability are associated with variants of the CHRNA4 gene in a subgroup of smokers

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

Migraine without aura: genome-wide association analysis identifies several novel susceptibility.

Migraine without aura: genome-wide association analysis identifies several novel susceptibility. ⬇️

Migraine: a complex genetic disorder

No Association between Genetic Loci near IRF2 and TBX1 and Acute Kidney Injury in the Critically Ill

No association of migraine to the GABA-A receptor complex on chromosome 15

Novel splice site CACNA1A mutation causing episodic ataxia type 2.

Novel susceptibility locus at 22q11 for diabetic nephropathy in type 1 diabetes

PRKCDBP (CAVIN3) and CRY2 associate with major depressive disorder

Pain in 1,000 women treated for breast cancer: a prospective study of pain sensitivity and postoperative pain

Subclinical vestibulocerebellar dysfunction in migraine with and without aura

Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set.

Testing of Variants of the MTHFR and ESR1 Genes in 1798 Finnish Individuals Fails to Confirm the Association with Migraine with Aura

The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families

The molecular genetics of migraine

Trait components provide tools to dissect the genetic susceptibility of migraine