Lista de obras - Kimmo Palin - Dominio Público Uruguay

Association analyses identify 31 new risk loci for colorectal cancer susceptibility

artículo científico publicado en 2019

Bayesian refinement of association signals for 14 loci in 3 common diseases

artículo científico publicado en 2012

CTCF/cohesin-binding sites are frequently mutated in cancer

artículo científico publicado en 2015

Clinical characterization, genetic mapping and whole-genome sequence analysis of a novel autosomal recessive intellectual disability syndrome

artículo científico publicado en 2014

Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

artículo científico publicado en 2017

Contribution of allelic imbalance to colorectal cancer

scientific article published in Nature Communications

Correlating gene promoters and expression in gene disruption experiments

artículo científico publicado en 2002

DNA-binding specificities of human transcription factors

scientific journal article

Detection of subclonal L1 transductions in colorectal cancer by long-distance inverse-PCR and Nanopore sequencing

artículo científico publicado en 2017

Exome and immune cell score analyses reveal great variation within synchronous primary colorectal cancers

scientific article published on 21 March 2019

Exome-wide somatic mutation characterization of small bowel adenocarcinoma.

artículo científico publicado en 2018

Fast motif matching revisited: high-order PWMs, SNPs and indels

artículo científico publicado en 2016

Frequent L1 retrotranspositions originating from TTC28 in colorectal cancer.

artículo científico publicado en 2014

From gene networks to gene function

artículo científico publicado en 2003

Genetic predisposition to uterine leiomyoma is determined by loci for genitourinary development and genome stability

article

Genome-wide analysis of ETS-family DNA-binding in vitro and in vivo

artículo científico publicado en 2010

Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci

artículo científico publicado en 2017

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

artículo científico publicado en 2010

Genome-wide prediction of mammalian enhancers based on analysis of transcription-factor binding affinity

artículo científico publicado en 2006

Human cell transformation by combined lineage conversion and oncogene expression

artículo científico publicado en 2021

Identification of candidate oncogenes in human colorectal cancers with microsatellite instability

artículo científico publicado en 2013

Identity-by-descent-based phasing and imputation in founder populations using graphical models

artículo científico publicado en 2011

Integrating sequence, evolution and functional genomics in regulatory genomics

artículo científico publicado en 2009

Locating potential enhancer elements by comparative genomics using the EEL software

scholarly article by Kimmo Palin et al published June 2006 in Nature Protocols

Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer

artículo científico publicado en 2016

Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer

artículo científico publicado en 2017

Multiple clinical characteristics separate MED12-mutation-positive and -negative uterine leiomyomas.

artículo científico publicado en 2017

Multiplexed massively parallel SELEX for characterization of human transcription factor binding specificities

artículo científico publicado en 2010

Parity associates with chromosomal damage in uterine leiomyomas

artículo científico publicado en 2021

Pro-inflammatory fatty acid profile and colorectal cancer risk: A Mendelian randomisation analysis

artículo científico publicado en 2017

Retrotransposon insertions can initiate colorectal cancer and are associated with poor survival

artículo científico publicado en 2019

Systematic search for rare variants in Finnish early-onset colorectal cancer patients

artículo científico publicado en 2014

The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling.

artículo científico publicado en 2009

Uterine leiomyoma-linked MED12 mutations disrupt mediator-associated CDK activity.

artículo científico publicado en 2014

Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease

artículo científico publicado en 2016

Lista de obras de Kimmo Palin

Association analyses identify 31 new risk loci for colorectal cancer susceptibility

Bayesian refinement of association signals for 14 loci in 3 common diseases

CTCF/cohesin-binding sites are frequently mutated in cancer

Clinical characterization, genetic mapping and whole-genome sequence analysis of a novel autosomal recessive intellectual disability syndrome

Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

Contribution of allelic imbalance to colorectal cancer

Correlating gene promoters and expression in gene disruption experiments

DNA-binding specificities of human transcription factors

Detection of subclonal L1 transductions in colorectal cancer by long-distance inverse-PCR and Nanopore sequencing

Exome and immune cell score analyses reveal great variation within synchronous primary colorectal cancers

Exome-wide somatic mutation characterization of small bowel adenocarcinoma.

Fast motif matching revisited: high-order PWMs, SNPs and indels

Frequent L1 retrotranspositions originating from TTC28 in colorectal cancer.

From gene networks to gene function

Genetic predisposition to uterine leiomyoma is determined by loci for genitourinary development and genome stability

Genome-wide analysis of ETS-family DNA-binding in vitro and in vivo

Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Genome-wide prediction of mammalian enhancers based on analysis of transcription-factor binding affinity

Human cell transformation by combined lineage conversion and oncogene expression

Identification of candidate oncogenes in human colorectal cancers with microsatellite instability

Identity-by-descent-based phasing and imputation in founder populations using graphical models

Integrating sequence, evolution and functional genomics in regulatory genomics

Locating potential enhancer elements by comparative genomics using the EEL software

Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer

Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer

Multiple clinical characteristics separate MED12-mutation-positive and -negative uterine leiomyomas.

Multiplexed massively parallel SELEX for characterization of human transcription factor binding specificities

Parity associates with chromosomal damage in uterine leiomyomas

Pro-inflammatory fatty acid profile and colorectal cancer risk: A Mendelian randomisation analysis

Retrotransposon insertions can initiate colorectal cancer and are associated with poor survival

Systematic search for rare variants in Finnish early-onset colorectal cancer patients

The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling.

Uterine leiomyoma-linked MED12 mutations disrupt mediator-associated CDK activity.

Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease