about
Comparative genome-scale reconstruction of gapless metabolic networks for present and ancestral speciesIntegrated data analysis reveals uterine leiomyoma subtypes with distinct driver pathways and biomarkers.Towards structured output prediction of enzyme functionInferring branching pathways in genome-scale metabolic networksWhole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera.Multiple clinical characteristics separate MED12-mutation-positive and -negative uterine leiomyomas.The Glanville fritillary genome retains an ancient karyotype and reveals selective chromosomal fusions in LepidopteraIdentification of 33 candidate oncogenes by screening for base-specific mutations.Eleven candidate susceptibility genes for common familial colorectal cancerMED12 mutations and FH inactivation are mutually exclusive in uterine leiomyomas.Frequent L1 retrotranspositions originating from TTC28 in colorectal cancer.Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer.Whole-Genome Sequencing of Growth Hormone (GH)-Secreting Pituitary Adenomas.CTCF/cohesin-binding sites are frequently mutated in cancer.Whole-genome metabolic model of Trichoderma reesei built by comparative reconstructionMED12 mutation frequency in unselected sporadic uterine leiomyomas.Detection of subclonal L1 transductions in colorectal cancer by long-distance inverse-PCR and Nanopore sequencing.Global metabolomic profiling of uterine leiomyomas.3'-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivity.Characterization of uterine leiomyomas by whole-genome sequencing.Impact of AIP and inhibitory G protein alpha 2 proteins on clinical features of sporadic GH-secreting pituitary adenomas.Somatic MED12 Nonsense Mutation Escapes mRNA Decay and Reveals a Motif Required for Nuclear Entry.Exome-wide somatic mutation characterization of small bowel adenocarcinoma.Clonally related uterine leiomyomas are common and display branched tumor evolution.Towards pan-genome read alignment to improve variation calling.Discovery of potential causative mutations in human coding and noncoding genome with the interactive software BasePlayerContribution of allelic imbalance to colorectal cancerComprehensive evaluation of coding region point mutations in microsatellite‐unstable colorectal cancerExome sequencing reveals frequent inactivating mutations in ARID1A, ARID1B, ARID2 and ARID4A in microsatellite unstable colorectal cancerGermline alterations in a consecutive series of acute myeloid leukemiaExome and immune cell score analyses reveal great variation within synchronous primary colorectal cancersERCC6L2 defines a novel entity within inherited acute myeloid leukemia
P50
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-9818-6370
@en
name
Esa Pitkänen
@ast
Esa Pitkänen
@en
Esa Pitkänen
@nl
type
label
Esa Pitkänen
@ast
Esa Pitkänen
@en
Esa Pitkänen
@nl
prefLabel
Esa Pitkänen
@ast
Esa Pitkänen
@en
Esa Pitkänen
@nl
P106
P31
P496
0000-0002-9818-6370