Author details

Full Name

Helena Kilpinen

Affiliation

ORCID

Career Start Year

2007

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36684426	Differentiation of human induced pluripotent stem cells into cortical neural stem cells.	Front Cell Dev Biol	2023
37082143	Somatic mutations alter the differentiation outcomes of iPSC-derived neurons.		2023
36697831	Author Correction: Genomic basis for RNA alterations in cancer.	Nature	2023
35063129	CRISPR activation enables high-fidelity reprogramming into human pluripotent stem cells.	Stem Cell Reports	2022
32773033	Population-scale proteome variation in human induced pluripotent stem cells.	Elife	2020
31160811	Publisher Correction: Molecular and functional variation in iPSC-derived sensory neurons.	Nat Genet	2019
29229984	Molecular and functional variation in iPSC-derived sensory neurons.	Nat Genet	2018
28614302	Corrigendum: Common genetic variation drives molecular heterogeneity in human iPSCs.	Nature	2017
28489815	Common genetic variation drives molecular heterogeneity in human iPSCs.	Nature	2017
26300124	Population Variation and Genetic Control of Modular Chromatin Architecture in Humans.	Cell	2015
26440885	Mondo-Mlx Mediates Organismal Sugar Sensing through the Gli-Similar Transcription Factor Sugarbabe.	Cell Reports	2015
23164818	Common variant at 16p11.2 conferring risk of psychosis.	Mol Psychiatry	2014
25363760	Synaptic, transcriptional and chromatin genes disrupted in autism.	Nature	2014
24169524	Allele-specific regulation of DISC1 expression by miR-135b-5p.	European Journal of Human Genetics	2014
24255646	Identification and removal of low-complexity sites in allele-specific analysis of ChIP-seq data.	Bioinformatics	2014
23103023	How next-generation sequencing is transforming complex disease genetics.	Trends in Genetics	2013
24037378	Transcriptome and genome sequencing uncovers functional variation in humans.	Nature	2013
24136355	Coordinated effects of sequence variation on DNA binding, chromatin structure, and transcription.	Science	2013
22976472	Genetic and epigenetic contribution to complex traits.	Hum Mol Genet	2012
19454485	Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland.	Human Molecular Genetics	2009
17579608	Association of DISC1 with autism and Asperger syndrome.	Molecular Psychiatry	2008
19360665	Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism.	Autism Research	2008
17185386	Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.	Human Molecular Genetics	2007
17673452	Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments.	Human Molecular Genetics	2007