Author details

Full Name

Priit Palta

Affiliation

ORCID

Career Start Year

2007

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36929174	GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer.	Hum Mol Genet	2023
37633957	Targeted gene expression profiling for accurate endometrial receptivity testing.		2023
36653562	FinnGen provides genetic insights from a well-phenotyped isolated population.	Nature	2023
36829046	Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.	Nature	2023
36653343	Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.	Nat Commun	2023
37079300	Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration.	JAMA Ophthalmol	2023
37453564	Genome-Wide Association Study Identifies 4 Novel Risk Loci for Small Intestinal Neuroendocrine Tumors Including a Missense Mutation in LGR5.	Gastroenterology	2023
34927275	Primary age-related tauopathy in a Finnish population-based study of the oldest old (Vantaa 85+).	Neuropathology and Applied Neurobiology	2022
35978133	Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis.	Commun Biol	2022
34928946	Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples.	PLoS Comput Biol	2021
33249422	High-resolution population-specific recombination rates and their effect on phasing and genotype imputation.	European Journal of Human Genetics	2021
33243845	Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health.	European Respiratory Journal	2021
32154731	Polygenic Hyperlipidemias and Coronary Artery Disease Risk.	Circ Genom Precis Med	2020
31004479	A molecular tool for menstrual cycle phase dating of endometrial samples in endometriosis transcriptome studiesâ¿ .	Biology of Reproduction	2019
31691324		Prenatal Diagnosis	2019
31687746	A molecular tool for menstrual cycle phase dating of endometrial samples in endometriosis transcriptome studiesâ¿ .	Biology of Reproduction	2019
31283802	Computational framework for targeted high-coverage sequencing based NIPT.	PLoS ONE	2019
28103696	Epigenetic DNA methylation changes associated with headache chronification: A retrospective case-control study.	Cephalalgia	2018
29930110	Analysis of shared heritability in common disorders of the brain.	Science	2018
30588329	TAC-seq: targeted DNA and RNA sequencing for precise biomarker molecule counting.	NPJ Genom Med	2018
30420737	Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa.	Mol Psychiatry	2018
30189203	Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.	Neuron	2018
29618827	NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidies.	Scientific Reports	2018
29155802	Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa.	Mol Psychiatry	2018
29731251	Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.	Neuron	2018
28145424	Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom.	Eur J Hum Genet	2017
28643794	Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations.	Nat Commun	2017
28401899	Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel.	Eur J Hum Genet	2017
28031487	Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms.	Proc Natl Acad Sci U S A	2017
27681292	Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.	Nat Genet	2016
27322543	Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.	Nat Genet	2016
26196440	Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.	Transl Psychiatry	2015
25853576	Haplotype phasing and inheritance of copy number variants in nuclear families.	PLoS ONE	2015
27066539	Genetic analysis for a shared biological basis between migraine and coronary artery disease.	Neurol Genet	2015
25078778	Distribution and medical impact of loss-of-function variants in the Finnish founder population.	PLoS Genet	2014
24463507	De novo mutations in schizophrenia implicate synaptic networks.	Nature	2014
24827138	Structural genomic variation as risk factor for idiopathic recurrent miscarriage.	Human Mutation	2014
23793025	Genome-wide meta-analysis identifies new susceptibility loci for migraine.	Nat Genet	2013
24159175	Genome-wide methylation analyses of primary human leukocyte subsets identifies functionally important cell-type-specific hypomethylated regions.	Blood	2013
23209683	A comparison of the whole genome approach of MeDIP-seq to the targeted approach of the Infinium HumanMethylation450 BeadChip(Â®) for methylome profiling.	PLoS One	2012
22473391	No evidence of somatic DNA copy number alterations in eutopic and ectopic endometrial tissue in endometriosis.	Human Reproduction	2012
21356118	Detection of NASBA amplified bacterial tmRNA molecules on SLICSel designed microarray probes.	BMC Biotechnology	2011
21112420	A parallel SNP array study of genomic aberrations associated with mental retardation in patients and general population in Estonia.	European Journal of Medical Genetics	2011
21364695	The GENCODE exome: sequencing the complete human exome.	Eur J Hum Genet	2011
19932073	Comparison of DNA extraction methods for multiplex polymerase chain reaction.	Analytical Biochemistry	2010
20130649	A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.	Nature	2010
20426847	Detection of tmRNA molecules on microarrays at low temperatures using helper oligonucleotides.	BMC Biotechnology	2010
19948333	Evaluation of the 124-plex SNP typing microarray for forensic testing.		2009
19445684	Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications.	BMC Biotechnology	2009
18451793	Array-MAPH: a methodology for the detection of locus copy-number changes in complex genomes.		2008