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Priit Palta

Professor of Translational Genomics

University of Tartu

Estonia

Research Interests

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Professors in Biostatistics

About

Priit Palta serves as an Assistant Professor at the University of Helsinki in Finland. His research primarily focuses on genetic studies related to various conditions, including psoriasis, cleft palate, diabetes, and migraine. With a keen interest in the intersection between genetics and socioeconomic factors, he has contributed to several recent articles that explore these themes and their implications. His work supports advancements in understanding complex health issues and their genetic underpinnings.

Articles (29)

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Collaborators (72)

Hanna Ollila

University of Helsinki

FINLAND

Priit Palta

Research Interests

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About

Articles (29)

Genetic variants affect diurnal glucose levels throughout the day

Characterization of genetic loci associated with allergic conjunctivitis

BinDel

Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty

The Estonian Biobank’s journey from biobanking to personalized medicine

Monoallelic TYROBP deletion is a novel risk factor for Alzheimer's disease

Job-related exhaustion risk variant in UST is associated with dementia and DNA methylation

Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes

HMG-CoA reductase is a potential therapeutic target for migraine

Genetic Study of Psoriasis Highlights its Close Link with Socioeconomic Status and Affective Symptoms

Novel loci and biomedical consequences of iron homoeostasis variation

High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene

Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations

Genome-wide association study of anterior uveitis

Genome-wide screen of otosclerosis in population biobanks

FinnGen provides genetic insights from a well-phenotyped isolated population

Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration

Causal relationships between migraine and microstructural white matter

GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer

Migraine, chronic kidney disease and kidney function: observational and genetic analyses.

Genome wide association study identifies 4 novel risk loci for small intestinal neuroendocrine tumors including a missense mutation in LGR5.

A causal effects of gut microbiota in the development of migraine

Targeted gene expression profiling for accurate endometrial receptivity testing

Meta-analysis fine-mapping is often miscalibrated at single-variant resolution

Global Biobank Meta-analysis Initiative

Primary age-related tauopathy in a Finnish population-based study of the oldest old (Vantaa 85+)

Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis

Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples

Association and genetic overlap between clinical chemistry tests and migraine

Collaborators (72)

Hanna Ollila

Joel Rämö

Paula Kauppi

Amy Mason

Andrea Ganna

David Rice

Timo Sipilä

Valeria Lo Faro

Javier Gracia-Tabuenca

Matti Pirinen

Marja-Riitta Taskinen

Juulia Partanen

Auli Karhu

Dirk Paul

Toni Lemmetyinen

Mari Kaunisto

Fatma Doagu

Nomdo M. Jansonius

Ilkka Kalliala

Nina Mars

Tiinamaija Tuomi

Joni Turunen

Lauri Aaltonen

Bertram Kjerulff

Danielle Posthuma

Saara Ollila

Taru Tukiainen

tomi makela

Aarno Palotie

Martti Färkkilä

Hannele Laivuori

Lea Urpa

Juho Wedenoja

Elmo Saarentaus

Reedik Mägi

Reetta Hinttala

Andres Salumets

Alexandra Lahtinen

Aino Salminen

Juhani Määttä

Ying Wang

Karol Bomsztyk

Triin Laisk

Kaur Alasoo