Olli Pietiläinen

Broad Institute — United States

Health Professions · Health Sciences

50h-index25.3kcitations200works5.62yr avg
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Research Topics

Workplace Health and Well-being(59), Genetic Associations and Epidemiology(42), Employment and Welfare Studies(41), Genomics and Rare Diseases(30), Genomic variations and chromosomal abnormalities(29)

Publications172 total

Functional KCC2 expression marks an evolutionarily conserved population of early-maturing interneurons in the perinatal cortex
Nature Communications·2025Open Access
23. RARE CODING VARIANTS IN SCHIZOPHRENIA HAVE ADDITIVE EFFECTS ON POLYGENIC RISK AND ASSOCIATE WITH COGNITIVE ABILITIES IN INDIVIDUALS WITH PSYCHOTIC DISORDERS
European Neuropsychopharmacology·2025Open Access
Control of Golgi- V-ATPase through Sac1-dependent co-regulation of PI(4)P and cholesterol
Nature Communications·2025· 2 citedOpen Access
Polygenic Scores for Schizophrenia and Educational Attainment Predict Global Functioning Across Psychiatric Hospitalization Among People with Schizophrenia
2025Open Access
miRNA profiling of hiPSC-derived neurons from monozygotic twins discordant for schizophrenia
Schizophrenia·2025Open Access
Astrocytic-supplied cholesterol drives synaptic gene expression programs in developing neurons and downstream astrocytic transcriptional programs
2025· 3 citedOpen Access
Control of Golgi- V-ATPase through Sac1-dependent co-regulation of PI(4)P and cholesterol
2024Open Access
6. DECIPHERING NEURONAL NETWORK DEFECTS IN SCHIZOPHRENIA USING MICROFLUIDIC CULTURES
European Neuropsychopharmacology·2024
5. POLYGENIC RISK PREDICTS GLOBAL FUNCTIONING ACROSS INPATIENT PSYCHIATRIC HOSPITALIZATION AMONG PEOPLE WITH SCHIZOPHRENIA
European Neuropsychopharmacology·2024
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
UNC Libraries·2024Open Access
Single-nucleus sequencing reveals enriched expression of genetic risk factors in extratelencephalic neurons sensitive to degeneration in ALS
Nature Aging·2024· 29 citedOpen Access
Genomic, molecular, and cellular divergence of the human brain
Trends in Neurosciences·2024· 12 citedOpen Access
X-chromosome inactivation in human iPSCs provides insight into X-regulated gene expression in autosomes
Genome biology·2024· 14 citedOpen Access
Antipsychotic medications and sleep problems in patients with schizophrenia
Schizophrenia Research·2024· 15 citedOpen Access
Astrocytes Regulate Neuronal Network Burst Frequency Through NMDA Receptors in a Species- and Donor-Specific Manner
Biological Psychiatry Global Open Science·2024· 4 citedOpen Access
Genetic contribution to disease-course severity and progression in the SUPER-Finland study, a cohort of 10,403 individuals with psychotic disorders
Molecular Psychiatry·2024· 9 citedOpen Access
Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability
European Journal of Human Genetics·2024· 6 citedOpen Access
Astrocytes regulate neuronal network burst frequency through NMDA receptors species- and donor-specifically
2023· 2 citedOpen Access
X-chromosome inactivation in human iPSCs provides insight into escape-regulated gene expression
2023· 1 citedOpen Access
W88. PHENOTYPIC AND GENETIC CHARACTERIZATION OF INDIVIDUALS WITH SCHIZOPHRENIA AND HIGH PSYCHIATRIC HOSPITALIZATION BURDEN
European Neuropsychopharmacology·2023
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Frequent Co-authors

Jouko Lönnqvist(16), Tiina Paunio(16), Jaana Suvisaari(15), Srdjan Djurovic(13), David Collier(13), Ossi Rahkonen(13), Dan Rujescu(12), Engilbert Sigurðsson(12), Ina Giegling(12), Ole A. Andreassen(12), Annamari Tuulio‐Henriksson(12), Aarno Palotie(12), Hreinn Stefánsson(11), Sven Cichon(11), Andrés Ingason(11), Thomas Folkmann Hansen(11), Ingrid Melle(11), Marcella Rietschel(11), Hannes Pétursson(11), David St Clair(11)