Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

A. Palotie · SciRah

Researcher profile · Semantic Scholar

A. Palotie

Share profile

A. Palotie — researcher profile on SciRah

h-index: 143
Works: 930
Citations: 122K

Most-cited papers

Translational genomics of osteoarthritis in 1,962,069 individuals
K. Hatzikotoulas, L. Southam, L. Stefánsdóttir, C. Boer +169 more
2025Nature95 citations Open access
Semantic Scholar
Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes
A. Elliott, R. Walters, M. Pirinen, M. Kurki +23 more
2024Nature Genetics88 citations Open access
Semantic Scholar
Cardiovascular Significance and Genetics of Epicardial and Pericardial Adiposity.
Joel T. Rämö, S. Kany, C. Hou, S. Friedman +8 more
2024JAMA cardiology47 citations Open access
Semantic Scholar
Genetic drivers and cellular selection of female mosaic X chromosome loss
Ao-Xing Liu, G. Genovese, Ya-Jie Zhao, M. Pirinen +41 more
2024Nature45 citations Open access
Semantic Scholar
Understanding the genetic complexity of puberty timing across the allele frequency spectrum
K. Kentistou, L. R. Kaisinger, S. Stankovic, Marc Vaudel +217 more
2024Nature Genetics40 citations Open access
Semantic Scholar
High Burden of Ileus and Pneumonia in Clozapine-Treated Individuals With Schizophrenia: A Finnish 25-Year Follow-Up Register Study.
Juulia J. Partanen, P. Häppölä, A. Kämpe, Ari V. Ahola-Olli +13 more
2024American Journal of Psychiatry38 citations Open access
Semantic Scholar
The impact of common and rare genetic variants on bradyarrhythmia development
Lu-Chen Weng, Joel T. Rämö, S. Jurgens, S. Khurshid +103 more
2025Nature Genetics20 citations Open access
Semantic Scholar
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events
H. Heyne, Fanny-Dhelia Pajuste, J. Wanner, Jennifer I. Daniel Onwuchekwa +4 more
2024Nature Communications20 citations Open access
Semantic Scholar
Thrombosis Risk in Double Heterozygous Carriers of Factor V Leiden and Prothrombin G20210A in FinnGen and the UK Biobank.
Justine Ryu, Joel T. Rämö, S. Jurgens, T. Niiranen +8 more
2024Blood20 citations Open access
Semantic Scholar
Association of early blood-based biomarkers and six-month functional outcomes in conventional severity categories of traumatic brain injury: capturing the continuous spectrum of injury
L. Wilson, V. Newcombe, D. Whitehouse, S. Mondello +250 more
2024EBioMedicine19 citations Open access
Semantic Scholar
Polygenic liability for antipsychotic dosage and polypharmacy - a real-world registry and biobank study
E. Koch, A. Kämpe, M. Alver, Sindri Sigurðarson +17 more
2024Neuropsychopharmacology15 citations Open access
Semantic Scholar
Monoallelic TYROBP deletion is a novel risk factor for Alzheimer’s disease
H. Martiskainen, R. Willman, P. Harju, S. Heikkinen +353 more
2025Molecular Neurodegeneration13 citations Open access
Semantic Scholar
Risk Variants Associated With Normal Pressure Hydrocephalus
Joel Räsänen, S. Heikkinen, Kiira Mäklin, A. Lipponen +30 more
2024Neurology13 citations Open access
Semantic Scholar
Population-scale multiome immune cell atlas reveals complex disease drivers
M. Kanai, T. Delorey, J. Honkanen, R. Rodosthenous +33 more
2025medRxiv12 citations Open access
Semantic Scholar
Beyond mild, moderate, and severe traumatic brain injury: modelling severity from clinical, neuroimaging, and blood-based indicators
Lindsay D. Nelson, Brooke E. Magnus, John K. Yue, Steve Balsis +268 more
2025EBioMedicine12 citations Open access
Semantic Scholar
Cross‐sectional study of plasma phosphorylated tau 217 in persons without dementia
T. Saari, T. Palviainen, M. Hiltunen, S. Herukka +10 more
2024medRxiv12 citations Open access
Semantic Scholar
A cross-disorder analysis of CNVs finds novel loci and dose-dependent relationships of genes to psychiatric traits
O. Shanta, M. Klein, Molly Sacks, J. MacDonald +235 more
2025medRxiv11 citations Open access
Semantic Scholar
Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma
Joel T. Rämö, B. Gorman, Lu-Chen Weng, S. Jurgens +27 more
2025Nature Communications11 citations Open access
Semantic Scholar
Genomic analyses implicate hormonal and metabolic dysregulation in polycystic ovary syndrome
L. Moolhuijsen, Jia Zhu, B. Mullin, N. Pujol-Gualdo +91 more
2026Nature Genetics10 citations Open access
Semantic Scholar
Genetic Analysis of Obstructive Sleep Apnea and Its Relationship with Severe COVID-19
S. Strausz, E. Agafonova, Varvara Tiullinen, T. Kiiskinen +10 more
2024Annals of the American Thoracic Society10 citations Open access
Semantic Scholar
Genetic contribution to disease-course severity and progression in the SUPER-Finland study, a cohort of 10,403 individuals with psychotic disorders
A. Kämpe, J. Suvisaari, M. Lähteenvuo, T. Singh +22 more
2024Molecular Psychiatry9 citations Open access
Semantic Scholar
Multitrait analyses identify genetic variants associated with aortic valve function and aortic stenosis risk
S. Kany, Joel T. Rämö, C. Hou, S. Jurgens +12 more
2025Nature Genetics8 citations Open access
Semantic Scholar
Assessing the potential causal effects of 1099 plasma metabolites on 2099 binary disease endpoints
Xian-Yong Yin, Jack Li, D. Bose, Jeffrey Okamoto +19 more
2025Nature Communications8 citations Open access
Semantic Scholar
Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability
L. Urpa, M. Kurki, Elisa J. Rahikkala, E. Hämäläinen +16 more
2024European Journal of Human Genetics8 citations Open access
Semantic Scholar
Genetic and functional analysis of Raynaud’s syndrome implicates loci in vasculature and immunity
A. Tervi, M. Ramste, E. Abner, P. Cheng +25 more
2024Cell Genomics8 citations Open access
Semantic Scholar
Psychiatric disorders converge on common pathways but diverge in cellular context, spatial distribution, and directionality of genetic effects
W. Engchuan, O. Shanta, Kuldeep Kumar, J. MacDonald +246 more
2025medRxiv7 citations Open access
Semantic Scholar
Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects
M. Broberg, M. Ampuja, S. Jones, T. Ojala +7 more
2024BMC Genomics7 citations Open access
Semantic Scholar
Genome-wide association analyses of autoimmune hypothyroidism reveal autoimmune and thyroid-specific contributions and an inverse relationship with cancer risk
M. P. Reeve, M. Kanai, Daniel B. Graham, J. Karjalainen +21 more
2026Nature Genetics6 citations Open access
Semantic Scholar
Genetic regulation across germline and somatic variation on the Y chromosome contributes to type 2 diabetes
Go Sato, Yuji Yamamoto, K. Sonehara, R. Saiki +60 more
2026Nature Medicine6 citations Open access
Semantic Scholar
Non-microglial downregulation of PLCG2 impairs synaptic function and elicits Alzheimer disease-related hallmarks
Audrey Coulon, F. Rabiller, M. Takalo, Avishek Roy +62 more
2026bioRxiv5 citations Open access
Semantic Scholar
131 genetic loci highlight immunological pathways and tissues in nasal polyposis and asthma
E. Saarentaus, Kasper Fischer-Rasmussen, E. Sliz, A. Bizaki-Vallaskangas +7 more
2025Nature Communications5 citations Open access
Semantic Scholar
HMG-CoA reductase is a potential therapeutic target for migraine: a mendelian randomization study
Kang Qu, Ming-Xi Li, Peng Yu, A. Palotie +68 more
2024Scientific Reports5 citations Open access
Semantic Scholar
Inherited infertility: Mapping loci associated with impaired female reproduction
S. Ruotsalainen, J. Karjalainen, M. Kurki, E. Lahtela +10 more
2024American Journal of Human Genetics5 citations Open access
Semantic Scholar
Genome-wide association study of borderline personality disorder identifies 11 loci and highlights shared risk with mental and somatic disorders
F. Streit, S. Awasthi, Alisha S. M. Hall, A. Braun +147 more
2024medRxiv5 citations Open access
Semantic Scholar
High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases.
Omar Z. Youssef, A. Loukola, Yossra H. S. Zidi-Mouaffak, Max Tamlander +7 more
2024Laboratory investigation; a journal of technical methods and pathology5 citations Open access
Semantic Scholar
Fine-mapping a genome-wide meta-analysis of 98,374 migraine cases identifies 181 sets of candidate causal variants
Heidi Hautakangas, Joonas Kartau, A. Palotie, Matti Pirinen
2026Nature Communications4 citations Open access
Semantic Scholar
Cross-sectional assessment of telephone- and computer-administered instruments in detection of cognitive impairment
A. Aaltonen, T. Saari, M. Urjansson, T. Palviainen +7 more
2026Journal of Clinical and Experimental Neuropsychology3 citations Open access
Semantic Scholar
Validity of telephone-administered word list learning measures for assessment of episodic memory in aging and Alzheimer's disease.
T. Saari, A. Aaltonen, Karin Lohi, T. Palviainen +7 more
2025Neuropsychology3 citations Open access
Semantic Scholar
Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty
Jonathan K. L. Mak, C. Qin, M. Krüger, Anna Kuukka +323 more
2025Nature Aging3 citations Open access
Semantic Scholar
Genome-wide association study indicates novel associations of annexin A13 to secretory and GAS2L2 with mucous otitis media
A. Bizaki-Vallaskangas, Joel T. Rämö, E. Sliz, I. Kivekäs +10 more
2024Scientific Reports3 citations Open access
Semantic Scholar
Altered neurodevelopmental trajectories of brain structure in Tourette syndrome and Chronic Tic Disorders
Ying Jin, Yu-Xin Guo, Jonathan M. Koller, S. Grossen +79 more
2026medRxiv2 citations Open access
Semantic Scholar
Blood donor biobank pipeline to collect genome-based samples for research
Jarno Honkanen, Veera A. Timonen, J. Koski, J. Juvila +10 more
2025bioRxiv2 citations Open access
Semantic Scholar
Sleep and schizophrenia polygenic scores in non-affective and affective psychotic disorders
Erik Cederlöf, M. Holm, A. Kämpe, Ari V. Ahola-Olli +17 more
2025Psychological Medicine2 citations Open access
Semantic Scholar
Low prevalence of CWH43 variants among Finnish and Norwegian idiopathic normal pressure hydrocephalus patients: a cohort-based observational study
Joel Räsänen, S. Helisalmi, S. Heikkinen, Joose Raivo +29 more
2025Fluids and Barriers of the CNS2 citations Open access
Semantic Scholar
Paediatric traumatic brain injury: clinical presentation, treatment approaches, management strategies, and outcomes. Insights from the CENTER-TBI study
Francesca Graziano, Angelo Guglielmi, Michela Consonni, G. Ogliari +255 more
2025Journal of Anesthesia Analgesia and Critical Care2 citations Open access
Semantic Scholar
Genetic risk for open angle glaucoma subtypes is associated with specific visual field defect classes
S. Sekimitsu, K. Selvan, Yan Zhao, Saber Kazeminasab Hashemabad +11 more
2025Ophthalmology (Rochester, Minn.)2 citations Open access
Semantic Scholar
Regulatory variation at serotonin receptor 1F (HTR1F) modulates arousals and risk for sleep apnea
H. Ollila, S. Strausz, M. Broberg, S. Jones +9 more
2024medRxiv2 citations Open access
Semantic Scholar
High incidence and geographic distribution of cleft palate cases in Finland are associated with a regulatory variant in IRF6
F. Rahimov, P. Nieminen, P. Kumari, E. Juuri +26 more
2024medRxiv2 citations Open access
Semantic Scholar
Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance
H. Mei, Jeannette Simino, Lianna Li, F. Jiang +63 more
2024Alzheimer's Research & Therapy2 citations Open access
Semantic Scholar
Associations of proteomic and epigenetic aging clocks with Alzheimer's disease phenotypes: An exploratory analysis
Cindy David Sarmento, G. Drouard, T. Saari, A. Aaltonen +12 more
2026Alzheimer's & Dementia1 citations Open access
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

S. Ripatti×13
Invite
S. Ripatti — researcher profile on SciRah
M. Kurki×12
Invite
M. Kurki — researcher profile on SciRah
Joel T. Rämö×9
Invite
Joel T. Rämö — researcher profile on SciRah
M. Pirinen×8
Invite
M. Pirinen — researcher profile on SciRah

×8

Invite

T. Esko — researcher profile on SciRah

Invite

V. Julkunen — researcher profile on SciRah

Invite

M. Daly — researcher profile on SciRah

Invite

R. Mägi — researcher profile on SciRah

K. Stefánsson×6

Invite

K. Stefánsson — researcher profile on SciRah

Invite

M. Daly — researcher profile on SciRah

Invite

H. Ollila — researcher profile on SciRah

S. Heikkinen×6

Invite

S. Heikkinen — researcher profile on SciRah