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M. Kurki · SciRah

Researcher profile · Semantic Scholar

M. Kurki

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M. Kurki — researcher profile on SciRah

h-index: 52
Works: 181
Citations: 28K

Most-cited papers

FinnGen provides genetic insights from a well-phenotyped isolated population
M. Kurki, J. Karjalainen, P. Palta, Timo P. Sipilä +164 more
2023Nature3,914 citations Open access
Semantic Scholar
A cross-population atlas of genetic associations for 220 human phenotypes
S. Sakaue, M. Kanai, Yosuke Tanigawa, J. Karjalainen +42 more
2021Nature Genetics1,992 citations Open access
Semantic Scholar
New insights into the genetic etiology of Alzheimer’s disease and related dementias
C. Bellenguez, F. Küçükali, I. Jansen, L. Kleineidam +496 more
2022Nature Genetics1,984 citations Open access
Semantic Scholar
Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers
N. Mars, J. Koskela, P. Ripatti, T. Kiiskinen +13 more
2020Nature Medicine395 citations Open access
Semantic Scholar
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Wei Zhou, M. Kanai, Kuan-Han H. Wu, Humaira Rasheed +148 more
2022Cell Genomics388 citations Open access
Semantic Scholar
Proteomic aging clock predicts mortality and risk of common age-related diseases in diverse populations
M. Argentieri, Si-Hao Xiao, D. Bennett, Laura M. Winchester +20 more
2023Nature Medicine318 citations Open access
Semantic Scholar
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
T. Als, M. Kurki, J. Grove, G. Voloudakis +39 more
2023Nature Medicine294 citations Open access
Semantic Scholar
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
R. Stevelink, C. Campbell, Si-Wei Chen, B. Abou-Khalil +315 more
2023Nature Genetics198 citations Open access
Semantic Scholar
Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health
S. Strausz, S. Ruotsalainen, H. Ollila, J. Karjalainen +19 more
2020European Respiratory Journal156 citations Open access
Semantic Scholar
Genetic associations of protein-coding variants in human disease
B.-B. Sun, M. Kurki, C. Foley, A. Mechakra +11 more
2021Nature135 citations Open access
Semantic Scholar
GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer
Wei Zhou, B. Brumpton, O. Kabil, J. Gudmundsson +52 more
2020Nature Communications119 citations Open access
Semantic Scholar
Trans-biobank analysis with 676,000 individuals elucidates the association of polygenic risk scores of complex traits with human lifespan
S. Sakaue, M. Kanai, J. Karjalainen, M. Akiyama +10 more
2020Nature Medicine108 citations Open access
Semantic Scholar
The impact of non-additive genetic associations on age-related complex diseases
Marta Guindo-Martínez, R. Amela, S. Bonàs-Guarch, Montserrat Puiggròs +17 more
2020Nature Communications107 citations Open access
Semantic Scholar
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population
M. Kurki, J. Karjalainen, P. Palta, Timo P. Sipilä +164 more
2023Nature95 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
Mono- and biallelic variant effects on disease at biobank scale
H. Heyne, J. Karjalainen, K. Karczewski, S. Lemmelä +7 more
2023Nature86 citations Open access
Semantic Scholar
The impact of rare protein coding genetic variation on adult cognitive function
Chia-Yen Chen, Ruo-Yu Tian, Tian Ge, Max Lam +74 more
2022Nature Genetics62 citations Open access
Semantic Scholar
A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine
Yanjun Guo, P. Rist, I. Daghlas, F. Giulianini +129 more
2020Nature Communications61 citations Open access
Semantic Scholar
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders
Dennis Lal, P. May, E. Pérez-Palma, K. Samocha +27 more
2020Genome Medicine61 citations Open access
Semantic Scholar
CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum
Enrico D H Konrad, Niels Nardini, A. Caliebe, I. Nagel +59 more
2019Genetics in Medicine55 citations Open access
Semantic Scholar
The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia
R. Nehme, O. Pietiläinen, M. Artomov, M. Tegtmeyer +41 more
2021Nature Communications54 citations Open access
Semantic Scholar
A causal effects of gut microbiota in the development of migraine
Qiang He, Wenjing Wang, Yang Xiong, Chuan-Yuan Tao +69 more
2023The Journal of Headache and Pain47 citations Open access
Semantic Scholar
Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland
M. Kurki, E. Saarentaus, O. Pietiläinen, P. Gormley +22 more
2019Nature Communications46 citations Open access
Semantic Scholar
Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache
Katherine M. Siewert, D. Klarin, S. Damrauer, Kyong-Mi Chang +130 more
2020International Journal of Epidemiology45 citations Open access
Semantic Scholar
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
Erik L. Bao, Satish K. Nandakumar, Xiaotian Liao, A. Bick +335 more
2020Nature44 citations Open access
Semantic Scholar
Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks
Rounak Dey, Wei Zhou, T. Kiiskinen, A. Havulinna +9 more
2022Nature Communications42 citations Open access
Semantic Scholar
Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases
T. Kiiskinen, P. Helkkula, Kristi Krebs, J. Karjalainen +24 more
2023Nature Medicine28 citations Open access
Semantic Scholar
Causal relationships between migraine and microstructural white matter: a Mendelian randomization study
Lei Zhao, Wenhui Zhao, V. Anttila, V. Artto +66 more
2023The Journal of Headache and Pain26 citations Open access
Semantic Scholar
Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration.
Joel T. Rämö, E. Abner, E. C. van Dijk, Xin Wang +24 more
2023JAMA ophthalmology24 citations Open access
Semantic Scholar
High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene
F. Rahimov, Pekka Nieminen, P. Kumari, E. Juuri +24 more
2024Nature Communications22 citations Open access
Semantic Scholar
Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population
P. Helkkula, S. Hassan, E. Saarentaus, E. Vartiainen +7 more
2023Communications Biology22 citations Open access
Semantic Scholar
Recessive Genome-wide Meta-analysis Illuminates Genetic Architecture of Type 2 Diabetes.
M. O'Connor, Philip H. Schroeder, A. Huerta-Chagoya, Paula Cortés-Sánchez +16 more
2021Diabetes22 citations Open access
Semantic Scholar
A global atlas of genetic associations of 220 deep phenotypes
S. Sakaue, M. Kanai, Yosuke Tanigawa, J. Karjalainen +43 more
2020medRxiv22 citations Open access
Semantic Scholar
Aneurysm Size is the Strongest Risk Factor for Intracranial Aneurysm Growth in the Eastern Finnish Population.
Joel Björkman, J. Frösén, Olli I. Tähtinen, T. Huttunen +7 more
2019Neurosurgery20 citations
Semantic Scholar
Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata
E. Sliz, J. Tyrmi, N. Rahmioglu, K. Zondervan +323 more
2023Nature Communications18 citations Open access
Semantic Scholar
Major Genetic Risk Factors for Dupuytren's Disease Are Inherited From Neandertals
Richard Ågren, S. Patil, Xiang Zhou, A. Palotie +325 more
2023Molecular biology and evolution17 citations Open access
Semantic Scholar
Polygenic and clinical risk scores and their impact on age at onset of cardiometabolic diseases and common cancers
N. Mars, J. Koskela, P. Ripatti, T. Kiiskinen +12 more
2019bioRxiv17 citations Open access
Semantic Scholar
Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis
S. Ruotsalainen, I. Surakka, N. Mars, J. Karjalainen +16 more
2022Communications Biology16 citations Open access
Semantic Scholar
Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations
V. Salo, J. Määttä, E. Sliz, A. Palotie +332 more
2023medRxiv15 citations Open access
Semantic Scholar
Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure
Joel T. Rämö, T. Kiiskinen, Richard Seist, Kristi Krebs +20 more
2023Nature Communications15 citations Open access
Semantic Scholar
A novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development
Elisa J. Rahikkala, L. Urpa, B. Ghimire, Hande Topa +16 more
2022European Journal of Human Genetics15 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 Neurodegeneration14 citations Open access
Semantic Scholar
Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals
E. Bosch, B. Popp, Esther Güse, C. Skinner +68 more
2023medRxiv14 citations Open access
Semantic Scholar
Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants
E. Saarentaus, A. Havulinna, N. Mars, Ari V. Ahola-Olli +16 more
2021Molecular Psychiatry14 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
Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population
Daniel L. Polla, Elisa J. Rahikkala, Michaela K. Bode, T. Määttä +15 more
2019European Journal of Human Genetics13 citations Open access
Semantic Scholar
NTHL1 is a recessive cancer susceptibility gene
Anna K. Nurmi, L. Pelttari, J. Kiiski, Sofia Khan +333 more
2023Scientific Reports11 citations Open access
Semantic Scholar
Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia
A. Lokki, M. Triebwasser, E. Daly, S. Heinonen +13 more
2024Genes and Immunity10 citations Open access
Semantic Scholar
Identification of 64 new risk loci for major depression, refinement of the genetic architecture and risk prediction of recurrence and comorbidities
T. Als, M. Kurki, J. Grove, G. Voloudakis +38 more
2022medRxiv10 citations Open access
Semantic Scholar
Diabetes is associated with familial idiopathic normal pressure hydrocephalus: a case–control comparison with family members
Joel Räsänen, J. Huovinen, V. Korhonen, A. Junkkari +18 more
2020Fluids and Barriers of the CNS10 citations Open access
Semantic Scholar

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A. Palotie×41
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A. Palotie — researcher profile on SciRah
J. Karjalainen×21
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J. Karjalainen — researcher profile on SciRah
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P. Palta — researcher profile on SciRah
T. Kiiskinen×18
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S. Ripatti — researcher profile on SciRah

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N. Mars — researcher profile on SciRah

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M. Kaunisto×12

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M. Kaunisto — researcher profile on SciRah

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S. Ruotsalainen — researcher profile on SciRah