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Kurki, Mitja I
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1

Evidence for the additivity of rare and common variant burd..:

Urpa, Lea ; Kurki, Mitja I. ; Rahikkala, Elisa...
European Journal of Human Genetics.  32 (2024)  5 - p. 576-583 , 2024
Link: https://doi.org/10.1038/..
 
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2

FinnGen provides genetic insights from a well-phenotyped is..:

Kurki, Mitja I. ; Karjalainen, Juha ; Palta, Priit...
Nature.  613 (2023)  7944 - p. 508-518 , 2023
Link: https://doi.org/10.1038/..
 
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3

Novel patients with NHLRC2 variants expand the phenotypic s..:

Tallgren, Antti ; Kager, Leo ; O'Grady, Gina...
Frontiers in Neuroscience.  17 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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4

Author Correction: FinnGen provides genetic insights from a..:

Kurki, Mitja I. ; Karjalainen, Juha ; Palta, Priit...
Nature.  615 (2023)  7952 - p. E19-E19 , 2023
Link: https://doi.org/10.1038/..
 
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5

Depression pathophysiology, risk prediction of recurrence a..:

Als, Thomas D. ; Kurki, Mitja I. ; Grove, Jakob...
Nature Medicine.  29 (2023)  7 - p. 1832-1844 , 2023
Link: https://doi.org/10.1038/..
 
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6

A novel variant in SMG9 causes intellectual disability, con..:

Rahikkala, Elisa ; Urpa, Lea ; Ghimire, Bishwa...
European Journal of Human Genetics.  30 (2022)  5 - p. 619-627 , 2022
Link: https://doi.org/10.1038/..
 
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7

Genetic associations of protein-coding variants in human di..:

Sun, Benjamin B. ; Kurki, Mitja I. ; Foley, Christopher N....
Nature.  603 (2022)  7899 - p. 95-102 , 2022
Link: https://doi.org/10.1038/..
 
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8

Diabetes is associated with familial idiopathic normal pres..:

Räsänen, Joel ; Huovinen, Joel ; Korhonen, Ville E....
Fluids and Barriers of the CNS.  17 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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9

Contribution of rare and common variants to intellectual di..:

Kurki, Mitja I. ; Saarentaus, Elmo ; Pietiläinen, Olli...
Nature Communications.  10 (2019)  1 - p. , 2019
Link: https://doi.org/10.1038/..
 
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10

Prevalence of Schizophrenia in Idiopathic Normal Pressure H..:

Vanhala, Vasco ; Junkkari, Antti ; Korhonen, Ville E...
Neurosurgery.  84 (2019)  4 - p. 883-889 , 2019
Link: https://doi.org/10.1093/..
 
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11

A multiomic approach to characterize the temporal sequence ..:

Marttinen, Mikael ; Paananen, Jussi ; Neme, Antonio...
Neurobiology of Disease.  124 (2019)  - p. 454-468 , 2019
Link: https://doi.org/10.1016/..
 
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12

Impact of constitutional TET2 haploinsufficiency on molecul..:

Kaasinen, Eevi ; Kuismin, Outi ; Rajamäki, Kristiina...
Nature Communications.  10 (2019)  1 - p. , 2019
Link: https://doi.org/10.1038/..
 
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13

Biallelic loss-of-function P4HTM gene variants cause hypoto..:

Rahikkala, Elisa ; Myllykoski, Matti ; Hinttala, Reetta...
Genetics in Medicine.  21 (2019)  10 - p. 2355-2363 , 2019
Link: https://doi.org/10.1038/..
 
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14

Secondary hypertension in patients with saccular intracrani..:

Kotikoski, Satu ; Huttunen, Jukka ; Huttunen, Terhi J....
PLOS ONE.  13 (2018)  10 - p. e0206432 , 2018
Link: https://doi.org/10.1371/..
 
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15

Common Variant Burden Contributes to the Familial Aggregati..:

Gormley, Padhraig ; Kurki, Mitja I. ; Hiekkala, Marjo Eveliina...
Neuron.  98 (2018)  4 - p. 743-753.e4 , 2018
Link: https://doi.org/10.1016/..
 
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