Publications by authors named "Kumar Veerapen"

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Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses.
Thomas D Als, Mitja I Kurki, Jakob Grove, Georgios Voloudakis, Karen Therrien, Kumar Veerapen

Nat Med· July 2023

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Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.
Mitja I Kurki, Juha Karjalainen, Priit Palta, Timo P Sipilä, Kati Kristiansson, Kumar Veerapen

Nature· March 2023

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Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases.
Tuomo Kiiskinen, Pyry Helkkula, Kristi Krebs, Juha Karjalainen, Elmo Saarentaus, Kumar Veerapen

Nat Med· January 2023

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FinnGen provides genetic insights from a well-phenotyped isolated population.
Mitja I Kurki, Juha Karjalainen, Priit Palta, Timo P Sipilä, Kati Kristiansson, Kumar Veerapen

Nature· January 2023

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Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.
Guillaume Butler-Laporte, Gundula Povysil, Jack A Kosmicki, Elizabeth T Cirulli, Theodore Drivas, Kumar Veerapen

PLoS Genet· November 2022

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Genetic variations in methotrexate metabolic pathway genes influence methotrexate responses in rheumatoid arthritis patients in Malaysia.
Hong Xi Sha, Kumar Veerapen, Sook Khuan Chow, Suk Chyn Gun, Ing Soo Lau

Sci Rep· July 2022

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Recessive Genome-Wide Meta-analysis Illuminates Genetic Architecture of Type 2 Diabetes.
Mark J O'Connor, Philip Schroeder, Alicia Huerta-Chagoya, Paula Cortés-Sánchez, Silvía Bonàs-Guarch, Kumar Veerapen

Diabetes· March 2022

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Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.
Padhraig Gormley, Mitja I Kurki, Marjo Eveliina Hiekkala, Kumar Veerapen, Paavo Häppölä

Neuron· September 2018

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Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.
Padhraig Gormley, Mitja I Kurki, Marjo Eveliina Hiekkala, Kumar Veerapen, Paavo Häppölä

Neuron· May 2018

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