Kelemen, Martin

Wellcome Sanger Institute

1 paper on CoChatORCID 0000-0002-4050-1817

Most cited papers

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Common genetic variants contribute to risk of rare severe neurodevelopmental disorders
Niemi, M. E. K., Martin, H. C., Rice, D. L., Gallone, G., Gordon, S., Kelemen, M., McAloney, K., McRae, J., Radford, E. J., Yu, S., et al. (2018) · Nature
Genetic Associations and EpidemiologyGenomics and Rare Diseases
Cited by 340

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