Center-Authored Papers

Filters: Author is Krumm, Niklas  [Clear All Filters]
2015
Krumm N, Turner TN, Baker C, Vives L, Mohajeri K, Witherspoon K, Raja A, Coe BP, Stessman HA, He Z-X et al..  2015.  Excess of rare, inherited truncating mutations in autism.. Nature genetics. Abstract
Sudmant PH, Mallick S, Nelson BJ, Hormozdiari F, Krumm N, Huddleston J, Coe BP, Baker C, Nordenfelt S, Bamshad M et al..  2015.  Global diversity, population stratification, and selection of human copy number variation.. Science (New York, N.Y.). Abstract
2014
Jacquemont S, Coe BP, Hersch M, Duyzend MH, Krumm N, Bergmann S, Beckmann JS, Rosenfeld JA, Eichler EE.  2014.  A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders.. American journal of human genetics. 94(3):415-25. Abstract
Hoischen A, Krumm N, Eichler EE.  2014.  Prioritization of neurodevelopmental disease genes by discovery of new mutations.. Nature neuroscience. 17(6):764-72. Abstract
Krumm N, O'Roak BJ, Shendure J, Eichler EE.  2014.  A de novo convergence of autism genetics and molecular neuroscience.. Trends in neurosciences. 37(2):95-105. Abstract