Center-Authored Papers

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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
Snyder MW, Simmons LE, Kitzman JO, Coe BP, Henson JM, Daza RM, Eichler EE, Shendure J, Gammill HS.  2015.  Copy-number variation and false positive prenatal aneuploidy screening results.. The New England journal of medicine. 372(17):1639-45. Abstract
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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
Koolen DA, Pfundt R, Linda K, Beunders G, Veenstra-Knol HE, Conta JH, Fortuna AM, Gillessen-Kaesbach G, Dugan S, Halbach S et al..  2015.  The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant.. European journal of human genetics : EJHG. Abstract
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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
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Helsmoortel C, Vulto-van Silfhout AT, Coe BP, Vandeweyer G, Rooms L, van den Ende J, Schuurs-Hoeijmakers JHM, Marcelis CL, Willemsen MH, Vissers LELM et al..  2014.  A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP.. Nature genetics. Abstract
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Fox K, Johnsen JM, Coe BP, Frazar CD, Reiner AP, Eichler EE, Nickerson DA.  2016.  Analysis of exome sequencing data sets reveals structural variation in the coding region of ABO in individuals of African ancestry.. Transfusion. Abstract
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Cooper GM, Coe BP, Girirajan S, Rosenfeld JA, Vu TH, Baker C, Williams C, Stalker H, Hamid R, Hannig V et al..  2011.  A copy number variation morbidity map of developmental delay.. Nature genetics. 43(9):838-46. Abstract
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Bernier R, Golzio C, Xiong B, Stessman HA, Coe BP, Penn O, Witherspoon K, Gerdts J, Baker C, Vulto-van Silfhout AT et al..  2014.  Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development.. Cell. Abstract