Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with AutismStephan Sanders, Shrikant Mane, A. Gulhan Ercan‐Sencicek et al.|Neuron|2011Cited by 1.3k
K <sup>+</sup> Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary HypertensionMurim Choi, Richard P. Lifton, Ute I. Scholl et al.|Science|2011Cited by 983
De novo mutations in histone-modifying genes in congenital heart diseaseSamir Zaidi, Richard P. Lifton, Murim Choi et al.|Nature|2013Cited by 958
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalitiesLynn M. Boyden, Richard P. Lifton, Murim Choi et al.|Nature|2012Cited by 631
Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronismUte I. Scholl, Richard P. Lifton, Gerald Goh et al.|Nature Genetics|2013Cited by 621