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Cold Spring Harbor Symposia on Quantitative Biology|March 27, 2007
Small RNA regulators and the bacterial response to stressS Gottesman, C A McCullen, M Guillier, et al.Clinical Case Reports|June 8, 2017
Acromelia-oligodontia syndromeJyothirmai Talasila, Ramaswamy Pachigolla, Kiranmai V S N Yarlagadda, et al.The Journal of Clinical Endocrinology and Metabolism|November 6, 2021
Health Care Transition From Pediatric- to Adult-Focused Care in X-linked Hypophosphatemia: Expert ConsensusKathryn Dahir, Ruban Dhaliwal, Jill Simmons, et al.Bone|May 16, 2019
New explanation for autosomal dominant high bone mass: Mutation of low-density lipoprotein receptor-related protein 6Michael P Whyte, William H McAlister, Fan Zhang, et al.American Journal of Medical Genetics. Part A|November 9, 2011
Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin AFuki M Hisama, Davor Lessel, Dru Leistritz, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 23, 2018
Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25-Dihydroxyvitamin D-Mediated Hypercalcemia and Generalized OsteosclerosisMichael P Whyte, Emilina Lim, William H McAlister, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 14, 2012
Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancyJesse E Otero, Gary S Gottesman, William H McAlister, et al.Bone|July 31, 2024
Transmembrane protein 53 craniotubular dysplasia (OMIM # 619727): The skeletal disease and consequent blindness of this new disorderMichael P Whyte, Robert S Weinstein, Paul H Phillips, et al.NEJM Evidence|May 21, 2024
Broadening Eligibility Criteria and Diversity among Patients for Cancer Clinical TrialsManeet Kaur, Filip Frahm, Yichen Lu, et al.Bone|April 17, 2020
Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7)Michael P Whyte, Philippe M Campeau, William H McAlister, et al.Pageof 14