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Nonsense Variant PRDM16-Q187X Causes Impaired Myocardial Development and TGF-β Signaling Resulting in Noncompaction Cardiomyopathy in Humans and Mice.
Sun B, Rouzbehani OMT, Kramer RJ, Ghosh R, Perelli RM, Atkins S, Fatahian AN, Davis K, Szulik MW, Goodman MA, Hathaway MA, Chi E, Word TA, Tunuguntla H, Denfield SW, Wehrens XHT, Whitehead KJ, Abdelnasser HY, Warren JS, Wu M, Franklin S, Boudina S, Landstrom AP. Sun B, et al. Among authors: whitehead kj. Circ Heart Fail. 2023 Dec;16(12):e010351. doi: 10.1161/CIRCHEARTFAILURE.122.010351. Epub 2023 Dec 19. Circ Heart Fail. 2023. PMID: 38113297
De Novo Brain Vascular Malformations in Hereditary Hemorrhagic Telangiectasia.
Beslow LA, Krings T, Kim H, Hetts SW, Lawton MT, Ratjen F, Whitehead KJ, Gossage JR, McCulloch CE, Clancy M, Bagheri N, Faughnan ME; Brain Vascular Malformation Consortium HHT Investigator Group. Beslow LA, et al. Among authors: whitehead kj. Pediatr Neurol. 2024 Mar 22;155:120-125. doi: 10.1016/j.pediatrneurol.2024.03.013. Online ahead of print. Pediatr Neurol. 2024. PMID: 38631080
Brain AVM compactness score in children with hereditary hemorrhagic telangiectasia.
Beslow LA, Vossough A, Kim H, Nelson J, Lawton MT, Pollak J, Lin DDM, Ratjen F, Hammill AM, Hetts SW, Gossage JR, Whitehead KJ, Faughnan ME, Krings T; Brain Vascular Malformation Consortium HHT Investigator Group. Beslow LA, et al. Among authors: whitehead kj. Childs Nerv Syst. 2024 Mar 22. doi: 10.1007/s00381-024-06366-z. Online ahead of print. Childs Nerv Syst. 2024. PMID: 38517485
Reply to Eker et al. Comment on "Kilian et al. Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. J. Clin. Med. 2023, 12, 2704".
Kilian A, Latino GA, White AJ, Ratjen F, McDonald J, Whitehead KJ, Gossage JR, Krings T, Lawton MT, Kim H, Faughnan ME, The Brain Vascular Malformation Consortium Hht Investigator Group. Kilian A, et al. Among authors: whitehead kj. J Clin Med. 2023 Dec 1;12(23):7462. doi: 10.3390/jcm12237462. J Clin Med. 2023. PMID: 38068512 Free PMC article.
The association between BRAF-V600E mutations and death from thin (≤1.00 mm) melanomas: A nested case-case study from Queensland, Australia.
Claeson M, Tan SX, Lambie D, Brown S, Walsh MD, Baade PD, Pandeya N, Whitehead KJ, Soyer HP, Smithers BM, Whiteman DC, Khosrotehrani K. Claeson M, et al. Among authors: whitehead kj. J Eur Acad Dermatol Venereol. 2023 Sep;37(9):e1168-e1172. doi: 10.1111/jdv.19173. Epub 2023 May 16. J Eur Acad Dermatol Venereol. 2023. PMID: 37147869 No abstract available.
Choroidal melanoma with synchronous Fuchs' adenoma and novel ATRX mutation.
Harford E, Palmer JM, Glasson WJ, Warrier SK, Whitehead KJ, Brooks KM, Johansson PA, Hayward NK, McGrath LA. Harford E, et al. Among authors: whitehead kj. Int J Retina Vitreous. 2022 Apr 1;8(1):24. doi: 10.1186/s40942-022-00374-4. Int J Retina Vitreous. 2022. PMID: 35365243 Free PMC article.
81 results