Boston Children's Hospital

Hospital


Location: Boston, MA, United States (USA) (US) US

ISNI: 0000000403788438

ROR: https://ror.org/00dvg7y05

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

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Abstract

Journal

Arthritis flares mediated by tissue-resident memory T cells in the joint (2021) Chang MH, Levescot A, Nelson-Maney N, Blaustein RB, Winden KD, Morris A, Wactor A, et al. Journal article Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss (2021) Richard EM, Bakhtiari S, Marsh AP, Kaiyrzhanov R, Wagner M, Shetty S, Pagnozzi A, et al. Journal article What every reader should know about studies using electronic health record data but may be afraid to ask (2021) Kohane IS, Aronow BJ, Avillach P, Beaulieu-Jones BK, Bellazzi R, Bradford RL, Brat GA, et al. Journal article, Review article Pontocerebellar hypoplasia due to bi-allelic variants in MINPP1 (2021) Appelhof B, Wagner M, Hoefele J, Heinze A, Roser T, Koch-Hogrebe M, Roosendaal SD, et al. Journal article Odontoblast TRPC5 channels signal cold pain in teeth (2021) Bernal L, Sotelo-Hitschfeld P, König C, Sinica V, Wyatt A, Winter Z, Hein A, et al. Journal article Automated detection and staging of malaria parasites from cytological smears using convolutional neural networks. (2021) Davidson MS, Andradi-Brown C, Yahiya S, Chmielewski J, O’Donnell AJ, Gurung P, Jeninga M, et al. Journal article Clinical, neuroimaging, and molecular spectrum of TECPR2-associated hereditary sensory and autonomic neuropathy with intellectual disability (2021) Neuser S, Brechmann B, Heimer G, Broesse I, Schubert S, O'Grady L, Zech M, et al. Journal article Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype (2021) Zanoni P, Steindl K, Sengupta D, Joset P, Bahr A, Sticht H, Lang-Muritano M, et al. Journal article Toward a better definition of focal cortical dysplasia: An iterative histopathological and genetic agreement trial (2021) Blümcke I, Coras R, Busch RM, Morita-Sherman M, Lal D, Prayson R, Cendes F, et al. Journal article Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior (2021) Harris HK, Nakayama T, Lai J, Zhao B, Argyrou N, Gubbels CS, Soucy A, et al. Journal article
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