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Unpublished / Preprint

Publication year

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Abstract

Journal

International comparisons of laboratory values from the 4CE collaborative to predict COVID-19 mortality (2022) Weber GM, Hong C, Xia Z, Palmer NP, Avillach P, L'Yi S, Keller MS, et al. Journal article Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract (2022) Wu CHW, Lim TY, Wang C, Seltzsam S, Zheng B, Schierbaum L, Schneider S, et al. Journal article The ILAE consensus classification of focal cortical dysplasia: An update proposed by an ad hoc task force of the ILAE diagnostic methods commission (2022) Najm I, Lal D, Alonso Vanegas M, Cendes F, Lopes-Cendes I, Palmini A, Paglioli E, et al. Journal article Beyond founder and truncting variants in TECPR2-associated disorder (2022) Neuser S, Brechmann B, Heimer G, Brosse I, Schubert S, O'Grady L, Zech M, et al. Conference contribution Hospitalizations Associated With Mental Health Conditions Among Adolescents in the US and France During the COVID-19 Pandemic. (2022) Gutierrez-Sacristan A, Serret-Larmande A, Hutch MR, Saez C, Aronow BJ, Bhatnagar S, Bonzel CL, et al. Journal article Identification of environmental factors that promote intestinal inflammation. (2022) Sanmarco LM, Chao CC, Wang YC, Kenison JE, Li Z, Rone JM, Rejano-Gordillo CM, et al. Journal article Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling (2022) Holtz AM, VanCoillie R, Vansickle EA, Carere DA, Withrow K, Torti E, Juusola J, et al. Journal article De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability (2021) Schalk A, Cousin MA, Challman TD, Wain KE, Powis Z, Minks K, Trimouille A, et al. Journal article Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders (2021) Mannucci I, Dang NDP, Huber H, Murry JB, Abramson J, Althoff T, Banka S, et al. Journal article Neocortical development and epilepsy: insights from focal cortical dysplasia and brain tumours (2021) Blümcke I, Budday S, Poduri A, Lal D, Kobow K, Baulac S Journal article, Review article
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