Chaudhari BP - Search Results

1

Promises and challenges of genomic newborn screening (NBS) - lessons from public health NBS programs.

Mori M, Chaudhari BP, Ream MA, Kemper AR. Mori M, et al. Among authors: chaudhari bp. Pediatr Res. 2024 Nov 8. doi: 10.1038/s41390-024-03689-0. Online ahead of print. Pediatr Res. 2024. PMID: 39516573 Review.

2

Perinatal-lethal nonimmune fetal hydrops attributed to MECOM-associated bone marrow failure.

Dash CA, Madden JA, Cummings C, Rose M, Wilson SD, Mori M, Agrawal PB, Chaudhari BP, Wojcik MH. Dash CA, et al. Among authors: chaudhari bp. Cold Spring Harb Mol Case Stud. 2023 Jul 11;9(3):a006289. doi: 10.1101/mcs.a006289. Print 2023 Jun. Cold Spring Harb Mol Case Stud. 2023. PMID: 37230770 Free PMC article.

3

A pediatric perspective on genomics and prevention in the twenty-first century.

Chaudhari BP, Manickam K, McBride KL. Chaudhari BP, et al. Pediatr Res. 2020 Jan;87(2):338-344. doi: 10.1038/s41390-019-0597-z. Epub 2019 Oct 2. Pediatr Res. 2020. PMID: 31578042 Review.

4

Neurogenetic and Metabolic Mimics of Common Neonatal Neurological Disorders.

Burns W, Chaudhari BP, Haffner DN. Burns W, et al. Among authors: chaudhari bp. Semin Pediatr Neurol. 2022 Jul;42:100972. doi: 10.1016/j.spen.2022.100972. Epub 2022 Apr 18. Semin Pediatr Neurol. 2022. PMID: 35868729

5

Congenital Brain Malformations: An Integrated Diagnostic Approach.

Chaudhari BP, Ho ML. Chaudhari BP, et al. Semin Pediatr Neurol. 2022 Jul;42:100973. doi: 10.1016/j.spen.2022.100973. Epub 2022 Apr 22. Semin Pediatr Neurol. 2022. PMID: 35868725 Review.

6

Genetic testing for diffuse lung diseases in children.

Hamvas A, Chaudhari BP, Nogee LM. Hamvas A, et al. Among authors: chaudhari bp. Pediatr Pulmonol. 2024 Sep;59(9):2286-2297. doi: 10.1002/ppul.26447. Epub 2023 May 16. Pediatr Pulmonol. 2024. PMID: 37191361 Review.

7

Ethical and Legal Issues Surrounding Genetic Testing in the NICU.

Callahan KP, Clayton EW, Lemke AA, Chaudhari BP, Wenger TL, Lyle ANJ, Brothers KB. Callahan KP, et al. Among authors: chaudhari bp. Neoreviews. 2024 Mar 1;25(3):e127-e138. doi: 10.1542/neo.25-3-e127. Neoreviews. 2024. PMID: 38425196

8

Provision and availability of genomic medicine services in Level IV neonatal intensive care units.

Wojcik MH, Callahan KP, Antoniou A, Del Rosario MC, Brunelli L, ElHassan NO, Gogcu S, Murthy K, Rumpel JA, Wambach JA, Suhrie K, Fishler K, Chaudhari BP. Wojcik MH, et al. Among authors: chaudhari bp. Genet Med. 2023 Oct;25(10):100926. doi: 10.1016/j.gim.2023.100926. Epub 2023 Jul 6. Genet Med. 2023. PMID: 37422715 Free PMC article.

9

Hypomorphic alleles pose challenges in rare disease genomic variant interpretation.

Nolan DK, Chaudhari B, Franklin SJ, Wijeratne S, Pfau R, Mihalic Mosher T, Crist E, McBride KL, White P, Wilson RK, Hickey SE, Koboldt DC. Nolan DK, et al. Clin Genet. 2021 Dec;100(6):775-776. doi: 10.1111/cge.14052. Epub 2021 Sep 3. Clin Genet. 2021. PMID: 34476810

10

NeoGx: Machine-Recommended Rapid Genome Sequencing for Neonates.

Antoniou AA, McGinley R, Metzler M, Chaudhari BP. Antoniou AA, et al. Among authors: chaudhari bp. medRxiv [Preprint]. 2024 Jun 25:2024.06.24.24309403. doi: 10.1101/2024.06.24.24309403. medRxiv. 2024. PMID: 38978650 Free PMC article. Preprint.

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