Suchergebnisse - "Abhyankar, Avinash"

PubPharm (93)

1

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

enthalten in: bioRxiv.org | 2024

von Abul-Husn, N. | Marathe, P. | Kelly, N. | +24

2

Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease

enthalten in: Circulation. Genomic and precision medicine | 2023

von Hays, T. | Hernan, R. | Disco, M. | +15

3

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2023

von Abul-Husn, N. | Marathe, P. | Kelly, N. | +24

UpdateOf: medRxiv. 2023 Mar 20;:. - PMID 36993157

4

Identification of copy number variants with genome sequencing : Clinical experiences from the NYCKidSeq program

enthalten in: Clinical genetics | 2023

von Bonini, K. | Thomas-Wilson, A. | Marathe, P. | +26

5

Implementation and Feasibility of Clinical Genome Sequencing Embedded Into the Outpatient Nephrology Care for Patients With Proteinuric Kidney Disease

enthalten in: Kidney international reports | 2023

von Marasa, M. | Ahram, D. | Rehman, A. | +22

6

Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function : A Meta-analysis of Community-Based Cohorts

enthalten in: Neurology | 2023

von Zhang, Y. | Liu, X. | Wiggins, K. | +143

7

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

enthalten in: medRxiv : the preprint server for health sciences | 2023

von Abul-Husn, N. | Marathe, P. | Kelly, N. | +24

UpdateIn: Genet Med. 2023 May 5;:100880. - PMID 37158195

8

Identification of copy number variants with genome sequencing : Clinical experiences from the NYCKidSeq program

enthalten in: Clinical Genetics | 2023

von Bonini, K. | Thomas‐Wilson, A. | Marathe, P. | +26

9

Implementation of Rapid Genome Sequencing for Infants with Congenital Heart Disease

enthalten in: bioRxiv.org | 2022

von Hays, T. | Hernan, R. | Disco, M. | +14

10

The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children

enthalten in: ResearchSquare.com | 2022

von Odgis, J. | Gallagher, K. | Suckiel, S. | +43

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