Suchergebnisse - "McCarthy, Shane E"

PubPharm (25)

1

Casirivimab and Imdevimab Treatment Reduces Viral Load and Improves Clinical Outcomes in Seropositive Hospitalized COVID-19 Patients with Nonneutralizing or Borderline Neutralizing Antibodies

enthalten in: mBio | 2022

von Hooper, A. | Somersan-Karakaya, S. | McCarthy, S. | +12

2

Casirivimab and Imdevimab Treatment in Seropositive, Hospitalized COVID-19 Patients With Non-neutralizing or Borderline Neutralizing Antibodies

enthalten in: bioRxiv.org | 2022

von Hooper, A. | Somersan-Karakaya, S. | McCarthy, S. | +11

3

Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease

enthalten in: Nature genetics | 2022

von Horowitz, J. | Kosmicki, J. | Damask, A. | +157

UpdateOf: medRxiv. 2021 Jun 10;:. - PMID 33619501

4

Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals

enthalten in: American journal of human genetics | 2021

von Kosmicki, J. | Horowitz, J. | Banerjee, N. | +80

5

Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia

enthalten in: bioRxiv.org | 2020

von Teng, S. | Thomson, P. | McCarthy, S. | +16

6

Profiling and leveraging relatedness in a precision medicine cohort of 92,455 exomes

enthalten in: bioRxiv.org | 2020

von Staples, J. | Maxwell, E. | Gosalia, N. | +24

7

Detection of rare disease-related genetic variants using the birthday model

enthalten in: bioRxiv.org | 2019

von Berstein, Y. | McCarthy, S. | Kramer, M. | +1

8

Profiling copy number variation and disease associations from 50,726 DiscovEHR Study exomes

enthalten in: bioRxiv.org | 2019

von Maxwell, E. | Packer, J. | O’Dushlaine, C. | +35

9

KaryoScan: abnormal karyotype detection from whole-exome sequence

enthalten in: bioRxiv.org | 2019

von Maxwell, E. | Gonzaga-Jauregui, C. | McCarthy, S. | +14

10

Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

enthalten in: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2019

von Harold, D. | Connolly, S. | Riley, B. | +113