E-LIB Suche - Ergebnisse für: Spencer, Emily G.

1

The Coronavirus Disease 2019 Rebound Study: A Prospective C..:

Pandit, Jay A ; Radin, Jennifer M ; Chiang, Danielle C...
Clinical Infectious Diseases. 77 (2023) 1 - p. 25-31 , 2023

Link: https://doi.org/10.1093/..

2

Impact of polygenic risk communication: an observational mo..:

Muse, Evan D. ; Chen, Shang-Fu ; Liu, Shuchen...
npj Digital Medicine. 5 (2022) 1 - p. , 2022

Link: https://doi.org/10.1038/..

3

Direct to Consumer Fitness DNA Testing:

Topol, Eric J ; Spencer, Emily G
Clinical Chemistry. 65 (2019) 1 - p. 45-47 , 2019

Link: https://doi.org/10.1373/..

4

Re-analysis of whole-exome sequencing data uncovers novel d..:

Salfati, Elias L. ; Spencer, Emily G. ; Topol, Sarah E....
Genome Medicine. 11 (2019) 1 - p. , 2019

Link: https://doi.org/10.1186/..

5

Combined accelerometer and genetic analysis to differentiat..:

Molparia, Bhuvan ; Schrader, Brian N. ; Cohen, Eli...
PeerJ. 6 (2018) - p. e5308 , 2018

Link: https://doi.org/10.7717/..

6

Validation of a genetic risk score for atrial fibrillation:..:

Muse, Evan D. ; Wineinger, Nathan E. ; Spencer, Emily G....
PLOS Medicine. 15 (2018) 3 - p. e1002525 , 2018

Link: https://doi.org/10.1371/..

7

A feasibility study of colorectal cancer diagnosis via circ..:

Molparia, Bhuvan ; Oliveira, Glenn ; Wagner, Jennifer L....
PLOS ONE. 13 (2018) 5 - p. e0196826 , 2018

Link: https://doi.org/10.1371/..

8

Mutations of the mitochondrial carrier translocase channel ..:

Pacheu-Grau, David ; Callegari, Sylvie ; Emperador, Sonia...
Human Molecular Genetics. , 2018

Link: https://doi.org/10.1093/..

9

Mutation of WIF1: a potential novel cause of a Nail-Patella..:

Jones, Marilyn C. ; Topol, Sarah E. ; Rueda, Manuel...
Genetics in Medicine. 19 (2017) 10 - p. 1179-1183 , 2017

Link: https://doi.org/10.1038/..

10

Characterization of Greater Middle Eastern genetic variatio..:

Greater Middle East Variome Consortium ; Scott, Eric M ; Halees, Anason...
Nature Genetics. 48 (2016) 9 - p. 1071-1076 , 2016

Link: https://doi.org/10.1038/..

11

Mutations in KATNB1 Cause Complex Cerebral Malformations by..:

Mishra-Gorur, Ketu ; Çağlayan, Ahmet Okay ; Schaffer, Ashleigh E....
Neuron. 85 (2015) 1 - p. 228 , 2015

Link: https://doi.org/10.1016/..

12

Novel STAMBP mutation and additional findings in an Arabic ..:

Faqeih, Eissa A. ; Bastaki, Laila ; Rosti, Rasim Ozgur...
American Journal of Medical Genetics Part A. 167 (2015) 4 - p. 805-809 , 2015

Link: https://doi.org/10.1002/..

13

Mutations in KATNB1 Cause Complex Cerebral Malformations by..:

Mishra-Gorur, Ketu ; Çağlayan, Ahmet Okay ; Schaffer, Ashleigh E....
Neuron. 84 (2014) 6 - p. 1226-1239 , 2014

Link: https://doi.org/10.1016/..

14

Exome Sequencing Links Corticospinal Motor Neuron Disease t..:

Novarino, Gaia ; Fenstermaker, Ali G. ; Zaki, Maha S....
Science. 343 (2014) 6170 - p. 506-511 , 2014

Link: http://www.jstor.org/sta..

15

Genomic surveillance reveals dynamic shifts in the connecti..:

Matteson, Nathaniel L ; Hassler, Gabriel W ; Kurzban, Ezra...
qt1x4680vq. , 2023

Link: https://escholarship.org..