E-LIB Suche - Ergebnisse für: Marc S. Williams

1

Exome-wide analysis of the discovehr cohort reveals novel c..:

Pandi, M.-T. (Maria-Theodora) ; Williams, M.S. (Marc S.) ; Spek, P.J. (Peter) van der..
http://repub.eur.nl/pub/127379. , 2020

Link: http://repub.eur.nl/pub/..

2

Cost Effectiveness of Age-Specific Screening Intervals for ..:

Naber, S.K. (Steffie) ; Kuntz, K.M. (Karen) ; Henrikson, N.B. (Nora B.)...
http://repub.eur.nl/pub/103615. , 2018

Link: http://repub.eur.nl/pub/..

3

A picture is worth a thousand words: advancing the use of v..:

Salvati, Zachary M ; Rahm, Alanna Kulchak ; Williams, Marc S...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127322/. , 2023

Link: http://www.ncbi.nlm.nih...

4

Making inroads to precision medicine for the treatment of a..:

Yuriy Baglaenko ; Catriona Wagner ; Vijay G. Bhoj...
https://www.cambridge.org/core/product/identifier/S2752614323000145/type/journal_article. , 2023

Link: https://doi.org/10.1017/..

5

A picture is worth a thousand words: advancing the use of v..:

Zachary M. Salvati ; Alanna Kulchak Rahm ; Marc S. Williams...
https://doi.org/10.1186/s43058-023-00424-4. , 2023

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

6

Evaluation of the portability of computable phenotypes with..:

Pacheco, Jennifer A ; Rasmussen, Luke V ; Wiley, Ken...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9898520/. , 2023

Link: http://www.ncbi.nlm.nih...

7

Yield of Familial Hypercholesterolemia Genetic and Phenotyp..:

Samuel S. Gidding ; H. Lester Kirchner ; Andrew Brangan...
https://www.ahajournals.org/doi/10.1161/JAHA.123.030073. , 2023

Link: https://doi.org/10.1161/..

8

On the launch of Genetics in Medicine Open: Disseminating k..:

Robert G. Best ; Marc S. Williams
http://www.sciencedirect.com/science/article/pii/S2949774423007872. , 2023

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

9

Testing and Management of Iron Overload After Genetic Scree..:

Savatt, Juliann M ; Johns, Alicia ; Schwartz, Marci L. B...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10594145/. , 2023

Link: http://www.ncbi.nlm.nih...

10

Evaluation of the portability of computable phenotypes with..:

Jennifer A. Pacheco ; Luke V. Rasmussen ; Ken Wiley...
https://doi.org/10.1038/s41598-023-27481-y. , 2023

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

11

Yield of Familial Hypercholesterolemia Genetic and Phenotyp..:

Gidding, Samuel S ; Kirchner, H. Lester ; Brangan, Andrew...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356068/. , 2023

Link: http://www.ncbi.nlm.nih...

12

Association of Pathogenic Variants in Hereditary Cancer Gen..:

Zeng, Chenjie ; Bastarache, Lisa A ; Tao, Ran...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026237/. , 2022

Link: http://www.ncbi.nlm.nih...

13

GA4GH: International policies and standards for data sharin..:

Rehm, Heidi L ; Page, Angela JH ; Smith, Lindsay...
https://www.repository.cam.ac.uk/handle/1810/334447. , 2022

Link: https://www.repository.c..

14

Population-based screening of newborns: Findings from the n..:

Kee Chan ; Amy Brower ; Marc S. Williams
https://www.frontiersin.org/articles/10.3389/fgene.2022.867354/full. , 2022

Link: https://doi.org/10.3389/..

15

The clinical utility of polygenic risk scores in genomic me..:

Kumuthini, Judit ; Zick, Brittany ; Balasopoulou, Angeliki...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055005/. , 2022

Link: http://www.ncbi.nlm.nih...