Skip Nav Destination
Close Modal
Update search
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
NARROW
Format
Subjects
Journal
Article Type
Date
Availability
1-2 of 2
Keywords: Family samples
Close
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Sort by
Journal Articles
Subject Area:
Genetics
Qi Yan, Daniel E. Weeks, Hemant K. Tiwari, Nengjun Yi, Kui Zhang, Guimin Gao, Wan-Yu Lin, Xiang-Yang Lou, Wei Chen, Nianjun Liu
Journal:
Human Heredity
Hum Hered (2016) 80 (3): 126–138.
Published Online: 29 April 2016
...-variant test does not currently exist for longitudinal data from family samples. Therefore, in this paper, we aim to introduce an association test for rare variants, which includes multiple longitudinal phenotype measurements for either population or family samples. Methods: This approach uses KM...
Journal Articles
Subject Area:
Genetics
Qi Yan, Hemant K. Tiwari, Nengjun Yi, Guimin Gao, Kui Zhang, Wan-Yu Lin, Xiang-Yang Lou, Xiangqin Cui, Nianjun Liu
Journal:
Human Heredity
Hum Hered (2015) 79 (2): 60–68.
Published Online: 10 March 2015
...Qi Yan; Hemant K. Tiwari; Nengjun Yi; Guimin Gao; Kui Zhang; Wan-Yu Lin; Xiang-Yang Lou; Xiangqin Cui; Nianjun Liu Objective: The existing methods for identifying multiple rare variants underlying complex diseases in family samples are underpowered. Therefore, we aim to develop a new set-based...
