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- 2024
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Mark
Genetic evidence for T-wave area from 12-lead electrocardiograms to monitor cardiovascular diseases in patients taking diabetes medications
2024) In Human Genetics(
- Contribution to journal › Article
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Mark
Genome-wide association and Mendelian randomization analysis provide insights into the shared genetic architecture between high-dimensional electrocardiographic features and ischemic heart disease
(
- Contribution to journal › Article
- 2023
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Mark
Sex differences of the shared genetic landscapes between type 2 diabetes and peripheral artery disease in East Asians and Europeans
(
- Contribution to journal › Article
- 2015
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Mark
Types and effects of protein variations.
(
- Contribution to journal › Article
- 2014
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Mark
A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer
(
- Contribution to journal › Article
- 2013
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Mark
Genome-wide investigation of gene-environment interactions in colorectal cancer
(
- Contribution to journal › Article
- 2011
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Mark
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
- 2005
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Mark
Alport syndrome caused by inversion of a 21 Mb fragment of the long arm of the X-chromosome comprising exon 9 through 51 of the COL4A5 gene
(
- Contribution to journal › Article
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Mark
Book review: Genetic predisposition of cancer, 2nd ed.
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
- 2003
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Mark
Several interacting genes influence the malignant hyperthermia phenotype
(
- Contribution to journal › Article
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Mark
Book review: P.J. Morrison, S.V. Hodgson, N.E. Haites (eds): Familial breast cancer: genetics, screening and managementCambridge University Press, 2002, 401 pp, hardcover (ISBN 0-521-80373-X) pound 65.00.
(
- Contribution to journal › Article
- 2002
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Mark
A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes
(
- Contribution to journal › Article
- 2001
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Mark
Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity
(
- Contribution to journal › Article
- 2000
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Mark
Molecular genetic analysis of severe protein C deficiency
(
- Contribution to journal › Article
- 1999
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Mark
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells
(
- Contribution to journal › Article