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1.
Genetic variation associated with circulating monocyte count in the eMERGE Network.
Hum Mol Genet
; 22(10): 2119-27, 2013 May 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-23314186
2.
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.
Am J Hum Genet
; 89(4): 529-42, 2011 Oct 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-21981779
3.
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.
Hum Genet
; 131(4): 639-52, 2012 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-22037903
4.
Confirmation of the reported association of clonal chromosomal mosaicism with an increased risk of incident hematologic cancer.
PLoS One
; 8(3): e59823, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23533652
5.
Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records.
PLoS One
; 8(6): e63481, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23762230
6.
Analyzing the heterogeneity and complexity of Electronic Health Record oriented phenotyping algorithms.
AMIA Annu Symp Proc
; 2011: 274-83, 2011.
Artículo
en Inglés
| MEDLINE | ID: mdl-22195079
7.
Electronic medical records for genetic research: results of the eMERGE consortium.
Sci Transl Med
; 3(79): 79re1, 2011 Apr 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-21508311
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