(Q36757756)

English

Determining the effects and challenges of incorporating genetic testing into primary care management of hypertensive patients with African ancestry

scientific article published on 30 December 2015

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Determining the effects and challenges of incorporating genetic testing into primary care management of hypertensive patients with African ancestry (English)

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

author name string

C R Horowitz

1

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

N S Abul-Husn

2

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

S Ellis

3

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

M A Ramos

4

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

R Negron

5

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

M Suprun

6

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

R E Zinberg

7

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

T Sabin

8

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

D Hauser

9

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

N Calman

10

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

E Bagiella

11

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

E P Bottinger

12

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

language of work or name

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publication date

30 December 2015

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Contemporary Clinical Trials

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

47

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

101-108

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record

1 reference

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Physician Attitudes toward Adopting Genome-Guided Prescribing through Clinical Decision Support

1 reference

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Physicians' knowledge, beliefs, and use of race and human genetic variation: new measures and insights

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APOL1 risk variants, race, and progression of chronic kidney disease

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Incorporating direct-to-consumer genomic information into patient care: attitudes and experiences of primary care physicians

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APOL1 variants associate with increased risk of CKD among African Americans

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The CLIPMERGE PGx Program: clinical implementation of personalized medicine through electronic health records and genomics-pharmacogenomics

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Implementing genomic medicine in the clinic: the future is here

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Initial validation of a self-report measure of the extent of and reasons for medication nonadherence.

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Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans

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Attitudes and practices among internists concerning genetic testing

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Finding a place for genomics in health disparities research.

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Population-based risk assessment of APOL1 on renal disease.

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Racial and ethnic differences in kidney function decline among persons without chronic kidney disease

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Association of trypanolytic ApoL1 variants with kidney disease in African Americans

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Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene

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Community-based participatory research from the margin to the mainstream: are researchers prepared?

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The success of recruiting minorities, women, and elderly into a randomized controlled effectiveness trial

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Insurance type and minority status associated with large disparities in prelisting dialysis among candidates for kidney transplantation

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The association between life chaos, health care use, and health status among HIV-infected persons

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A roadmap for national action on clinical decision support

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Unraveling the racial disparities associated with kidney disease

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Public experiences, knowledge and expectations about medical genetics and the use of genetic information.

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Apolipoprotein L-I is the trypanosome lytic factor of human serum

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Identifiers

10.1016/J.CCT.2015.12.020

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

ResearchGate publication ID

0 references

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