Self-Care Communication during Medical Encounters: Implications for Future Electronic Medical Records

Por Arar, Nedal H, Wang, Chen-Pin, Pugh, Jacqueline A
Publicado em 2006

Genetic variants in Transient Receptor Potential cation channel, subfamily M 1 (TRPM1) and their risk of albuminuria-related traits in Mexican Americans

Por Thameem, Farook, Puppala, Sobha, Arar, Nedal H., Blangero, John, Duggirala, Ravindranath, Abboud, Hanna E.
Publicado em 2011

Implementing Quality Improvement in Small, Autonomous Primary Care Practices: Implications for the Patient Centered Medical Home

Por Arar, Nedal H., Noel, Polly H., Leykum, Luci, Zeber, John E., Romero, Raquel, Parchman, Michael L.
Publicado em 2011

Endothelial Nitric Oxide Synthase (eNOS) gene polymorphisms and their association with Type 2 diabetes related traits in Mexican Americans

Por Thameem, Farook, Puppala, Sobha, Arar, Nedal H., Stern, Michael P., Blangero, John, Duggirala, Ravindranath, Abboud, Hanna E.
Publicado em 2008

Evaluation of Gremlin1 (GREM1) as a candidate susceptibility gene for albuminuria-related traits in Mexican Americans with Type 2 Diabetes

Por Thameem, Farook, Puppala, Sobha, He, Xin, Arar, Nedal H., Stern, Michael P., Blangero, John, Duggirala, Ravindranath, Abboud, Hanna E.
Publicado em 2009

A group randomized trial of a complexity-based organizational intervention to improve risk factors for diabetes complications in primary care settings: study protocol

Por Noel Polly H, Culler Steven D, Pugh Jacqueline A, Parchman Michael L, Arar Nedal H, Romero Raquel L, Palmer Raymond F
Publicado em 2008-03-01

A group randomized trial of a complexity-based organizational intervention to improve risk factors for diabetes complications in primary care settings: study protocol

Por Parchman, Michael L, Pugh, Jacqueline A, Culler, Steven D, Noel, Polly H, Arar, Nedal H, Romero, Raquel L, Palmer, Raymond F
Publicado em 2008

Genetic variants in the Renin-Angiotensin System genes are associated with Cardiovascular-Renal-related risk factors in Mexican Americans

Por Thameem, Farook, Voruganti, V. Saroja., He, Xin, Nath, Subrata D., Blangero, John, MacCluer, Jean W., Comuzzie, Anthony G., Abboud, Hanna E., Arar, Nedal H.
Publicado em 2008

The 27-bp repeat polymorphism in intron 4 (27 bp-VNTR) of endothelial nitric oxide synthase (eNOS) gene is associated with albumin to creatinine ratio in Mexican Americans

Por Nath, Subrata D., He, Xin, Voruganti, V. Saroja, Blangero, John, MacCluer, Jean W., Comuzzie, Anthony G., Arar, Nedal H., Abboud, Hanna E., Thameem, Farook
Publicado em 2009

A genome-wide search for linkage to chronic kidney disease in a community-based sample: the SAFHS

Por Arar, Nedal H., Voruganti, Venkata S., Nath, Subrata D., Thameem, Farook, Bauer, Richard, Cole, Shelley A., Blangero, John, MacCluer, Jean W., Comuzzie, Anthony G., Abboud, Hanna E.
Publicado em 2008

Evaluation of Polymorphisms in Paraoxonase 2 (PON2) Gene and Their Association with Cardiovascular-Renal Disease Risk in Mexican Americans

Por Thameem, Farook, He, Xin, Voruganti, V. Saroja, Nath, Subrata D., Fanti, Paolo, Blangero, John, MacCluer, Jean W., Comuzzie, Anthony G., Arar, Nedal H., Abboud, Hanna E.
Publicado em 2009

The Gly(972)Arg Variant of Human IRS1 Gene Is Associated With Variation in Glomerular Filtration Rate Likely Through Impaired Insulin Receptor Signaling

Por Thameem, Farook, Puppala, Sobha, Schneider, Jennifer, Bhandari, Basant, Arya, Rector, Arar, Nedal H., Vasylyeva, Tetyana L., Farook, Vidya S., Fowler, Sharon, Almasy, Laura, Blangero, John, Duggirala, Ravindranath, Abboud, Hanna E.
Publicado em 2012

Genetics of Variation in Serum Uric Acid and Cardiovascular Risk Factors in Mexican Americans

Por Voruganti, V. Saroja, Nath, Subrata D., Cole, Shelley A., Thameem, Farook, Jowett, Jeremy B., Bauer, Richard, MacCluer, Jean W., Blangero, John, Comuzzie, Anthony G., Abboud, Hanna E., Arar, Nedal H.
Publicado em 2009

Heritability of the Severity of Diabetic Retinopathy: The FIND-Eye Study

Por Arar, Nedal H., Freedman, Barry I., Adler, Sharon G., Iyengar, Sudha K., Chew, Emily Y., Davis, Mathew D., Satko, Scott G., Bowden, Donald W., Duggirala, Ravi, Elston, Robert C., Guo, Xiuxing, Hanson, Robert L., Igo, Robert P., Ipp, Eli, Kimmel, Paul L., Knowler, William C., Molineros, Julio, Nelson, Robert G., Pahl, Madeleine V., Quade, Shannon R. E., Rasooly, Rebekah S., Rotter, Jerome I., Saad, Mohammed F., Scavini, Marina, Schelling, Jeffrey R., Sedor, John R., Shah, Vallabh O., Zager, Philip G., Abboud, Hanna E.
Publicado em 2008

Genome-wide linkage scans for type 2 diabetes mellitus in four ethnically diverse populations; significant evidence for linkage on chromosome 4q in African Americans: the Family In...

Por Malhotra, Alka, Igo, Robert P., Thameem, Farook, Kao, W.H. Linda, Abboud, Hanna E., Adler, Sharon G., Arar, Nedal H., Bowden, Donald W., Duggirala, Ravindranath, Freedman, Barry I., Goddard, Katrina A.B., Ipp, Eli, Iyengar, Sudha K., Kimmel, Paul L., Knowler, William C., Kohn, Orly, Leehey, David, Meoni, Lucy A., Nelson, Robert G., Nicholas, Susanne B., Parekh, Rulan S., Rich, Stephen S., Chen, Yii-Der I., Saad, Mohammed F., Scavini, Marina, Schelling, Jeffrey R., Sedor, John R., Shah, Vallabh O., Taylor, Kent D., Thornley-Brown, Denyse, Zager, Philip G., Horvath, Amanda, Hanson, Robert L.
Publicado em 2009

Genomewide Linkage Scan for Diabetic Renal Failure and Albuminuria: The FIND Study

Por Igo, Robert P., Iyengar, Sudha K., Nicholas, Susanne B., Goddard, Katrina A.B., Langefeld, Carl D., Hanson, Robert L., Duggirala, Ravindranath, Divers, Jasmin, Abboud, Hanna, Adler, Sharon G., Arar, Nedal H., Horvath, Amanda, Elston, Robert C., Bowden, Donald W., Guo, Xiuqing, Ipp, Eli, Kao, W.H. Linda, Kimmel, Paul L., Knowler, William C., Meoni, Lucy A., Molineros, Julio, Nelson, Robert G., Pahl, Madeline V., Parekh, Rulan S., Rasooly, Rebekah S., Schelling, Jeffrey R., Shah, Vallabh O., Smith, Michael W., Winkler, Cheryl A., Zager, Philip G., Sedor, John R., Freedman, Barry I.
Publicado em 2011