Bilaketaren emaitzak - Malhotra, Alka
- Erakusten 1 - 17 emaitzak -- 17
-
1
-
2
-
3
Analysis of high-density single-nucleotide polymorphism data: three novel methods that control for linkage disequilibrium between markers in a linkage analysis nork Allen-Brady, Kristina, Horne, Benjamin D, Malhotra, Alka, Teerlink, Craig, Camp, Nicola J, Thomas, Alun
Argitaratua 2007Text -
4
-
5
-
6
How does a Social and Behavioral Change Communication Intervention Predict Menstrual Health and Hygiene Management: A Cross-Sectional Study nork Ramaiya, Astha, Malhotra, Alka, Cronin, Carmen, Stevens, Sarah, Kostizak, Kelli, Sharma, Animesh, Nagar, Shailesh, Sood, Suruchi
Argitaratua 2019Text -
7
-
8
-
9
Identity-by-Descent Mapping Identifies Major Locus for Serum Triglycerides in Amerindians Largely Explained by an APOC3 Founder Mutation nork Hsueh, Wen-Chi, Nair, Anup K., Kobes, Sayuko, Chen, Peng, Göring, Harald H. H., Pollin, Toni I., Malhotra, Alka, Knowler, William C., Baier, Leslie J., Hanson, Robert L.
Argitaratua 2017Text -
10
MAP2K3 is associated with body mass index in American Indians and Caucasians and may mediate hypothalamic inflammation nork Bian, Li, Traurig, Michael, Hanson, Robert L., Marinelarena, Alejandra, Kobes, Sayuko, Muller, Yunhua L., Malhotra, Alka, Huang, Ke, Perez, Jessica, Gale, Alex, Knowler, William C., Bogardus, Clifton, Baier, Leslie J.
Argitaratua 2013Text -
11
Expanding the Phenotype of TUBB2A-Related Tubulinopathy: Three Cases of a Novel, Heterozygous TUBB2A Pathogenic Variant p.Gly98Arg nork Schmidt, Lindsey, Wain, Karen E., Hajek, Catherine, Estrada-Veras, Juvianee I., Guillen Sacoto, Maria J., Wentzensen, Ingrid M., Malhotra, Alka, Clause, Amanda, Perry, Denise, Moreno-De-Luca, Andres, Bell, Megan
Argitaratua 2021Text -
12
Evidence for a Role of LPGAT1 in Influencing BMI and Percent Body Fat in Native Americans nork Traurig, Michael T, Orczewska, Julieanna I, Ortiz, Daniel J, Bian, Li, Marinelarena, Alejandra M, Kobes, Sayuko, Malhotra, Alka, Hanson, Robert L, Mason, Clint C, Knowler, William C, Bogardus, Clifton, Baier, Leslie J
Argitaratua 2013Text -
13
De Novo ATP1A1 Variants in an Early-Onset Complex Neurodevelopmental Syndrome nork Dohrn, Maike F., Rebelo, Adriana P., Srivastava, Siddharth, Cappuccio, Gerarda, Smigiel, Robert, Malhotra, Alka, Basel, Donald, van de Laar, Ingrid, Neuteboom, Rinze Frederik, Aarts-Tesselaar, Coranne, Mahida, Sonal, Brunetti-Pierri, Nicola, Taft, Ryan J., Züchner, Stephan
Argitaratua 2022Text -
14
Phenotypic and imaging spectrum associated with WDR45 nork Adang, Laura A., Pizzino, Amy, Malhotra, Alka, Dubbs, Holly, Williams, Catherine, Sherbini, Omar, Anttonen, Anna-Kaisa, Lesca, Gaetan, Linnankivi, Tarja, Laurencin, Chloé, Milh, Matthieu, Perrine, Charles, Schaaf, Christian P., Poulat, Anne-Lise, Ville, Dorothee, Hagelstrom, Tanner, Perry, Denise L., Taft, Ryan J., Goldstein, Amy, Vossough, Arastoo, Helbig, Ingo, Vanderver, Adeline
Argitaratua 2020Text -
15
Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease nork Gross, Andrew M., Ajay, Subramanian S., Rajan, Vani, Brown, Carolyn, Bluske, Krista, Burns, Nicole J., Chawla, Aditi, Coffey, Alison J., Malhotra, Alka, Scocchia, Alicia, Thorpe, Erin, Dzidic, Natasa, Hovanes, Karine, Sahoo, Trilochan, Dolzhenko, Egor, Lajoie, Bryan, Khouzam, Amirah, Chowdhury, Shimul, Belmont, John, Roller, Eric, Ivakhno, Sergii, Tanner, Stephen, McEachern, Julia, Hambuch, Tina, Eberle, Michael, Hagelstrom, R. Tanner, Bentley, David R., Perry, Denise L., Taft, Ryan J.
Argitaratua 2018Text -
16
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... nork 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.
Argitaratua 2009Text -
17
Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND) nork Iyengar, Sudha K., Sedor, John R., Freedman, Barry I., Kao, W. H. Linda, Kretzler, Matthias, Keller, Benjamin J., Abboud, Hanna E., Adler, Sharon G., Best, Lyle G., Bowden, Donald W., Burlock, Allison, Chen, Yii-Der Ida, Cole, Shelley A., Comeau, Mary E., Curtis, Jeffrey M., Divers, Jasmin, Drechsler, Christiane, Duggirala, Ravi, Elston, Robert C., Guo, Xiuqing, Huang, Huateng, Hoffmann, Michael Marcus, Howard, Barbara V., Ipp, Eli, Kimmel, Paul L., Klag, Michael J., Knowler, William C., Kohn, Orly F., Leak, Tennille S., Leehey, David J., Li, Man, Malhotra, Alka, März, Winfried, Nair, Viji, Nelson, Robert G., Nicholas, Susanne B., O’Brien, Stephen J., Pahl, Madeleine V., Parekh, Rulan S., Pezzolesi, Marcus G., Rasooly, Rebekah S., Rotimi, Charles N., Rotter, Jerome I., Schelling, Jeffrey R., Seldin, Michael F., Shah, Vallabh O., Smiles, Adam M., Smith, Michael W., Taylor, Kent D., Thameem, Farook, Thornley-Brown, Denyse P., Truitt, Barbara J., Wanner, Christoph, Weil, E. Jennifer, Winkler, Cheryl A., Zager, Philip G., Igo, Robert P., Hanson, Robert L., Langefeld, Carl D.
Argitaratua 2015Text