Suchergebnisse - Malhotra, Alka
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Analysis of high-density single-nucleotide polymorphism data: three novel methods that control for linkage disequilibrium between markers in a linkage analysis von Allen-Brady, Kristina, Horne, Benjamin D, Malhotra, Alka, Teerlink, Craig, Camp, Nicola J, Thomas, Alun
Veröffentlicht 2007Text -
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How does a Social and Behavioral Change Communication Intervention Predict Menstrual Health and Hygiene Management: A Cross-Sectional Study von Ramaiya, Astha, Malhotra, Alka, Cronin, Carmen, Stevens, Sarah, Kostizak, Kelli, Sharma, Animesh, Nagar, Shailesh, Sood, Suruchi
Veröffentlicht 2019Text -
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Identity-by-Descent Mapping Identifies Major Locus for Serum Triglycerides in Amerindians Largely Explained by an APOC3 Founder Mutation von 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.
Veröffentlicht 2017Text -
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MAP2K3 is associated with body mass index in American Indians and Caucasians and may mediate hypothalamic inflammation von 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.
Veröffentlicht 2013Text -
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Expanding the Phenotype of TUBB2A-Related Tubulinopathy: Three Cases of a Novel, Heterozygous TUBB2A Pathogenic Variant p.Gly98Arg von 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
Veröffentlicht 2021Text -
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Evidence for a Role of LPGAT1 in Influencing BMI and Percent Body Fat in Native Americans von 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
Veröffentlicht 2013Text -
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De Novo ATP1A1 Variants in an Early-Onset Complex Neurodevelopmental Syndrome von 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
Veröffentlicht 2022Text -
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Phenotypic and imaging spectrum associated with WDR45 von 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
Veröffentlicht 2020Text -
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Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease von 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.
Veröffentlicht 2018Text -
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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... von 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.
Veröffentlicht 2009Text -
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Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND) von 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.
Veröffentlicht 2015Text