Linkage analysis of adult height with parent-of-origin effects in the Framingham Heart Study

由 Mukhopadhyay, Nandita, Weeks, Daniel E
出版 2003

Two-dimensional linkage analyses of rheumatoid arthritis

由 Mukhopadhyay, Nandita, Halder, Indrani, Bhattacharjee, Samsiddhi, Weeks, Daniel E
出版 2007

Mega2: validated data-reformatting for linkage and association analyses

由 Baron, Robert V, Kollar, Charles, Mukhopadhyay, Nandita, Weeks, Daniel E
發表在 Source Code Biol Med (2014)

Analysis of alcohol dependence phenotype in the COGA families using covariates to detect linkage

由 Reck, Brian H, Mukhopadhyay, Nandita, Tsai, Hui-Ju, Weeks, Daniel E
出版 2005

A Pipeline for Classifying Relationships Using Dense SNP/SNV Data and Putative Pedigree Information

由 Zeng, Zhen, Weeks, Daniel E, Chen, Wei, Mukhopadhyay, Nandita, Feingold, Eleanor
發表在 Genet Epidemiol (2015)

Identifying genetic risk loci for diabetic complications and showing evidence for heterogeneity of type 1 diabetes based on complications risk

由 Mukhopadhyay, Nandita, Noble, Janelle A., Govil, Manika, Marazita, Mary L., Greenberg, David A.
發表在 PLoS One (2018)

Robust Score Statistics for QTL Linkage Analysis

由 Bhattacharjee, Samsiddhi, Kuo, Chia-Ling, Mukhopadhyay, Nandita, Brock, Guy N., Weeks, Daniel E., Feingold, Eleanor
出版 2008

Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21

由 Middlebrooks, Candace D., Mukhopadhyay, Nandita, Tinker, Stuart W., Allen, Emily Graves, Bean, Lora J. H., Begum, Ferdouse, Chowdhury, Reshmi, Cheung, Vivian, Doheny, Kimberly, Adams, Marcia, Feingold, Eleanor, Sherman, Stephanie L.
出版 2014

Individuals with nonsyndromic orofacial clefts have increased asymmetry of fingerprint patterns

由 Neiswanger, Katherine, Mukhopadhyay, Nandita, Rajagopalan, Shwetha, Leslie, Elizabeth J., Sanchez, Carla A., Hecht, Jacqueline T., Orioli, Iêda M., Poletta, Fernando A., de Salamanca, Javier Enríquez, Weinberg, Seth M., Marazita, Mary L.
發表在 PLoS One (2020)

Novel caries loci in children and adults implicated by genome-wide analysis of families

由 Govil, Manika, Mukhopadhyay, Nandita, Weeks, Daniel E., Feingold, Eleanor, Shaffer, John R., Levy, Steven M., Vieira, Alexandre R., Slayton, Rebecca L., McNeil, Daniel W., Weyant, Robert J., Crout, Richard J., Marazita, Mary L.
發表在 BMC Oral Health (2018)

Cleft lip/palate and educational attainment: cause, consequence or correlation? A Mendelian randomization study

由 Dardani, Christina, Howe, Laurence J, Mukhopadhyay, Nandita, Stergiakouli, Evie, Wren, Yvonne, Humphries, Kerry, Davies, Amy, Ho, Karen, Weinberg, Seth M, Marazita, Mary L, Mangold, Elisabeth, Ludwig, Kerstin U, Relton, Caroline L, Davey Smith, George, Lewis, Sarah J, Sandy, Jonathan, Davies, Neil M, Sharp, Gemma C
發表在 Int J Epidemiol (2020)

Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21

由 Mukhopadhyay, Nandita, Bishop, Madison, Mortillo, Michael, Chopra, Pankaj, Hetmanski, Jacqueline B., Taub, Margaret A., Moreno, Lina M., Valencia-Ramirez, Luz Consuelo, Restrepo, Claudia, Wehby, George L., Hecht, Jacqueline T., Deleyiannis, Frederic, Butali, Azeez, Weinberg, Seth M., Beaty, Terri H., Murray, Jeffrey C., Leslie, Elizabeth J., Feingold, Eleanor, Marazita, Mary L.
發表在 Hum Genet (2019)

Genome-Wide Association Study (GWAS) of dental caries in diverse populations

由 Alotaibi, Rasha N., Howe, Brian J., Chernus, Jonathan M., Mukhopadhyay, Nandita, Sanchez, Carla, Deleyiannis, Frederic W. B., Neiswanger, Katherine, Padilla, Carmencita, Poletta, Fernando A., Orioli, Ieda M., Buxó, Carmen J., Hecht, Jacqueline T., Wehby, George L., Long, Ross E., Vieira, Alexandre R., Weinberg, Seth M., Shaffer, John R., Moreno Uribe, Lina M., Marazita, Mary L.
發表在 BMC Oral Health (2021)

Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions

由 Mukhopadhyay, Nandita, Feingold, Eleanor, Moreno-Uribe, Lina, Wehby, George, Valencia-Ramirez, Luz Consuelo, Muñeton, Claudia P. Restrepo, Padilla, Carmencita, Deleyiannis, Frederic, Christensen, Kaare, Poletta, Fernando A., Orioli, Ieda M., Hecht, Jacqueline T., Buxó, Carmen J., Butali, Azeez, Adeyemo, Wasiu L., Vieira, Alexandre R., Shaffer, John R., Murray, Jeffrey C., Weinberg, Seth M., Leslie, Elizabeth J., Marazita, Mary L.
發表在 Front Cell Dev Biol (2021)

Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios

由 Bishop, Madison R., Diaz Perez, Kimberly K., Sun, Miranda, Ho, Samantha, Chopra, Pankaj, Mukhopadhyay, Nandita, Hetmanski, Jacqueline B., Taub, Margaret A., Moreno-Uribe, Lina M., Valencia-Ramirez, Luz Consuelo, Restrepo Muñeton, Claudia P., Wehby, George, Hecht, Jacqueline T., Deleyiannis, Frederic, Weinberg, Seth M., Wu-Chou, Yah Huei, Chen, Philip K., Brand, Harrison, Epstein, Michael P., Ruczinski, Ingo, Murray, Jeffrey C., Beaty, Terri H., Feingold, Eleanor, Lipinski, Robert J., Cutler, David J., Marazita, Mary L., Leslie, Elizabeth J.
發表在 Am J Hum Genet (2020)