Risultati della ricerca - Cutiongco-de la Paz, Eva Maria

AB022. Harnessing big data to transform clinical care of cardiovascular diseases di Cutiongco-de la Paz, Eva Maria

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Genetics and genomic medicine in the Philippines di Padilla, Carmencita D., Cutiongco‐de la Paz, Eva Maria

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Phenotypic characterization of the novel, non-hotspot oncogenic KRAS mutants E31D and E63K di Angeles, Arlou Kristina J., Yu, Ryan Timothy D., Cutiongco-De La Paz, Eva Maria, Garcia, Reynaldo L.

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The Novel Phosphatase Domain Mutations Q171R and Y65S Switch PTEN from Tumor Suppressor to Oncogene di Garrido, Jose Antonio Ma. G., Alcantara, Krizelle Mae M., Danac, Joshua Miguel C., Serrano, Fidel Emmanuel C., Cutiongco-de la Paz, Eva Maria, Garcia, Reynaldo L.

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Non-Redundant and Overlapping Oncogenic Readouts of Non-Canonical and Novel Colorectal Cancer KRAS and NRAS Mutants di Alcantara, Krizelle Mae M., Malapit, Joshua Reginald P., Yu, Ryan Timothy D., Garrido, Jose Antonio Ma. G., Rigor, John Paul T., Angeles, Arlou Kristina J., Cutiongco-de la Paz, Eva Maria, Garcia, Reynaldo L.

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The SLC26A4 c.706C>G (p.Leu236Val) variant is a frequent cause of hearing impairment in Filipino cochlear implantees di Chiong, Charlotte M., Reyes-Quintos, Ma. Rina T., Yarza, Talitha Karisse L., Tobias-Grasso, Celina Ann M., Acharya, Anushree, Leal, Suzanne M., Mohlke, Karen L., Mayol, Nanette L., Cutiongco-de la Paz, Eva Maria, Santos-Cortez, Regie Lyn P.

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Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees di Truong, Brittany T., Yarza, Talitha Karisse L., Roberts, Tori Bootpetch, Roberts, Susannah, Xu, Jonathan, Steritz, Matthew J., Tobias-Grasso, Celina Ann M., Azamian, Mahshid, Lalani, Seema R., Mohlke, Karen L., Lee, Nanette R., Cutiongco-de la Paz, Eva Maria, Reyes-Quintos, Maria Rina T., Santos-Cortez, Regie Lyn P., Chiong, Charlotte M.

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Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone Anomalies di Santos-Cortez, Regie Lyn P., Yarza, Talitha Karisse L., Bootpetch, Tori C., Tantoco, Ma. Leah C., Mohlke, Karen L., Cruz, Teresa Luisa G., Chiong Perez, Mary Ellen, Chan, Abner L., Lee, Nanette R., Tobias-Grasso, Celina Ann M., Reyes-Quintos, Maria Rina T., Cutiongco-de la Paz, Eva Maria, Chiong, Charlotte M.

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Genetic and Environmental Determinants of Otitis Media in an Indigenous Filipino Population di Santos-Cortez, Regie Lyn P., Reyes-Quintos, Ma. Rina T., Tantoco, Ma. Leah C., Abbe, Izoduwa, Llanes, Erasmo Gonzalo d.V., Ajami, Nadim J., Hutchinson, Diane S., Petrosino, Joseph F., Padilla, Carmencita D., Villarta, Romeo L., Gloria-Cruz, Teresa Luisa, Chan, Abner L., Cutiongco-de la Paz, Eva Maria, Chiong, Charlotte M., Leal, Suzanne M., Abes, Generoso T.

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Middle ear microbiome differences in indigenous Filipinos with chronic otitis media due to a duplication in the A2ML1 gene di Santos-Cortez, Regie Lyn P., Hutchinson, Diane S., Ajami, Nadim J., Reyes-Quintos, Ma. Rina T., Tantoco, Ma. Leah C., Labra, Patrick John, Lagrana, Sheryl Mae, Pedro, Melquiadesa, Llanes, Erasmo Gonzalo d. V., Gloria-Cruz, Teresa Luisa, Chan, Abner L., Cutiongco-de la Paz, Eva Maria, Belmont, John W., Chonmaitree, Tasnee, Abes, Generoso T., Petrosino, Joseph F., Leal, Suzanne M., Chiong, Charlotte M.

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The rs1458038 variant near FGF5 is associated with poor response to calcium channel blockers among Filipinos di Punzalan, Felix Eduardo R., Cutiongco – de la Paz, Eva Maria C., Nevado, Jose Jr. B., Magno, Jose Donato A., Ona, Deborah Ignacia D., Aman, Aimee Yvonne Criselle L., Tiongson, Marc Denver A., Llanes, Elmer Jasper B., Reganit, Paul Ferdinand M., Tiongco, Richard Henry P., Santos, Lourdes Ella G., Aherrera, Jaime Alfonso M., Abrahan, Lauro L., Agustin, Charlene F., Bejarin, Adrian John P., Sy, Rody G.

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Rare A2ML1 variants confer susceptibility to otitis media di Santos-Cortez, Regie Lyn P., Chiong, Charlotte M., Reyes-Quintos, Ma. Rina T., Tantoco, Ma. Leah C., Wang, Xin, Acharya, Anushree, Abbe, Izoduwa, Giese, Arnaud P., Smith, Joshua D., Allen, E. Kaitlynn, Li, Biao, Cutiongco-de la Paz, Eva Maria, Garcia, Marieflor Cristy, Llanes, Erasmo Gonzalo D.V., Labra, Patrick John, Gloria-Cruz, Teresa Luisa I., Chan, Abner L., Wang, Gao T., Daly, Kathleen A., Shendure, Jay, Bamshad, Michael J., Nickerson, Deborah A., Patel, Janak A., Riazuddin, Saima, Sale, Michele M., Chonmaitree, Tasnee, Ahmed, Zubair M., Abes, Generoso T., Leal, Suzanne M.

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Variants of SLC2A10 may be Linked to Poor Response to Metformin di Paz-Pacheco, Elizabeth, Nevado, Jose B, Cutiongco-de la Paz, Eva Maria C, Jasul, Gabriel V, Aman, Aimee Yvonne Criselle L, Ribaya, Elizabeth Laurize A, Francisco, Mark David G, Guanzon, Ma Luz Vicenta V, Uyking-Naranjo, May L, Añonuevo-Cruz, Ma Cecille S, Maningat, Maria Patricia Deanna D, Jaring, Cristina V, Nacpil-Dominguez, Paulette D, Pala-Mohamad, Aniza B, Canto, Abigail U, Quisumbing, John Paul M, Lat, Annabelle Marie M, Bernardo, Diane Carla C, Mansibang, Noemie Marie M, Calpito, Karell Jo Angelique C, Ribaya, Vincent Sean D, Ferrer, Julius Patrick Y, Biwang, Jessica H, Melegrito, Jodelyn B, Deguit, Christian Deo T, Panerio, Carlos Emmanuel G

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Detection and Genome Sequencing of SARS-CoV-2 Variants Belonging to the B.1.1.7 Lineage in the Philippines di Tablizo, Francis A., Saloma, Cynthia P., Castro, Marc Jerrone R., Kim, Kenneth M., Yangzon, Maria Sofia L., Lapid, Carlo M., Maralit, Benedict A., Ayes, Marc Edsel C., Yap, Jan Michael C., Llames, Jo-Hannah S., Araiza, Shiela Mae M., Punayan, Kris P., Asin, Irish Coleen A., Tambaoan, Candice Francheska B., Chong, Asia Louisa U., Padilla, Karol Sophia Agape R., Cruz, Rianna Patricia S., Morado, El King D., Dizon, Joshua Gregor A., Cutiongco-de la Paz, Eva Maria, de Guzman, Alethea R., Hao, Razel Nikka M., Zamora, Arianne A., Pacial, Devon Ray, Magalang, Juan Antonio R., Alejandria, Marissa, Carlos, Celia, Ong-Lim, Anna, Salvaña, Edsel Maurice, Wong, John Q., Montoya, Jaime C., Singh-Vergeire, Maria Rosario

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OTITIS MEDIA SUSCEPTIBILITY AND SHIFTS IN THE HEAD AND NECK MICROBIOME DUE TO SPINK5 VARIANTS di Frank, Daniel N., Giese, Arnaud P.J., Hafrén, Lena, Bootpetch, Tori C., Yarza, Talitha Karisse L., Steritz, Matthew J., Pedro, Melquiadesa, Labra, Patrick John, Daly, Kathleen A., Tantoco, Ma. Leah C., Szeremeta, Wasyl, Reyes-Quintos, Maria Rina T., Ahankoob, Niaz, Llanes, Erasmo Gonzalo d.V., Pine, Harold S., Yousaf, Sairah, Ir, Diana, Einarsdottir, Elisabet, de la Cruz, Rhodieleen Anne R., Lee, Nanette R., Nonato, Rachelle Marie A., Robertson, Charles E., Ong, Kimberly Mae C., Magno, Jose Pedrito M., Chiong, Alessandra Nadine E., Espiritu-Chiong, Ma. Carmina, Agustin, Ma. Luz San, Cruz, Teresa Luisa G., Abes, Generoso T., Bamshad, Michael J., Cutiongco-de la Paz, Eva Maria, Kere, Juha, Nickerson, Deborah A., Mohlke, Karen L., Riazuddin, Saima, Chan, Abner L., Mattila, Petri S., Leal, Suzanne M., Ryan, Allen F., Ahmed, Zubair M., Chonmaitree, Tasnee, Sale, Michele M., Chiong, Charlotte M., Santos-Cortez, Regie Lyn P.

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A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13 di Leslie, Elizabeth J., Carlson, Jenna C., Shaffer, John R., Feingold, Eleanor, Wehby, George, Laurie, Cecelia A., Jain, Deepti, Laurie, Cathy C., Doheny, Kimberly F., McHenry, Toby, Resick, Judith, Sanchez, Carla, Jacobs, Jennifer, Emanuele, Beth, Vieira, Alexandre R., Neiswanger, Katherine, Lidral, Andrew C., Valencia-Ramirez, Luz Consuelo, Lopez-Palacio, Ana Maria, Valencia, Dora Rivera, Arcos-Burgos, Mauricio, Czeizel, Andrew E., Field, L. Leigh, Padilla, Carmencita D., Cutiongco-de la Paz, Eva Maria, C., Deleyiannis, Frederic, Christensen, Kaare, Munger, Ronald G., Lie, Rolv T., Wilcox, Allen, Romitti, Paul A., Castilla, Eduardo E., Mereb, Juan C., Poletta, Fernando A., Orioli, Iêda M., Carvalho, Flavia M., Hecht, Jacqueline T., Blanton, Susan H., Buxó, Carmen J., Butali, Azeez, Mossey, Peter A., Adeyemo, Wasiu L., James, Olutayo, Braimah, Ramat O., Aregbesola, Babatunde S., Eshete, Mekonen A., Abate, Fikre, Koruyucu, Mine, Seymen, Figen, Ma, Lian, de Salamanca, Javier Enríquez, Weinberg, Seth M., Moreno, Lina, Murray, Jeffrey C., Marazita, Mary L.

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A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3 di Leslie, Elizabeth J., Liu, Huan, Carlson, Jenna C., Shaffer, John R., Feingold, Eleanor, Wehby, George, Laurie, Cecelia A., Jain, Deepti, Laurie, Cathy C., Doheny, Kimberly F., McHenry, Toby, Resick, Judith, Sanchez, Carla, Jacobs, Jennifer, Emanuele, Beth, Vieira, Alexandre R., Neiswanger, Katherine, Standley, Jennifer, Czeizel, Andrew E., Deleyiannis, Frederic, Christensen, Kaare, Munger, Ronald G., Lie, Rolv T., Wilcox, Allen, Romitti, Paul A., Field, L. Leigh, Padilla, Carmencita D., Cutiongco-de la Paz, Eva Maria C., Lidral, Andrew C., Valencia-Ramirez, Luz Consuelo, Lopez-Palacio, Ana Maria, Valencia, Dora Rivera, Arcos-Burgos, Mauricio, Castilla, Eduardo E., Mereb, Juan C., Poletta, Fernando A., Orioli, Iêda M., Carvalho, Flavia M., Hecht, Jacqueline T., Blanton, Susan H., Buxó, Carmen J., Butali, Azeez, Mossey, Peter A., Adeyemo, Wasiu L., James, Olutayo, Braimah, Ramat O., Aregbesola, Babatunde S., Eshete, Mekonen A., Deribew, Milliard, Koruyucu, Mine, Seymen, Figen, Ma, Lian, de Salamanca, Javier Enríquez, Weinberg, Seth M., Moreno, Lina, Cornell, Robert A., Murray, Jeffrey C., Marazita, Mary L.

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A2ML1 and otitis media: novel variants, differential expression and relevant pathways di Larson, Eric D., Magno, Jose Pedrito M., Steritz, Matthew J., Llanes, Erasmo Gonzalo d.V., Cardwell, Jonathan, Pedro, Melquiadesa, Roberts, Tori Bootpetch, Einarsdottir, Elisabet, Rosanes, Rose Anne Q., Greenlee, Christopher, Santos, Rachel Ann P., Yousaf, Ayesha, Streubel, Sven-Olrik, Santos, Aileen Trinidad R., Ruiz, Amanda G., Lagrana-Villagracia, Sheryl Mae, Ray, Dylan, Yarza, Talitha Karisse L., Scholes, Melissa A., Anderson, Catherine B., Acharya, Anushree, Gubbels, Samuel P., Bamshad, Michael J., Cass, Stephen P., Lee, Nanette R., Shaikh, Rehan S., Nickerson, Deborah A., Mohlke, Karen L., Prager, Jeremy D., Cruz, Teresa Luisa G., Yoon, Patricia J., Abes, Generoso T., Schwartz, David A., Chan, Abner L., Wine, Todd M., Cutiongco-de la Paz, Eva Maria, Friedman, Norman, Kechris, Katerina, Kere, Juha, Leal, Suzanne M., Yang, Ivana V., Patel, Janak A., Tantoco, Ma. Leah C., Riazuddin, Saima, Chan, Kenny H., Mattila, Petri S., Reyes-Quintos, Maria Rina T., Ahmed, Zubair M., Jenkins, Herman A., Chonmaitree, Tasnee, Hafrén, Lena, Chiong, Charlotte M., Santos-Cortez, Regie Lyn P.

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FUT2 Variants Confer Susceptibility to Familial Otitis Media di Santos-Cortez, Regie Lyn P., Chiong, Charlotte M., Frank, Daniel N., Ryan, Allen F., Giese, Arnaud P.J., Bootpetch Roberts, Tori, Daly, Kathleen A., Steritz, Matthew J., Szeremeta, Wasyl, Pedro, Melquiadesa, Pine, Harold, Yarza, Talitha Karisse L., Scholes, Melissa A., Llanes, Erasmo Gonzalo d.V., Yousaf, Saira, Friedman, Norman, Tantoco, Ma. Leah C., Wine, Todd M., Labra, Patrick John, Benoit, Jeanne, Ruiz, Amanda G., de la Cruz, Rhodieleen Anne R., Greenlee, Christopher, Yousaf, Ayesha, Cardwell, Jonathan, Nonato, Rachelle Marie A., Ray, Dylan, Ong, Kimberly Mae C., So, Edward, Robertson, Charles E., Dinwiddie, Jordyn, Lagrana-Villagracia, Sheryl Mae, Gubbels, Samuel P., Shaikh, Rehan S., Cass, Stephen P., Einarsdottir, Elisabet, Lee, Nanette R., Schwartz, David A., Gloria-Cruz, Teresa Luisa I., Bamshad, Michael J., Yang, Ivana V., Kere, Juha, Abes, Generoso T., Prager, Jeremy D., Riazuddin, Saima, Chan, Abner L., Yoon, Patricia J., Nickerson, Deborah A., Cutiongco-de la Paz, Eva Maria, Streubel, Sven-Olrik, Reyes-Quintos, Maria Rina T., Jenkins, Herman A., Mattila, Petri, Chan, Kenny H., Mohlke, Karen L., Leal, Suzanne M., Hafrén, Lena, Chonmaitree, Tasnee, Sale, Michele M., Ahmed, Zubair M.

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