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Eva Maria Cutiongco-de la Paz
Researcher at University of the Philippines Manila
Publications - 51
Citations - 1239
Eva Maria Cutiongco-de la Paz is an academic researcher from University of the Philippines Manila. The author has contributed to research in topics: Otitis & Medicine. The author has an hindex of 11, co-authored 45 publications receiving 1033 citations. Previous affiliations of Eva Maria Cutiongco-de la Paz include University of the Philippines Diliman & Philippines Department of Health.
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Journal ArticleDOI
Mapping human genetic diversity in Asia
Mahmood Ameen Abdulla,Ikhlak Ahmed,Anunchai Assawamakin,Anunchai Assawamakin,Jong Bhak,Samir K. Brahmachari,Gayvelline C. Calacal,Amit Kumar Chaurasia,Chien-Hsiun Chen,Jieming Chen,Yuan-Tsong Chen,Jiayou Chu,Eva Maria Cutiongco-de la Paz,Maria Corazon A. De Ungria,Frederick C. Delfin,Juli Edo,Suthat Fuchareon,Ho Ghang,Takashi Gojobori,Junsong Han,Sheng Feng Ho,Boon Peng Hoh,Wei Huang,Hidetoshi Inoko,Pankaj Jha,Timothy A. Jinam,Li Jin,Jongsun Jung,Daoroong Kangwanpong,Jatupol Kampuansai,Giulia C. Kennedy,Preeti Khurana,Hyung Lae Kim,Kwangjoong Kim,Sangsoo Kim,Woo Yeon Kim,Kuchan Kimm,Ryosuke Kimura,Tomohiro Koike,Supasak Kulawonganunchai,Vikrant Kumar,Poh San Lai,Jong-Young Lee,Sunghoon Lee,Edison T. Liu,Partha P. Majumder,Kiran Kumar Mandapati,Sangkot Marzuki,Wayne Mitchell,Wayne Mitchell,Mitali Mukerji,Kenji Naritomi,Chumpol Ngamphiw,Norio Niikawa,Nao Nishida,Bermseok Oh,Sangho Oh,Jun Ohashi,Akira Oka,Rick Twee-Hee Ong,Carmencita Padilla,Prasit Palittapongarnpim,Henry B. Perdigon,Maude E. Phipps,Maude E. Phipps,Eileen Png,Yoshiyuki Sakaki,Jazelyn M. Salvador,Yuliana Sandraling,Vinod Scaria,Mark Seielstad,Mohd Ros Sidek,Amit Sinha,Metawee Srikummool,Herawati Sudoyo,Sumio Sugano,Helena Suryadi,Yoshiyuki Suzuki,Kristina A. Tabbada,Adrian Tan,Katsushi Tokunaga,Sissades Tongsima,Lilian P. Villamor,Eric Wang,Ying Wang,Haifeng Wang,Jer-Yuarn Wu,Huasheng Xiao,Shuhua Xu,Jin Ok Yang,Yin Yao Shugart,Hyang Sook Yoo,Wentao Yuan,Guoping Zhao,Bin Alwi Zilfalil +94 more
TL;DR: The results suggest that there may have been a single major migration of people into Asia and a subsequent south-to-north migration across the continent, and that genetic ancestry is strongly correlated with linguistic affiliations as well as geography.
Journal ArticleDOI
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
Elizabeth J. Leslie,Jenna C. Carlson,John R. Shaffer,Eleanor Feingold,George L. Wehby,Cecelia A. Laurie,Deepti Jain,Cathy C. Laurie,Kimberly F. Doheny,Toby Goldstein McHenry,Judith M. Resick,Carla A. Sanchez,Jennifer Jacobs,Beth Emanuele,Alexandre R. Vieira,Katherine Neiswanger,Andrew C. Lidral,Luz Consuelo Valencia-Ramirez,Ana Maria Lopez-Palacio,Dora Rivera Valencia,Mauricio Arcos-Burgos,Andrew E. Czeizel,L. Leigh Field,Carmencita Padilla,Eva Maria Cutiongco-de la Paz,Frederic W.-B. Deleyiannis,Kaare Christensen,Ronald G. Munger,Rolv T. Lie,Allen J. Wilcox,Paul A. Romitti,Eduardo E. Castilla,Juan C. Mereb,Fernando A. Poletta,Iêda M. Orioli,Flávia Martinez de Carvalho,Jacqueline T. Hecht,Susan H. Blanton,Carmen J. Buxó,Azeez Butali,Peter A. Mossey,Wasiu Lanre Adeyemo,Olutayo James,Ramat Oyebunmi Braimah,Babatunde S. Aregbesola,Mekonen Eshete,Fikre Abate,Mine Koruyucu,Figen Seymen,Lian Ma,Javier Enríquez de Salamanca,Seth M. Weinberg,Lina M. Moreno,Jeffrey C. Murray,Mary L. Marazita +54 more
TL;DR: A multiethnic genome-wide association study with European, Asian, African and Central and South American ancestry revealed novel CL/P risk loci and suggest new genes involved in craniofacial development, confirming the highly heterogeneous etiology of OFCs.
Journal ArticleDOI
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3
Elizabeth J. Leslie,Huan Liu,Huan Liu,Jenna C. Carlson,John R. Shaffer,Eleanor Feingold,George L. Wehby,Cecelia A. Laurie,Deepti Jain,Cathy C. Laurie,Kimberly F. Doheny,Toby Goldstein McHenry,Judith M. Resick,Carla A. Sanchez,Jennifer Jacobs,Beth Emanuele,Alexandre R. Vieira,Katherine Neiswanger,Jennifer Standley,Andrew E. Czeizel,Frederic W.-B. Deleyiannis,Kaare Christensen,Ronald G. Munger,Rolv T. Lie,Allen J. Wilcox,Paul A. Romitti,L. Leigh Field,Carmencita Padilla,Eva Maria Cutiongco-de la Paz,Eva Maria Cutiongco-de la Paz,Andrew C. Lidral,Luz Consuelo Valencia-Ramirez,Ana Maria Lopez-Palacio,Dora Rivera Valencia,Mauricio Arcos-Burgos,Eduardo E. Castilla,Juan C. Mereb,Fernando A. Poletta,Iêda M. Orioli,Flávia Martinez de Carvalho,Jacqueline T. Hecht,Susan H. Blanton,Carmen J. Buxó,Azeez Butali,Peter A. Mossey,Wasiu Lanre Adeyemo,Olutayo James,Ramat Oyebunmi Braimah,Babatunde S. Aregbesola,Mekonen Eshete,Milliard Deribew,Mine Koruyucu,Figen Seymen,Lian Ma,Javier Enríquez de Salamanca,Seth M. Weinberg,Lina M. Moreno,Robert A. Cornell,Jeffrey C. Murray,Mary L. Marazita +59 more
TL;DR: A genome-wide significant association with a missense variant in GRHL3 is discovered and it is concluded that this mutation is an etiologic variant for nonsyndromic CP and is one of few functional variants identified to date for nonsYNDromic orofacial clefting.
Journal ArticleDOI
New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3).
Aloysius Domingo,Ana Westenberger,Lillian V. Lee,Ingrid Braenne,Tian Liu,Inga Vater,Raymond L. Rosales,Roland Dominic G. Jamora,Paul Matthew D. Pasco,Eva Maria Cutiongco-de la Paz,Karen Freimann,Thomas G. P. M. Schmidt,Dirk Dressler,Frank J. Kaiser,Lars Bertram,Jeanette Erdmann,Katja Lohmann,Christine Klein +17 more
TL;DR: The finding of disease-specific variants occurring in complete linkage disequilibrium raises new insights and intriguing questions about the origin of the disease haplotype, the existence of phenocopies and of reduced penetrance, and the causative genetic alteration in XDP.
Journal ArticleDOI
Rare A2ML1 variants confer susceptibility to otitis media
Regie Lyn P. Santos-Cortez,Charlotte M. Chiong,Ma. Rina T. Reyes-Quintos,Ma. Leah C. Tantoco,Xin Wang,Anushree Acharya,Izoduwa Abbe,Arnaud P. J. Giese,Joshua D. Smith,E. Kaitlynn Allen,Biao Li,Eva Maria Cutiongco-de la Paz,Marieflor Cristy M. Garcia,Erasmo Gonzalo D V Llanes,Patrick John Labra,Teresa Luisa I Gloria-Cruz,Abner L. Chan,Gao Wang,Kathleen Daly,Jay Shendure,Michael J. Bamshad,Deborah A. Nickerson,Janak A. Patel,Saima Riazuddin,Michèle M. Sale,Tasnee Chonmaitree,Zubair M. Ahmed,Generoso T. Abes,Suzanne M. Leal +28 more
TL;DR: A duplication variant within the middle ear–specific gene A2ML1 cosegregates with otitis media in an indigenous Filipino pedigree and lies within a founder haplotype that is also shared by 3 otitis-prone European-American and Hispanic-American children but is absent in non-otitis- prone children and >62,000 next-generation sequences.