日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Tracking development assistance for health, 1990-2030: historical trends, recent cuts, and outlook

追踪1990-2030年卫生发展援助:历史趋势、近期削减及展望

Apeagyei, Angela E; Bisignano, Catherine; Elliott, Hans; Hay, Simon I; Lidral-Porter, Brendan; Nam, Seong; Shyong, Carolyn; Tsakalos, Golsum; Zlavog, Bianca S; Barış, Enis; Murray, Christopher J L; Dieleman, Joseph L

Financing health in sub-Saharan Africa 1990-2050: Donor dependence and expected domestic health spending

1990-2050年撒哈拉以南非洲卫生筹资:对捐助方的依赖和预期国内卫生支出

Apeagyei, Angela E; Lidral-Porter, Brendan; Patel, Nishali; Solorio, Juan; Tsakalos, Golsum; Wang, Yifeng; Warriner, Wesley; Wolde, Asrat; Zhao, Yingxi; Dieleman, Joseph L; Nonvignon, Justice

A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature

AMOTL1基因中的一个突变热点定义了一种新的综合征,其特征为唇腭裂、心脏畸形和身材高大

Strong, Alanna; Rao, Soumya; von Hardenberg, Sandra; Li, Dong; Cox, Liza L; Lee, Paul C; Zhang, Li Q; Awotoye, Waheed; Diamond, Tamir; Gold, Jessica; Gooch, Catherine; Gowans, Lord Jephthah Joojo; Hakonarson, Hakon; Hing, Anne; Loomes, Kathleen; Martin, Nicole; Marazita, Mary L; Mononen, Tarja; Piccoli, David; Pfundt, Rolph; Raskin, Salmo; Scherer, Stephen W; Sobriera, Nara; Vaccaro, Courtney; Wang, Xiang; Watson, Deborah; Weksberg, Rosanna; Bhoj, Elizabeth; Murray, Jeffrey C; Lidral, Andrew C; Butali, Azeez; Buckley, Michael F; Roscioli, Tony; Koolen, David A; Seaver, Laurie H; Prows, Cynthia A; Stottmann, Rolf W; Cox, Timothy C

Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans

GDF11基因及其胞外拮抗剂卵泡抑素的突变可能是人类孟德尔遗传性唇腭裂的病因。

Timothy C Cox ,Andrew C Lidral,Jason C McCoy,Huan Liu,Liza L Cox   ,Ying Zhu ,Ryan D Anderson,Lina M Moreno Uribe,Deepti Anand,Mei Deng,Chika T Richter,Nichole L Nidey,Jennifer M Standley,Elizabeth E Blue,Jessica X Chong,Joshua D Smith,Edwin P Kirk ,Hanka Venselaar,Katy N Krahn,Hans van Bokhoven  ,Huiqing Zhou  ,Robert A Cornell,Ian A Glass ,Michael J Bamshad ,Deborah A Nickerson,Jeffrey C Murray,Salil A Lachke,Thomas B Thompson,Michael F Buckley,Tony Roscioli

Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting

识别 1p22 处对非综合征性颌面裂有作用的常见非编码变异

Huan Liu, Elizabeth J Leslie, Jenna C Carlson, Terri H Beaty, Mary L Marazita, Andrew C Lidral, Robert A Cornell

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3

一项针对非综合征型腭裂的全基因组关联研究发现GRHL3基因中存在致病性错义变异

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

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

一项多民族全基因组关联研究在 2p24.2、17q23 和 19q13 上发现了与非综合征性唇裂(伴或不伴腭裂)相关的新基因位点。

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

A single nucleotide polymorphism associated with isolated cleft lip and palate, thyroid cancer and hypothyroidism alters the activity of an oral epithelium and thyroid enhancer near FOXE1

与孤立性唇腭裂、甲状腺癌和甲状腺功能减退症相关的单核苷酸多态性会改变FOXE1附近口腔上皮和甲状腺增强子的活性。

Lidral, Andrew C; Liu, Huan; Bullard, Steven A; Bonde, Greg; Machida, Junichiro; Visel, Axel; Uribe, Lina M Moreno; Li, Xiao; Amendt, Brad; Cornell, Robert A

Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate

IRF6 和 TGFA 基因之间的相互作用会增加非综合征型唇腭裂的风险。

Letra, Ariadne; Fakhouri, Walid; Fonseca, Renata F; Menezes, Renato; Kempa, Inga; Prasad, Joanne L; McHenry, Toby G; Lidral, Andrew C; Moreno, Lina; Murray, Jeffrey C; Daack-Hirsch, Sandra; Marazita, Mary L; Castilla, Eduardo E; Lace, Baiba; Orioli, Ieda M; Granjeiro, Jose M; Schutte, Brian C; Vieira, Alexandre R

Genetic and environmental factors associated with dental caries in children: the Iowa Fluoride Study

与儿童龋齿相关的遗传和环境因素:爱荷华州氟化物研究

Wang, X; Willing, M C; Marazita, M L; Wendell, S; Warren, J J; Broffitt, B; Smith, B; Busch, T; Lidral, A C; Levy, S M