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

Associations of arsenic exposure and folate in maternal leukocyte DNA methylation: a case-control study of mothers with spina-bifida affected children

砷暴露和叶酸与母体白细胞DNA甲基化之间的关联:一项针对脊柱裂患儿母亲的病例对照研究

Inkster, Amy M; Bozack, Anne K; Lemos, Bernardo; Lumour-Mensah, Tabitha; Mukherjee, Sudipta Kumar; Ekramullah, Shekh Muhammad; Arman, D M; Islam, Joynul; Wang, Xingyan; Liang, Liming; Finnell, Richard H; Mazumdar, Maitreyi; Cardenas, Andres

Maternal Myo-Inositol Intake and Congenital Heart Defects in Offspring: A Population-Based Case-Control Study

母体肌醇摄入量与后代先天性心脏缺陷:一项基于人群的病例对照研究

Cen, Ruiqi; Su, L Joseph; Ying, Jun; Orloff, Mohammed S; Bolin, Elijah H; Lou, Xiangyang; Almli, Lynn M; Botto, Lorenzo D; Browne, Marilyn L; Finnell, Richard H; Jenkins, Mary M; Nestoridi, Eirini; Olshan, Andrew F; Romitti, Paul A; Shaw, Gary M; Nembhard, Wendy N

The contribution of de novo coding mutations to meningomyelocele

新发编码突变对脊髓脊膜膨出的影响

Ha, Yoo-Jin Jiny; Nisal, Ashna; Tang, Isaac; Lee, Chanjae; Jhamb, Ishani; Wallace, Cassidy; Howarth, Robyn; Schroeder, Sarah; Vong, Keng Ioi; Meave, Naomi; Jiwani, Fiza; Barrows, Chelsea; Lee, Sangmoon; Jiang, Nan; Patel, Arzoo; Bagga, Krisha; Banka, Niyati; Friedman, Liana; Blanco, Francisco A; Yu, Seyoung; Rhee, Soeun; Jeong, Hui Su; Plutzer, Isaac; Major, Michael B; Benoit, Béatrice; Poüs, Christian; Heffner, Caleb; Kibar, Zoha; Bot, Gyang Markus; Northrup, Hope; Au, Kit Sing; Strain, Madison; Ashley-Koch, Allison E; Finnell, Richard H; Le, Joan T; Meltzer, Hal S; Araujo, Camila; Machado, Helio R; Stevenson, Roger E; Yurrita, Anna; Mumtaz, Sara; Ahmed, Awais; Khara, Mulazim Hussain; Mutchinick, Osvaldo M; Medina-Bereciartu, José Ramón; Hildebrandt, Friedhelm; Melikishvili, Gia; Marwan, Ahmed I; Capra, Valeria; Noureldeen, Mahmoud M; Salem, Aida M S; Issa, Mahmoud Y; Zaki, Maha S; Xu, Libin; Lee, Ji Eun; Shin, Donghyuk; Alkelai, Anna; Shuldiner, Alan R; Kingsmore, Stephen F; Murray, Stephen A; Gee, Heon Yung; Miller, W Todd; Tolias, Kimberley F; Wallingford, John B; Kim, Sangwoo; Gleeson, Joseph G

Maternal Vitamin C Deficiency and Genetic Risk Factors Contribute to Congenital Defects through Dysregulation of DNA Methylation.

母体维生素 C 缺乏和遗传风险因素通过 DNA 甲基化失调导致先天缺陷

van der Veer Bernard K, Custers Colin, Brangers Wannes, Cornelis Riet, Tsaniras Spyridon Champeris, Ridder Kobe De, Thienpont Bernard, Cheng Huiyong, Chen Qiuying, Kraushaar Daniel, Finnell Richard H, Gross Steven S, Koh Kian Peng

Risk of meningomyelocele mediated by the common 22q11.2 deletion

常见的22q11.2缺失介导的脊髓脊膜膨出风险

Vong, Keng Ioi; Lee, Sangmoon; Au, Kit Sing; Crowley, T Blaine; Capra, Valeria; Martino, Jeremiah; Haller, Meade; Araújo, Camila; Machado, Hélio R; George, Renee; Gerding, Bryn; James, Kiely N; Stanley, Valentina; Jiang, Nan; Alu, Kameron; Meave, Naomi; Nidhiry, Anna S; Jiwani, Fiza; Tang, Isaac; Nisal, Ashna; Jhamb, Ishani; Patel, Arzoo; Patel, Aakash; McEvoy-Venneri, Jennifer; Barrows, Chelsea; Shen, Celina; Ha, Yoo-Jin; Howarth, Robyn; Strain, Madison; Ashley-Koch, Allison Elizabeth; Azam, Matloob; Mumtaz, Sara; Bot, Gyang Markus; Finnell, Richard H; Kibar, Zoha; Marwan, Ahmed I; Melikishvili, Gia; Meltzer, Hal S; Mutchinick, Osvaldo M; Stevenson, David A; Mroczkowski, Henry J; Ostrander, Betsy; Schindewolf, Erica; Moldenhauer, Julie; Zackai, Elaine H; Emanuel, Beverly S; Garcia-Minaur, Sixto; Nowakowska, Beata A; Stevenson, Roger E; Zaki, Maha S; Northrup, Hope; McNamara, Hanna K; Aldinger, Kimberly A; Phelps, Ian G; Deng, Mei; Glass, Ian A; Morrow, Bernice; McDonald-McGinn, Donna M; Sanna-Cherchi, Simone; Lamb, Dolores J; Gleeson, Joseph G

Mechanisms of neurodevelopmental toxicity of topiramate

托吡酯神经发育毒性的机制

Steele, John W; Krishnan, Vaishnav; Finnell, Richard H

Linkage between Fuz and Gpr161 genes regulates sonic hedgehog signaling during mouse neural tube development.

Fuz 和 Gpr161 基因之间的连锁作用调控小鼠神经管发育过程中的音猬因子信号传导

Kim Sung-Eun, Kim Hyun-Yi, Wlodarczyk Bogdan J, Finnell Richard H

Dolutegravir-induced neural tube defects in mice are folate responsive

多替拉韦诱导的小鼠神经管缺陷对叶酸有反应。

Tukeman, Gabriel L; Wei, Hui; Lin, Ying L; Wlodarczyk, Bogdan J; Finnell, Richard H; Cabrera, Robert M

Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study

外显子组测序在国家出生缺陷预防研究中发现了与原发性先天性青光眼相关的新基因

Blue, Elizabeth E; Moore, Kristin J; North, Kari E; Desrosiers, Tania A; Carmichael, Suzan L; White, Janson J; Chong, Jessica X; Bamshad, Michael J; Jenkins, Mary M; Almli, Lynn M; Brody, Lawrence C; Freedman, Sharon F; Reefhuis, Jennita; Romitti, Paul A; Shaw, Gary M; Werler, Martha; Kay, Denise M; Browne, Marilyn L; Feldkamp, Marcia L; Finnell, Richard H; Nembhard, Wendy N; Pangilinan, Faith; Olshan, Andrew F

Disruption of Fuz in mouse embryos generates hypoplastic hindbrain development and reduced cranial nerve ganglia

小鼠胚胎中Fuz基因的破坏会导致后脑发育不全和颅神经节减少。

Caiaffa, Carlo Donato; Ambekar, Yogeshwari S; Singh, Manmohan; Lin, Ying Linda; Wlodarczyk, Bogdan; Aglyamov, Salavat R; Scarcelli, Giuliano; Larin, Kirill V; Finnell, Richard H