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

Testing the performance of polygenic scores for multiple traits to explain cerebral palsy in two independent cohorts

在两个独立的队列中检验多基因评分对多种性状解释脑瘫的性能

Thomas, Jodi T; Berry, Alexander S F; Oetjens, Matthew T; Berry, Jesia G; MacLennan, Alastair H; Gordon, Scott D; Hale, Andrew T; Olsen, Catherine M; Whiteman, David C; Torene, Rebecca I; Ledbetter, David H; Martin, Nicholas G; van Eyk, Clare L; Gecz, Jozef; Myers, Scott M; Mitchell, Brittany L; Corbett, Mark A

First-principles optimization of thermoelectric and optoelectronic performance of KSn(1-x) Zn (x) I(3) (x = 0, 0.25, 0.5, 0.75, 1) perovskites for sustainable energy harvesting

基于第一性原理的KSn(1-x)Zn(x)I(3) (x = 0, 0.25, 0.5, 0.75, 1)钙钛矿热电和光电性能优化及其在可持续能量收集中的应用

Ahmed, Usama; Sayem Rahman, Abu Sadat Md; Jui, Jesia Alam; Hossain, Md Mukter; Uddin, Md Mohi; Ali, Md Ashraf

Optimal Treatment of Retinal Vein Occlusion: An Updated Canadian Review and Recommendations

视网膜静脉阻塞的最佳治疗:加拿大最新综述和建议

Sivachandran, Nirojini; Altomare, Filiberto; Dookeran, Ravi; Hasan, Jesia; Whelan, James H

Genetic diagnostic yield by MRI pattern in children with cerebral palsy: a population-based study

脑瘫患儿MRI模式的基因诊断率:一项基于人群的研究

Berry, Jesia G; Taranath, Ajay; Goetti, Robert; Farrar, Michelle A; Fiori, Simona; Pham, Huy-Dat; Mittinty, Murthy N; Corbett, Mark A; Palmer, Lyle J; Fornarino, Dani L; Harper, Kelly; Gibson, Catherine S; Leishman, Shaneen J; Goldsmith, Shona C; McIntyre, Sarah J; Montgomerie, Alicia; Pilkington, Rhiannon M; Lynch, John W; Russo, Remo N; Fahey, Michael C; Fripp, Jurgen; Boyd, Roslyn N; Wright, Margaret J; Rice, James E; Waugh, Mary-Clare; MacLennan, Alastair H; Gecz, Jozef; van Eyk, Clare L

The 'Floating Medial Meniscus' Lesion in KD3M Knee Dislocations

KD3M型膝关节脱位中的“内侧半月板漂浮”损伤

Pardiwala, Dinshaw N; Desouza, Clevio; Jesia, Arzan

The Treatment Algorithm for Chronic Multiple Ligament Knee Injury

慢性多韧带膝关节损伤的治疗流程

Pardiwala, Dinshaw N; Desouza, Clevio; Jesia, Arzan

Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss

SPATA5L1基因的双等位基因变异会导致智力障碍、痉挛性肌张力障碍性脑瘫、癫痫和听力丧失。

Richard, Elodie M; Bakhtiari, Somayeh; Marsh, Ashley P L; Kaiyrzhanov, Rauan; Wagner, Matias; Shetty, Sheetal; Pagnozzi, Alex; Nordlie, Sandra M; Guida, Brandon S; Cornejo, Patricia; Magee, Helen; Liu, James; Norton, Bethany Y; Webster, Richard I; Worgan, Lisa; Hakonarson, Hakon; Li, Jiankang; Guo, Yiran; Jain, Mahim; Blesson, Alyssa; Rodan, Lance H; Abbott, Mary-Alice; Comi, Anne; Cohen, Julie S; Alhaddad, Bader; Meitinger, Thomas; Lenz, Dominic; Ziegler, Andreas; Kotzaeridou, Urania; Brunet, Theresa; Chassevent, Anna; Smith-Hicks, Constance; Ekstein, Joseph; Weiden, Tzvi; Hahn, Andreas; Zharkinbekova, Nazira; Turnpenny, Peter; Tucci, Arianna; Yelton, Melissa; Horvath, Rita; Gungor, Serdal; Hiz, Semra; Oktay, Yavuz; Lochmuller, Hanns; Zollino, Marcella; Morleo, Manuela; Marangi, Giuseppe; Nigro, Vincenzo; Torella, Annalaura; Pinelli, Michele; Amenta, Simona; Husain, Ralf A; Grossmann, Benita; Rapp, Marion; Steen, Claudia; Marquardt, Iris; Grimmel, Mona; Grasshoff, Ute; Korenke, G Christoph; Owczarek-Lipska, Marta; Neidhardt, John; Radio, Francesca Clementina; Mancini, Cecilia; Claps Sepulveda, Dianela Judith; McWalter, Kirsty; Begtrup, Amber; Crunk, Amy; Guillen Sacoto, Maria J; Person, Richard; Schnur, Rhonda E; Mancardi, Maria Margherita; Kreuder, Florian; Striano, Pasquale; Zara, Federico; Chung, Wendy K; Marks, Warren A; van Eyk, Clare L; Webber, Dani L; Corbett, Mark A; Harper, Kelly; Berry, Jesia G; MacLennan, Alastair H; Gecz, Jozef; Tartaglia, Marco; Salpietro, Vincenzo; Christodoulou, John; Kaslin, Jan; Padilla-Lopez, Sergio; Bilguvar, Kaya; Munchau, Alexander; Ahmed, Zubair M; Hufnagel, Robert B; Fahey, Michael C; Maroofian, Reza; Houlden, Henry; Sticht, Heinrich; Mane, Shrikant M; Rad, Aboulfazl; Vona, Barbara; Jin, Sheng Chih; Haack, Tobias B; Makowski, Christine; Hirsch, Yoel; Riazuddin, Saima; Kruer, Michael C

Erratum: Author Correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy

勘误:作者更正:影响基因表达的致病性拷贝数变异会导致脑瘫患者的基因组负担。

Corbett, Mark A; van Eyk, Clare L; Webber, Dani L; Bent, Stephen J; Newman, Morgan; Harper, Kelly; Berry, Jesia G; Azmanov, Dimitar N; Woodward, Karen J; Gardner, Alison E; Slee, Jennie; Pérez-Jurado, Luís A; MacLennan, Alastair H; Gecz, Jozef

Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy

影响基因表达的致病性拷贝数变异会导致脑瘫患者的基因组负担加重。

Corbett, Mark A; van Eyk, Clare L; Webber, Dani L; Bent, Stephen J; Newman, Morgan; Harper, Kelly; Berry, Jesia G; Azmanov, Dimitar N; Woodward, Karen J; Gardner, Alison E; Slee, Jennie; Pérez-Jurado, Luís A; MacLennan, Alastair H; Gecz, Jozef

Evolution of Geographic Atrophy in Participants Treated with Ranibizumab for Neovascular Age-related Macular Degeneration

接受雷珠单抗治疗的新生血管性年龄相关性黄斑变性患者的地图状萎缩演变

Thavikulwat, Alisa T; Jacobs-El, Naima; Kim, Jane S; Agrón, Elvira; Hasan, Jesia; Meyerle, Catherine B; Valent, David; Cukras, Catherine A; Wiley, Henry E; Wong, Wai T; Chew, Emily Y