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

The Genetic Architecture of Congenital Diarrhea and Enteropathy

先天性腹泻和肠病的遗传结构

Gaibee, Zeenat; Warner, Neil; Bugda Gwilt, Katlynn; Li, Wenjuan; Guan, Rei; Yourshaw, Michael; Whittaker Hawkins, Ryder; Zorbas, Christiane; St-Germain, Jonathan; Tabatabaie, Mahdi; Mao, Suli; Pinsk, Vered; Yerushalmi, Baruch; Wang, Lee-Kai; Nelson, Stanley F; Wozniak, Laura; Shouval, Dror S; Matar, Manar; Assa, Amit; Frost, Nathaniel; Jimenez, Lissette; Acra, Sari; Walters, Thomas; Mouat, Stephen; Li, Michael; Lafontaine, Denis L J; Tyska, Matthew; Raught, Brian; Avitzur, Yaron; Lencer, Wayne I; Goldenring, James R; Martín, Martín G; Thiagarajah, Jay R; Muise, Aleixo M

"Deficiency in ELF4, X-Linked": a Monogenic Disease Entity Resembling Behçet's Syndrome and Inflammatory Bowel Disease

“ELF4基因缺陷,X连锁”:一种类似于白塞氏病和炎症性肠病的单基因疾病

Olyha, Sam J; O'Connor, Shannon K; Kribis, Marat; Bucklin, Molly L; Uthaya Kumar, Dinesh Babu; Tyler, Paul M; Alam, Faiad; Jones, Kate M; Sheikha, Hassan; Konnikova, Liza; Lakhani, Saquib A; Montgomery, Ruth R; Catanzaro, Jason; Du, Hongqiang; DiGiacomo, Daniel V; Rothermel, Holly; Moran, Christopher J; Fiedler, Karoline; Warner, Neil; Hoppenreijs, Esther P A H; van der Made, Caspar I; Hoischen, Alexander; Olbrich, Peter; Neth, Olaf; Rodríguez-Martínez, Alejandro; Lucena Soto, José Manuel; van Rossum, Annemarie M C; Dalm, Virgil A S H; Muise, Aleixo M; Lucas, Carrie L

Landscape of TPMT and NUDT15 Pharmacogenetic Variation in a Cohort of Canadian Pediatric Inflammatory Bowel Disease Patients

加拿大儿童炎症性肠病患者队列中TPMT和NUDT15药物遗传变异的分布情况

Kennedy, April M; Griffiths, Anne M; Muise, Aleixo M; Walters, Thomas D; Ricciuto, Amanda; Huynh, Hien Q; Wine, Eytan; Jacobson, Kevan; Lawrence, Sally; Carman, Nicholas; Mack, David R; deBruyn, Jennifer C; Otley, Anthony R; Deslandres, Colette; El-Matary, Wael; Zachos, Mary; Benchimol, Eric I; Critch, Jeffrey; Schneider, Rilla; Crowley, Eileen; Li, Michael; Warner, Neil; McGovern, Dermot P B; Li, Dalin; Haritunians, Talin; Rudin, Sarah; Cohn, Iris

Chromosomal Numerical Aberrations and Rare Copy Number Variation in Patients with Inflammatory Bowel Disease

炎症性肠病患者的染色体数目异常和罕见拷贝数变异

Dirvanskyte, Paulina; Gurram, Bhaskar; Bolton, Chrissy; Warner, Neil; Jones, Kelsey D J; Griffin, Helen R; Park, Jason Y; Keller, Klaus-Michael; Gilmour, Kimberly C; Hambleton, Sophie; Muise, Aleixo M; Wysocki, Christian; Uhlig, Holm H

The Diverse Phenotype of Intestinal Dysmotility Secondary to ACTG2-related Disorders

ACTG2相关疾病引起的肠道动力障碍的多样化表型

Sandy, Natascha S; Huysentruyt, Koen; Mulder, Daniel J; Warner, Neil; Chong, Karen; Morel, Chantal; AlQahtani, Saleh; Wales, Paul W; Martin, Martin G; Muise, Aleixo M; Avitzur, Yaron

A Machine Learning Approach to Identifying Causal Monogenic Variants in Inflammatory Bowel Disease

利用机器学习方法识别炎症性肠病中的致病单基因变异

Mulder, Daniel J; Khalouei, Sam; Li, Michael; Warner, Neil; Gonzaga-Jauregui, Claudia; Benchimol, Eric I; Church, Peter C; Walters, Thomas D; Ramani, Arun K; Griffiths, Anne M; Ricciuto, Amanda; Muise, Aleixo M

Human autoinflammatory disease reveals ELF4 as a transcriptional regulator of inflammation

人类自身炎症性疾病揭示了ELF4作为炎症转录调节因子的作用。

Tyler, Paul M; Bucklin, Molly L; Zhao, Mengting; Maher, Timothy J; Rice, Andrew J; Ji, Weizhen; Warner, Neil; Pan, Jie; Morotti, Raffaella; McCarthy, Paul; Griffiths, Anne; van Rossum, Annemarie M C; Hollink, Iris H I M; Dalm, Virgil A S H; Catanzaro, Jason; Lakhani, Saquib A; Muise, Aleixo M; Lucas, Carrie L

Variants in STXBP3 are Associated with Very Early Onset Inflammatory Bowel Disease, Bilateral Sensorineural Hearing Loss and Immune Dysregulation.

STXBP3 的变异与极早期发病的炎症性肠病、双侧感觉神经性听力损失和免疫失调有关

Ouahed Jodie, Kelsen Judith R, Spessott Waldo A, Kooshesh Kameron, Sanmillan Maria L, Dawany Noor, Sullivan Kathleen E, Hamilton Kathryn E, Slowik Voytek, Nejentsev Sergey, Neves João Farela, Flores Helena, Chung Wendy K, Wilson Ashley, Anyane-Yeboa Kwame, Wou Karen, Jain Preti, Field Michael, Tollefson Sophia, Dent Maiah H, Li Dalin, Naito Takeo, McGovern Dermot P B, Kwong Andrew C, Taliaferro Faith, Ordovas-Montanes Jose, Horwitz Bruce H, Kotlarz Daniel, Klein Christoph, Evans Jonathan, Dorsey Jill, Warner Neil, Elkadri Abdul, Muise Aleixo M, Goldsmith Jeffrey, Thompson Benjamin, Engelhardt Karin R, Cant Andrew J, Hambleton Sophie, Barclay Andrew, Toth-Petroczy Agnes, Vuzman Dana, Carmichael Nikkola, Bodea Corneliu, Cassa Christopher A, Devoto Marcella, Maas Richard L, Behrens Edward M, Giraudo Claudio G, Snapper Scott B

Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease

NOD2基因突变谱揭示隐性遗传是早发性克罗恩病的主要驱动因素

Horowitz, Julie E; Warner, Neil; Staples, Jeffrey; Crowley, Eileen; Gosalia, Nehal; Murchie, Ryan; Van Hout, Cristopher; Fiedler, Karoline; Welch, Gabriel; King, Alejandra Klauer; Reid, Jeffrey G; Overton, John D; Baras, Aris; Shuldiner, Alan R; Griffiths, Anne; Gottesman, Omri; Muise, Aleixo M; Gonzaga-Jauregui, Claudia

Does HPV Subtype Predict Outcomes in Head and Neck Cancers?

HPV 亚型可以预测头颈癌的结果吗?

Hedyeh Ziai, Andrew Warner, Neil Mundi, Krupal Patel, Eun Jae Chung, Christopher J Howlett, Paul Plantinga, John Yoo, S Danielle MacNeil, Kevin Fung, Joe S Mymryk, John W Barrett, David A Palma, Anthony C Nichols