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

Proceedings of the second Artificial Intelligence in Primary Immunodeficiency (AIPI) meeting

第二届原发性免疫缺陷人工智能(AIPI)会议论文集

Rivière, Jacques G; Bastarache, Lisa; Campos, Luiza C; Carot-Sans, Gerard; Chin, Aaron; Chunara, Rumi; Cunningham-Rundles, Charlotte; Erra, Lorenzo; Farmer, Jocelyn; Garcelon, Nicolas; Hsieh, Elena; Leavis, Helen; Lee, Seungwon; Liu, Liangying; Kusters, Maaike; Lloyd, Brian C; Martinson, Alexandra K; Mester, Rachel; Moore, Justin B; Moshous, Despina; Orange, Jordan S; Parrish, Nefatia; Parker, Sarah Henrickson; Pasaniuc, Bogdan; Peng, Xiao P; Pergent, Martine; Piera-Jiménez, Jordi; Quinn, Jessica; Ramesh, Sidharth; Roberts, Kirk; Robinson, Peter N; Savova, Guergana; Scalchunes, Christopher; Seidel, Markus G; Simoneau, Rachel; Soler-Palacin, Pere; Sullivan, Kathleen E; Van Gijn, Marielle; Wi, Chung-Il; Zhou, Dawei; Tenembaum, Vanessa; Butte, Manish J; Rider, Nicholas L

Heterozygous NFKB1 variant causes inflammatory dysregulation shaped by broader genetic context in common variable immunodeficiency

杂合子 NFKB1 变异导致炎症失调,这种失调受常见变异型免疫缺陷更广泛的遗传背景影响。

Hayes, Kevin M; Boldt, Kai; Schnorr, Peter J; Bawa, Pushpinder; Abyazi, Miranda L; Ware, Matthew S; Gyimesi, Gavin; James, Marianne; Ko, Huaibin M; Cunningham-Rundles, Charlotte; Mizgerd, Joseph P; Mostoslavsky, Gustavo; Kotton, Darrell N; Maglione, Paul J

Homozygosity for rare or common hypomorphic IL23R variants confers a predisposition to tuberculosis in humans

人类携带罕见或常见的低活性IL23R变异纯合子会增加患结核病的易感性。

Calderón, Diana Olguín; Kilpatrick, Laura E; Conil, Clément; Philippot, Quentin; Ogishi, Masato; Vellutini, Joseph; Han, Ji Eun; Keating, Narelle; Li, Hailun; Rao, Geetha; Bohlen, Jonathan; Lay, Charles S; Platt, Simon; Kerner, Gaspard; Feredj, Elsa; Peel, Jessica N; Momenilandi, Mana; Seeleuthner, Yoann; Lainé, Candice; Soudée, Camille; Leloup, Claire; Debuisson, Cecile; Lanternier, Fanny; Bitoun, Samuel; Pavy, Stephan; Mariette, Xavier; Rafik, Aniss; Skhoun, Hanaa; El Ouazzani, Hanane; Abderahmani-Ghorfi, Ismail; El-Bagdadi, Jamila; Baena, Andrés; Tejada-Giraldo, Manuela; Barrera, Luis Fernando; Arias, Andrés Augusto; Fabio, Giovanna; Carrabba, Maria; Emiroglu, Melike; Bezrodnik, Liliana; El Zein, Loubna; Hammoud, Hassan; Gregersen, Peter K; Terrier, Benjamin; Lopez, Rafael Leon; Touzet, Marion; Pestre, Vincent; Pasquet, Marlène; Rogge, Lars; Pasquet, Marlène; Fayon, Michael; Galode, François; Jeziorski, Eric; Duffy, Daragh; Quintana-Murci, Lluis; Patin, Etienne; Cunningham-Rundles, Charlotte; Meyts, Isabelle; Zhang, Shen-Ying; Zhang, Qian; Jouanguy, Emmanuelle; Boisson, Bertrand; Rosain, Jérémie; Béziat, Vivien; Shahrooei, Mohammad; Mahdaviani, Seyed Alireza; Rezaei, Nima; Parvaneh, Nima; Chavoshzadeh, Zahra; Yazdanpanah, Niloufar; Aladjidi, Nathalie; Noguera-Julian, Antoni; Esteve-Solé, Ana; Manrique, Laia Alsina; Mansouri, Davood; Keles, Sevgi; Ortakoylu, Mediha Gonenc; Aygun, Deniz; Yucel, Esra; Kiykim, Ayca; Camcioglu, Yildiz; Ma, Cindy S; Tangye, Stuart G; Zhang, Peng; Abel, Laurent; Craggs, Peter D; Casanova, Jean-Laurent; Cobat, Aurélie; Puel, Anne; Bustamante, Jacinta; Hill, Stephen J; Boisson-Dupuis, Stéphanie

Common Variable Immunodeficiency Clinical Manifestations Are Shaped by Presence and Type of Heterozygous NFKB1 Variants.

常见变异型免疫缺陷的临床表现取决于杂合NFKB1变异的存在和类型

Yin Jie, Hayes Kevin M, Ong Mei-Sing, Mizgerd Joseph P, Cunningham-Rundles Charlotte, Dominguez Isabel, Barmettler Sara, Farmer Jocelyn R, Maglione Paul J

Primary versus Secondary Immune Thrombocytopenia (ITP): A Meeting Report from the 2023 McMaster ITP Summit

原发性与继发性免疫性血小板减少症 (ITP):2023 年麦克马斯特大学 ITP 峰会会议报告

Modi, Dimpy; Chowdhury, Saifur R; Mahamad, Syed; Modi, Hayley; Cines, Douglas B; Neunert, Cindy E; Al-Samkari, Hanny; Cooper, Nichola; Moulis, Guillaume; Cunningham-Rundles, Charlotte; Liebman, Howard A; Bussel, James B; Breakey, Vicky R; Nazy, Ishac; Arnold, Donald M

Re-evaluation of the contribution of TNFRSF13B variants to antibody deficiency

重新评估TNFRSF13B变异体对抗体缺乏症的影响

Abolhassani, Hassan; Caballero-Oteyza, Andres; Yang, Mingyu; Proietti, Michele; Delavari, Samaneh; Maffucci, Patrick; Schäffer, Alejandro A; Boisson, Bertrand; Casanova, Jean-Laurent; Rezaei, Nima; Pan-Hammarström, Qiang; Cunningham-Rundles, Charlotte; Hammarström, Lennart; Grimbacher, Bodo

Refractory marginal zone lymphoma uncovers activated phosphoinositide 3-kinase delta syndrome type 1 (APDS1)

难治性边缘区淋巴瘤揭示活化磷脂酰肌醇3-激酶δ综合征1型(APDS1)

Wonnaparhown, Alex; Farley, Matthew; Miller, Holly; Cunningham-Rundles, Charlotte; Freeman, Catherine; Squire, Jacqueline; Hilal, Talal; Rosenthal, Allison

The 2024 update of IUIS phenotypic classification of human inborn errors of immunity

2024年国际免疫学会(IUIS)人类先天性免疫缺陷表型分类更新

Bousfiha, Ahmed Aziz; Jeddane, Leïla; Moundir, Abderrahmane; Poli, M Cecilia; Aksentijevich, Ivona; Cunningham-Rundles, Charlotte; Hambleton, Sophie; Klein, Christoph; Morio, Tomohiro; Picard, Capucine; Puel, Anne; Rezaei, Nima; Seppänen, Mikko R J; Somech, Raz; Su, Helen C; Sullivan, Kathleen E; Torgerson, Troy R; Tangye, Stuart G; Meyts, Isabelle

Human inborn errors of immunity: 2024 update on the classification from the International Union of Immunological Societies Expert Committee

人类先天性免疫缺陷:国际免疫学会联盟专家委员会2024年分类更新

Poli, M Cecilia; Aksentijevich, Ivona; Bousfiha, Ahmed Aziz; Cunningham-Rundles, Charlotte; Hambleton, Sophie; Klein, Christoph; Morio, Tomohiro; Picard, Capucine; Puel, Anne; Rezaei, Nima; Seppänen, Mikko R J; Somech, Raz; Su, Helen C; Sullivan, Kathleen E; Torgerson, Troy R; Meyts, Isabelle; Tangye, Stuart G

Disease diagnostics using machine learning of B cell and T cell receptor sequences

利用机器学习技术对B细胞和T细胞受体序列进行疾病诊断

Zaslavsky, Maxim E; Craig, Erin; Michuda, Jackson K; Sehgal, Nidhi; Ram-Mohan, Nikhil; Lee, Ji-Yeun; Nguyen, Khoa D; Hoh, Ramona A; Pham, Tho D; Röltgen, Katharina; Lam, Brandon; Parsons, Ella S; Macwana, Susan R; DeJager, Wade; Drapeau, Elizabeth M; Roskin, Krishna M; Cunningham-Rundles, Charlotte; Moody, M Anthony; Haynes, Barton F; Goldman, Jason D; Heath, James R; Chinthrajah, R Sharon; Nadeau, Kari C; Pinsky, Benjamin A; Blish, Catherine A; Hensley, Scott E; Jensen, Kent; Meyer, Everett; Balboni, Imelda; Utz, Paul J; Merrill, Joan T; Guthridge, Joel M; James, Judith A; Yang, Samuel; Tibshirani, Robert; Kundaje, Anshul; Boyd, Scott D