I. Celine Hanson

Johns Hopkins University

H指数:40

被引数:7,862

个人简介

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教育背景

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工作经历

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荣誉奖项

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Cord blood transplantation for nonmalignant disorders: early functional immunity and high survival

BLOOD ADVANCES

IF7.1

2023-04-284

OAAI

Martinez, Caridad; Aguayo-Hiraldo, Paibel; Chaimowitz, Natalia; Forbes, Lisa; Rider, Nicholas; Nicholas, Sarah; Seeborg, Filiz; Chinen, Javier; Chinn, Ivan; Davis, Carla; Roseblatt, Howard; Noroski, Lenora; Omer, Bilal; John, Tami; Yassine, Khaled; Naik, Swati; Craddock, John; Bhar, Saleh; Allen, Carl; Ahmed, Nabil; Sasa, Ghadir; Steffin, David; Doherty, Erin; George, Anil; Salem, Baheyeldin; Friend, Brian; Hegde, Meenakshi; Brenner, Malcolm K.; Heslop, Helen E.; Leen, Ann; Pena, Amand; Wu, Mengfen; Hanson, I. Celine; Krance, Robert A.

FOXN1 forms higher-order nuclear condensates displaced by mutations causing immunodeficiency

SCIENCE ADVANCES

IF12.5

2021-12-0317

OAAI

Rota, Ioanna A.; Handel, Adam E.; Maio, Stefano; Klein, Fabian; Dhalla, Fatima; Deadman, Mary E.; Cheuk, Stanley; Newman, Joseph A.; Michaels, Yale S.; Zuklys, Saulius; Prevot, Nicolas; Hublitz, Philip; Charles, Philip D.; Gkazi, Athina Soragia; Adamopoulou, Eleni; Qasim, Waseem; Davies, Edward Graham; Hanson, Imelda; Pagnamenta, Alistair T.; Camps, Carme; Dreau, Helene M.; White, Andrea; James, Kieran; Fischer, Roman; Gileadi, Opher; Taylor, Jenny C.; Fulga, Tudor; Lagerholm, B. Christoffer; Anderson, Graham; Sezgin, Erdinc; Hollaender, Georg A.

Case Report: Secondary Hemophagocytic Lymphohistiocytosis With Disseminated Infection in Chronic Granulomatous Disease-A Serious Cause of Mortality

病例报告: 慢性肉芽肿病继发播散性感染的继发性噬血细胞性淋巴组织细胞增生症-死亡的严重原因

FRONTIERS IN IMMUNOLOGY

IF5.9

2020-12-097

OAAI

Disease-associated CTNNBL1 mutation impairs somatic hypermutation by decreasing nuclear AID

JOURNAL OF CLINICAL INVESTIGATION

IF13.6

2020-06-0219

The role of breast-feeding in cytomegalovirus transmission and hematopoietic stem cell transplant outcomes in infants with severe combined immunodeficiency

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE

IF6.6

2019-11-018

OAAI

Combined liver and hematopoietic stem cell transplantation in patients with X-linked hyper-IgM syndrome

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

IF11.2

2019-05-017

OAAI

Bucciol, Giorgia; Nicholas, Sarah K.; Calvo, Pier Luigi; Cant, Andrew; Edgar, J. David M.; Espanol, Teresa; Ferrua, Francesca; Galicchio, Miguel; Gennery, Andrew R.; Hadzic, Nedim; Hanson, I. Celine; Kusminsky, Gustavo; Lange, Andrzej; Lanternier, Fanny; Mahlaoui, Nizar; Moshous, Despina; Nademi, Zohreh; Neven, Benedicte; Oleastro, Matias; Porta, Fulvio; Quarello, Paola; Silva, Marcelo; Slatter, Mary A.; Soncini, Elena; Stefanowicz, Marek; Tandoi, Francesco; Teisseyre, Mikolaj; Torgerson, Troy R.; Veys, Paul; Weinacht, Katja G.; Wolska-Kusnierz, Beata; Pirenne, Jacques; de la Morena, M. Teresa; Meyts, Isabelle

In lasting tribute: William T. Shearer, August 23, 1937-October 9, 2018

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

IF11.2

2018-12-010

PREAI

Ruxolitinib partially reverses functional natural killer cell deficiency in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations

鲁索替尼部分逆转具有信号转导和转录激活因子1 (STAT1) 功能获得突变的患者的功能性自然杀伤细胞缺陷

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

IF11.2

2018-06-0176

OAAI

Novel Combined Immune Deficiency and Radiation sensitivity Blended phenotype in an adult with Biallelic Variations in ZAP70 and RNF168

FRONTIERS IN IMMUNOLOGY

IF5.9

2017-05-2618

OAAI

Ruxolitinib reverses dysregulated T helper cell responses and controls autoimmunity caused by a novel signal transducer and activator of transcription 1 (STAT1) gain-of-function mutation

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

IF11.2

2017-05-01123

OAAI

Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

IF11.2

2017-04-0186

OAAI

de la Morena, M. Teresa; Leonard, David; Torgerson, Troy R.; Cabral-Marques, Otavio; Slatter, Mary; Aghamohammadi, Asghar; Chandra, Sharat; Murguia-Favela, Luis; Bonilla, Francisco A.; Kanariou, Maria; Damrongwatanasuk, Rongras; Kuo, Caroline Y.; Dvorak, Christopher C.; Meyts, Isabelle; Chen, Karin; Kobrynski, Lisa; Kapoor, Neena; Richter, Darko; DiGiovanni, Daniela; Dhalla, Fatima; Farmaki, Evangelia; Speckmann, Carsten; Espanol, Teresa; Shcherbina, Anna; Hanson, Imelda Celine; Litzman, Jiri; Routes, John M.; Wong, Melanie; Fuleihan, Ramsay; Seneviratne, Suranjith L.; Small, Trudy N.; Janda, Ales; Bezrodnik, Liliana; Seger, Reinhard; Raccio, Andrea Gomez; Edgar, J. David M.; Chou, Janet; Abbott, Jordan K.; van Montfrans, Joris; Gonzalez-Granado, Luis Ignacio; Bunin, Nancy; Kutukculer, Necil; Gray, Paul; Seminario, Gisela; Pasic, Srdjan; Aquino, Victor; Wysocki, Christian; Abolhassani, Hassan; Dorsey, Morna; Cunningham-Rundles, Charlotte; Knutsen, Alan P.; Sleasman, John; Carvalho, Beatriz Tavares Costa; Condino-Neto, Antonio; Grunebaum, Eyal; Chapel, Helen; Ochs, Hans D.; Filipovich, Alexandra; Cowan, Mort; Gennery, Andrew; Cant, Andrew; Notarangelo, Luigi D.; Roifman, Chaim M.

Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

IF11.2

2017-01-01214

OAAI

Stray-Pedersen, Asbjorg; Sorte, Hanne Sormo; Samarakoon, Pubudu; Gambin, Tomasz; Chinn, Ivan K.; Akdemir, Zeynep H. Coban; Erichsen, Hans Christian; Forbes, Lisa R.; Gu, Shen; Yuan, Bo; Jhangiani, Shalini N.; Muzny, Donna M.; Rodningen, Olaug Kristin; Sheng, Ying; Nicholas, Sarah K.; Noroski, Lenora M.; Seeborg, Filiz O.; Davis, Carla M.; Canter, Debra L.; Mace, Emily M.; Vece, Timothy J.; Allen, Carl E.; Abhyankar, Harshal A.; Boone, Philip M.; Beck, Christine R.; Wiszniewski, Wojciech; Fevang, Borre; Aukrust, Pal; Tjonnfjord, Geir E.; Gedde-Dahl, Tobias; Hjorth-Hansen, Henrik; Dybedal, Ingunn; Nordoy, Ingvild; Jorgensen, Silje F.; Abrahamsen, Tore G.; Overland, Torstein; Bechensteen, Anne Grete; Skogen, Vegard; Osnes, Liv T. N.; Kulseth, Mari Ann; Prescott, Trine E.; Rustad, Cecilie F.; Heimdal, Ketil R.; Belmont, John W.; Rider, Nicholas L.; Chinen, Javier; Cao, Tram N.; Smith, Eric A.; Soledad Caldirola, Maria; Bezrodnik, Liliana; Lugo Reyes, Saul Oswaldo; Espinosa Rosales, Francisco J.; Guerrero-Cursaru, Nina Denisse; Pedroza, Luis Alberto; Poli, Cecilia M.; Franco, Jose L.; Trujillo Vargas, Claudia M.; Aldave Becerra, Juan Carlos; Wright, Nicola; Issekutz, Thomas B.; Issekutz, Andrew C.; Abbott, Jordan; Caldwell, Jason W.; Bayer, Diana K.; Chan, Alice Y.; Aiuti, Alessandro; Cancrini, Caterina; Holmberg, Eva; West, Christina; Burstedt, Magnus; Karaca, Ender; Yesil, Gozde; Artac, Hasibe; Bayram, Yavuz; Atik, Mehmed Musa; Eldomery, Mohammad K.; Ehlayel, Mohammad S.; Jolles, Stephen; Flato, Berit; Bertuch, Alison A.; Hanson, I. Celine; Zhang, Victor W.; Wong, Lee-Jun; Hu, Jianhong; Walkiewicz, Magdalena; Yang, Yaping; Eng, Christine M.; Boerwinkle, Eric; Gibbs, Richard A.; Shearer, William T.; Lyle, Robert; Orange, Jordan S.; Lupski, James R.

Rapid molecular diagnostics of severe primary immunodeficiency determined by using targeted next-generation sequencing

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

IF11.2

2016-10-0160

PREAI

A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

IF11.2

2016-08-0120

OAAI

Adoptive immunotherapy for primary immunodeficiency disorders with virus-specific T lymphocytes

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY