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Ali Sobh

Observed names: A Sobh, Ali Abd-Elwahab Sobh, Ali Abdelwahab Sobh, Ali Sobh (13566367), Sobh, Ali
Observed institutions: Boston Children's Hospital, Harvard University, University of Leicester, Vita-Salute San Raffaele University, Mansoura University, Chungnam National University, Tanta University, Hospital Universitario La Paz, Newcastle upon Tyne Hospitals NHS Foundation Trust, Masih Daneshvari Hospital, Children's Hospital Mansoura University, Mansoura University Hospital, Hospital La Paz Institute for Health Research, Newcastle upon Tyne Hospital, IRCCS Ospedale San Raffaele, Great North Children's Hospital, Chungnam National University Hospital, Shahid Beheshti University of Medical Sciences, University of Brescia
ORCID: 0000-0001-7047-076X
Observed ORCID: 0000-0001-7047-076X
OpenAlex ID: A5037434440
Autoantibodies against type I IFNs in patients with life-threatening COVID-19
2020 · Paul Bastard, Lindsey B. Rosen, et al. · Science · 2,661
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
2020 · Qian Zhang, Paul Bastard, et al. · Science · 2,229
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Whole-genome sequencing reveals host factors underlying critical COVID-19
2022 · Athanasios Kousathanas, Erola Pairo-Castineira, et al. · Nature · 327
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The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies
2022 · Jérémy Manry, Paul Bastard, et al. · Proceedings of the National Academy of Sciences · 193
A first update on mapping the human genetic architecture of COVID-19
2022 · COVID-19 Host Genetics Initiative, COVID-19 Host Genetics Initiative, et al. · Nature · 181
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Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations
2021 · Julian Thalhammer, Gerhard Kindle, et al. · Journal of Allergy and Clinical Immunology · 171
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Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children
2022 · Danyel Lee, Jérémie Le Pen, et al. · Science · 159
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Genotype and functional correlates of disease phenotype in deficiency of adenosine deaminase 2 (DADA2)
2020 · Pui Y. Lee, Erinn S. Kellner, et al. · Journal of Allergy and Clinical Immunology · 150
SARS-CoV-2–related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
2021 · Vanessa Sancho-Shimizu, Petter Brodin, et al. · The Journal of Experimental Medicine · 147
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A second update on mapping the human genetic architecture of COVID-19
2023 · The COVID-19 Host Genetics Initiative, Leadership, et al. · Nature · 121
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Vaccination in Primary Immunodeficiency Disorders
2016 · Ali Sobh, Francisco A. Bonilla · The Journal of Allergy and Clinical Immunology In Practice · 117
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
2023 · Daniela Matuozzo, Estelle Talouarn, et al. · Genome Medicine · 80
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Consensus Middle East and North Africa Registry on Inborn Errors of Immunity
2021 · Asghar Aghamohammadi, Nima Rezaei, et al. · Journal of Clinical Immunology · 79
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The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity
2022 · Safa Baris, Hassan Abolhassani, et al. · The Journal of Allergy and Clinical Immunology In Practice · 60
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Inborn errors of immunity: Manifestation, treatment, and outcome—an ESID registry 1994–2024 report on 30,628 patients
2025 · Gerhard Kindle, Mickaël Alligon, et al. · Journal of Human Immunity · 46
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Current treatment in macrophage activation syndrome worldwide: a systematic literature review to inform the METAPHOR project
2024 · Francesco Baldo, Remco G A Erkens, et al. · Lara D. Veeken · 46
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
2021 · Matteo D’Antonio, Jennifer P. Nguyen, et al. · Cell Reports · 45
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Outcome of autoimmune cytopenia after hematopoietic cell transplantation in primary immunodeficiency
2020 · Su Han Lum, Sabeena Selvarajah, et al. · Journal of Allergy and Clinical Immunology · 29
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SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency
2024 · Yi-Hao Chan, Vanja Lundberg, et al. · The Journal of Experimental Medicine · 22
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Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry
2022 · Mahnaz Jamee, Gholamreza Azizi, et al. · Clinical Immunology · 20
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Regulatory T-cell dysfunction and cutaneous exposure to Staphylococcus aureus underlie eczema in DOCK8 deficiency
2024 · Hazel Wilkie, Mrinmoy Das, et al. · Journal of Allergy and Clinical Immunology · 19
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DOCK8 is essential for LFA-1–dependent positioning of T follicular helper cells in germinal centers
2020 · Erin Janssen, Mira Tohme, et al. · JCI Insight · 19
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Autoimmune lymphoproliferative syndrome caused by a homozygous FasL mutation that disrupts FasL assembly
2015 · Ali Sobh, Elena Crestani, et al. · Journal of Allergy and Clinical Immunology · 19
Genetic association of ACE2 and TMPRSS2 polymorphisms with COVID-19 severity; a single centre study from Egypt
2024 · Marwa H. Elnagdy, Alshimaa Magdy, et al. · Virology Journal · 18
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Chronic mucocutaneous candidiasis associated with an SH2 domain gain-of-function mutation that enhances STAT1 phosphorylation
2016 · Ali Sobh, Janet Chou, et al. · Journal of Allergy and Clinical Immunology · 18
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Works count: 84
Citation count: 7,151
H-index: 20
I10-index: 32
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