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Jessica Willett Pachul

Observed names: Jessica Willet Pachul, Jessica Willett-Pachul, Jessica Willett Pachul
OpenAlex ID: A5068544805
DNA‐Binding domain mutations confer severe outcome at an early age among STAT1 gain‐of‐function patients
2021 · Ori Scott, Harjit Dadi, et al. · Pediatric Allergy and Immunology · 19
Case Report: Eosinophilic Esophagitis in a Patient With a Novel STAT1 Gain-of-Function Pathogenic Variant
2022 · Ori Scott, Nigel Sharfe, et al. · Frontiers in Immunology · 13
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Homozygous duplication identified by whole genome sequencing causes LRBA deficiency
2021 · Daniele Merico, Yehonatan Pasternak, et al. · npj Genomic Medicine · 10
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A Unique Comprehensive Model to Screen Newborns for Severe Combined Immunodeficiency—An Ontario Single-Centre Experience Spanning 2013–2023
2024 · Abdulrahman Al Ghamdi, Jessica Willett Pachul, et al. · Genes · 6
A novel mutation in TRAC in a patient with abnormal newborn screening for severe combined immunodeficiency
2022 · Jenny Garkaby, Laura Edith Abrego Fuentes, et al. · LymphoSign Journal · 6
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A novel splice site variant in FOXN1 in a patient with abnormal newborn screening for severe combined immunodeficiency and congenital lymphopenia
2021 · Ori Scott, Jenny Garkaby, et al. · LymphoSign Journal · 6
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Utilization of next-generation sequencing to define the role of heterozygous FOXN1 variants in immunodeficiency
2024 · Yehonatan Pasternak, Linda Vong, et al. · Journal of Allergy and Clinical Immunology Global · 3
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Novel heterozygous FOXN1 mutation identified following newborn screening for severe combined immunodeficiency is associated with improving immune parameters
2022 · Laura Edith Abrego Fuentes, Jenny Garkaby, et al. · LymphoSign Journal · 3
Novel mutation in PIK3CD affecting the Ras-binding domain
2022 · Laura Abrego Fuentes, Jenny Garkaby, et al. · LymphoSign Journal · 3
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Utilization of Next Generation Sequencing to Define the Role of Heterozygous FOXN1 Mutations in Immune Disorders
2024 · Yehonatan Pasternak, Linda Vong, et al. · Journal of Allergy and Clinical Immunology · 2
Favorable outcome of COVID ‐19 in pediatric patients with primary immunodeficiency
2023 · Jenny Garkaby, Jessica Willett Pachul, et al. · Pediatric Allergy and Immunology · 2
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A novel variant in RUNX1 in a patient with refractory eosinophilic gastrointestinal disease and long-term clinical response to ketotifen
2022 · Ori Scott, Jenny Garkaby, et al. · LymphoSign Journal · 2
An unusual presentation of DiGeorge syndrome
2022 · Jenny Garkaby, Laura Edith Abrego Fuentes, et al. · LymphoSign Journal · 2
The impact of COVID-19 infection in pediatric and adult patients with primary immunodeficiency: a single center analysis
2023 · Azhar Al Shaqaq, Marina Sham, et al. · LymphoSign Journal · 1
CTLA4 haploinsufficiency caused by a novel heterozygous splice site mutation
2022 · Jenny Garkaby, Laura Edith Abrego Fuentes, et al. · LymphoSign Journal · 1
A Survey-Based Study of Reproductive Health Practices by Immunologists of the Clinical Immunology Society in Patients with Inborn Errors of Immunity
2026 · Jessica Galant-Swafford, Melissa Gans, et al. · Journal of Human Immunity
Corrigendum: A novel variant in RUNX1 in a patient with refractory eosinophilic gastrointestinal disease and long-term clinical response to ketotifen
2023 · Ori Scott, Jenny Garkaby, et al. · LymphoSign Journal
Perspectives of women in science: data sharing in primary immunodeficiency
2023 · Jessica Willett-Pachul · LymphoSign Journal
Case series of COVID-19 outcomes in adult patients with inborn errors of immunity
2022 · Jenny Garkaby, Ori Scott, et al. · LymphoSign Journal
Author response for "DNA‐Binding domain mutations confer severe outcome at an early age among STAT1 gain‐of‐function patients"
2021 · Ori Scott, Harjit Dadi, et al.
Works count: 20
Citation count: 79
H-index: 6
I10-index: 3
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