Jesmeen Maimaris - Concepedia

Author

Jesmeen Maimaris

Also Known As

Bella Madan, Dragana Josifova, Genevieve Sayer, Hana Lango Allen, Hilary Longhurst, J Maimaris, J. Maimaris, Jennifer Martin, Jenny Carmichael, Jesmeen Maimaris

Publications

Citations

H-Index

Concepts

All Affiliations

University College London Great Ormond Street Hospital University of Cambridge Royal Free London NHS Foundation Trust NHS Blood and Transplant

About

Jesmeen Maimaris is an author at University College London specializing in medicine, genetics, and molecular diagnostics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	6	956
2	Pathology	4	5	836
3	Immunology	3	4	423
4	Molecular Genetics	2	2	583
5	Allergy	1	2	76

Jesmeen Maimaris

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease Keren Carss, Gavin Arno, Marie Erwood, The American Journal of Human Genetics Whole-genome SequencingAllelic VariantGenetic DisorderMedicineGenetics	2016	463
Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans Paul Tuijnenburg, Hana Lango Allen, Siobhan O. Burns, Journal of Allergy and Clinical Immunology Primary ImmunodeficiencyDisease SusceptibilityImmune Cell DevelopmentGeneticsImmunodeficiencies	2018	227
Thymus transplantation for complete DiGeorge syndrome: European experience E. Graham Davies, Melissa Cheung, Kimberly Gilmour, Journal of Allergy and Clinical Immunology	2017	132
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations Tiziana Lorenzini, Manfred Fliegauf, Nils Klammer, Journal of Allergy and Clinical Immunology Autoimmune DiseaseGenetic DisorderMedicineGeneticsImmunologic Phenotype	2020	120
Human germline heterozygous gain-of-function <i>STAT6</i> variants cause severe allergic disease Mehul Sharma, Daniel Leung, Mana Momenilandi, The Journal of Experimental Medicine	2023	99
Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes James Whitworth, Philip Smith, Jose‐Ezequiel Martín, The American Journal of Human Genetics Tumor BiologySomatic VariantBroad RangeTumor HeterogeneityAtypical Tumor Phenotypes	2018	70
Bayesian Inference Associates Rare <i>KDR</i> Variants With Specific Phenotypes in Pulmonary Arterial Hypertension Emilia M. Swietlik, Daniel Greene, Na Zhu, Circulation Genomic and Precision Medicine	2020	44
Autosomal Dominant STAT6 Gain of Function Causes Severe Atopy Associated with Lymphoma Ekaterina Minskaia, Jesmeen Maimaris, Persephone Jenkins, Journal of Clinical Immunology Transcription Factor Stat6ImmunologyPathologyDermatologyImmunotherapy	2023	38
Whole genome sequencing of a sporadic primary immunodeficiency cohort James Thaventhiran, Hana Lango Allen, Oliver S. Burren,	2018	22
Biallelic deleterious germline <i>SH2B3</i> variants cause a novel syndrome of myeloproliferation and multi‐organ autoimmunity Piers Blombery, Vahid Pazhakh, Adriana S. Albuquerque, eJHaem	2023	20

Page 1