Carrie L Lucas
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Explore the profile of Carrie L Lucas including associated specialties, affiliations and a list of published articles.
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44
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1658
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Recent Articles
11.
Axisa P, Yoshida T, Lucca L, Kasler H, Lincoln M, Pham G, et al.
Sci Transl Med
. 2022 Dec;
14(675):eabl3651.
PMID: 36516268
Genome-wide association studies identifying hundreds of susceptibility loci for autoimmune diseases indicate that genes active in immune cells predominantly mediate risk. However, identification and functional characterization of causal variants remain...
12.
Al-Ali S, Jeffries L, Faustino E, Ji W, Mis E, Konstantino M, et al.
Am J Med Genet A
. 2022 Jul;
188(10):2869-2878.
PMID: 35899841
The Pediatric Genomics Discovery Program (PGDP) at Yale uses next-generation sequencing (NGS) and translational research to evaluate complex patients with a wide range of phenotypes suspected to have rare genetic...
13.
Hashem H, Bucciol G, Ozen S, Unal S, Bozkaya I, Akarsu N, et al.
J Clin Immunol
. 2022 May;
42(7):1580-1581.
PMID: 35499644
No abstract available.
14.
Lanahan S, Wymann M, Lucas C
Nat Rev Immunol
. 2022 Mar;
22(11):687-700.
PMID: 35322259
Over the past two decades, new insights have positioned phosphoinositide 3-kinase-γ (PI3Kγ) as a context-dependent modulator of immunity and inflammation. Recent advances in protein structure determination and drug development have...
15.
Barmada A, Ramaswamy A, Lucas C
Curr Opin Immunol
. 2021 Oct;
73:50-57.
PMID: 34695727
Monogenic immune disorders provide unprecedented insights into the consequences of disrupting single genes in humans, thereby informing our understanding of fundamental immune function and disease. Genomics has accelerated monogenic disease...
16.
Tyler P, Bucklin M, Zhao M, Maher T, Rice A, Ji W, et al.
Nat Immunol
. 2021 Jul;
22(9):1118-1126.
PMID: 34326534
Transcription factors specialized to limit the destructive potential of inflammatory immune cells remain ill-defined. We discovered loss-of-function variants in the X-linked ETS transcription factor gene ELF4 in multiple unrelated male...
17.
Hashem H, Bucciol G, Ozen S, Unal S, Bozkaya I, Akarsu N, et al.
J Clin Immunol
. 2021 Jul;
41(7):1633-1647.
PMID: 34324127
Purpose: Deficiency of adenosine deaminase 2 (DADA2) is an inherited inborn error of immunity, characterized by autoinflammation (recurrent fever), vasculopathy (livedo racemosa, polyarteritis nodosa, lacunar ischemic strokes, and intracranial hemorrhages),...
18.
Brodsky N, Lucas C
Curr Opin Immunol
. 2021 May;
72:146-157.
PMID: 34052541
Activated PI3K-delta Syndrome (APDS), also called PI3K-delta activating mutation causing senescent T cells, lymphadenopathy, and immunodeficiency (PASLI), is an autosomal dominant disorder caused by inherited or de novo gain-of-function mutations...
19.
Sancho-Shimizu V, Brodin P, Cobat A, Biggs C, Toubiana J, Lucas C, et al.
J Exp Med
. 2021 Apr;
218(6).
PMID: 33904890
Multisystem inflammatory syndrome in children (MIS-C) emerged in April 2020 in communities with high COVID-19 rates. This new condition is heterogenous but resembles Kawasaki disease (KD), a well-known but poorly...
20.
Ramaswamy A, Brodsky N, Sumida T, Comi M, Asashima H, Hoehn K, et al.
Immunity
. 2021 Apr;
54(5):1083-1095.e7.
PMID: 33891889
Multisystem inflammatory syndrome in children (MIS-C) is a life-threatening post-infectious complication occurring unpredictably weeks after mild or asymptomatic SARS-CoV-2 infection. We profiled MIS-C, adult COVID-19, and healthy pediatric and adult...