Laralynne Przybyla
Overview
Explore the profile of Laralynne Przybyla including associated specialties, affiliations and a list of published articles.
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21
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1119
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Recent Articles
1.
Adli M, Przybyla L, Burdett T, Burridge P, Cacheiro P, Chang H, et al.
Nature
. 2025 Feb;
638(8050):351-359.
PMID: 39939790
Recent advances in functional genomics and human cellular models have substantially enhanced our understanding of the structure and regulation of the human genome. However, our grasp of the molecular functions...
2.
Ge A, Arab A, Dai R, Navickas A, Fish L, Garcia K, et al.
Sci Rep
. 2024 Oct;
14(1):25940.
PMID: 39472491
No abstract available.
3.
Loeb G, Kathail P, Shuai R, Chung R, Grona R, Peddada S, et al.
Nat Genet
. 2024 Sep;
56(10):2078-2092.
PMID: 39256582
Kidney failure, the decrease of kidney function below a threshold necessary to support life, is a major cause of morbidity and mortality. We performed a genome-wide association study (GWAS) of...
4.
Loeb G, Kathail P, Shuai R, Chung R, Grona R, Peddada S, et al.
bioRxiv
. 2024 Jul;
PMID: 38948875
Kidney disease is highly heritable; however, the causal genetic variants, the cell types in which these variants function, and the molecular mechanisms underlying kidney disease remain largely unknown. To identify...
5.
Logan T, Simon M, Rana A, Cherf G, Srivastava A, Davis S, et al.
Cell
. 2024 Mar;
187(6):1565-1566.
PMID: 38490183
No abstract available.
6.
Heo S, Enriquez L, Federman S, Chang A, Mace R, Shevade K, et al.
Genome Biol
. 2024 Jan;
25(1):25.
PMID: 38243310
CRISPR genome editing approaches theoretically enable researchers to define the function of each human gene in specific cell types, but challenges remain to efficiently perform genetic perturbations in relevant models....
7.
Li H, Przybyla L, Blanchard J
Front Cell Dev Biol
. 2024 Jan;
11:1351676.
PMID: 38188018
No abstract available.
8.
Shevade K, Peddada S, Mader K, Przybyla L
Front Cell Dev Biol
. 2023 Aug;
11:1236553.
PMID: 37554308
Protocols to differentiate human pluripotent stem cells have advanced in terms of cell type specificity and tissue-level complexity over the past 2 decades, which has facilitated human disease modeling in...
9.
Przybyla L, Gilbert L
Nat Rev Genet
. 2021 Sep;
23(2):89-103.
PMID: 34545248
The past 25 years of genomics research first revealed which genes are encoded by the human genome and then a detailed catalogue of human genome variation associated with many diseases....
10.
Logan T, Simon M, Rana A, Cherf G, Srivastava A, Davis S, et al.
Cell
. 2021 Aug;
184(18):4651-4668.e25.
PMID: 34450028
GRN mutations cause frontotemporal dementia (GRN-FTD) due to deficiency in progranulin (PGRN), a lysosomal and secreted protein with unclear function. Here, we found that Grn mice exhibit a global deficiency...