Profil bibliographique

Gundula Povysil

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

67Publications signalées

2584Citations signalées

3Affiliations récentes

Institutions déclarées

Bridgepoint (United States)New York Genome Center Columbia University

Domaines associés

Genomics and Rare DiseasesGenetic Associations and Epidemiologyinterferon and immune responsesRenal and related cancersGenomics and Phylogenetic Studies

Publications récentes

Accès ouvert 2025 conference-abstractOpenAlex

240 WAY-102: an in vivo lentiviral dual-armored CLDN18.2 CAR T engineered for long-term durability & cytotoxicity in the tumor microenvironment

Cassandra Kontur, Reeti Sanghrajka, Liang He, Gundula Povysil et autres

0 citationsRegular and Young Investigator Award Abstracts

Accès ouvert 2025 erratumOpenAlex

Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes

Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, Gundula Povysil et autres

0 citationsNature Communications

Accès ouvert 2025 erratumOpenAlex

Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes

Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, Gundula Povysil et autres

0 citationsUtrecht University Repository (Utrecht University)

2025 articleOpenAlex

Analysis of the Coding Regions of 33,894 Individuals Identifies Known and Novel Gene Associations for Idiopathic Nephrotic Syndrome

Juntao Ke, Gundula Povysil, Shirlee Shril, Yask Gupta et autres

0 citationsJournal of the American Society of Nephrology

2025 articleOpenAlex

Genome-Wide Association Study for Idiopathic Nephrotic Syndrome Identifies Susceptibility Loci Across the Lifespan, Response to Therapy, and Genetic Ancestry

Tze Yin Lim, Yask Gupta, Juntao Ke, Michelle T. McNulty et autres

0 citationsJournal of the American Society of Nephrology

Accès ouvert 2025 articleOpenAlex

Exome analysis links kidney malformations to developmental disorders and reveals causal genes

Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, Gundula Povysil et autres

10 citationsNature Communications

Accès ouvert 2025 articleOpenAlex

Exome analysis links kidney malformations to developmental disorders and reveals causal genes

Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, Gundula Povysil et autres

0 citationsUtrecht University Repository (Utrecht University)

2025 conference-abstractOpenAlex

Abstract 3181: Single cell characterization and anti-tumor efficacy of single & multi-armored CAR Ts against CLDN18.2

Megha Sah, Liang He, Gundula Povysil, Cassandra Kontur et autres

0 citationsCancer Research

Accès ouvert 2024 preprintOpenAlex

Exome-wide analysis of congenital kidney anomalies reveals new genes and shared architecture with developmental disorders

Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, Gundula Povysil et autres

1 citationmedRxiv

Accès ouvert 2024 conference-abstractOpenAlex

330 Pooled in vivo screens using spatial biology identify CAR T designs with superior performance in pancreatic cancer

Megha Sah, A.-H. Kwon, Mariya London, Liang He et autres

1 citationRegular and Young Investigator Award Abstracts

Accès ouvert 2024 articleOpenAlex

Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLS

Tess D. Pottinger, Joshua E. Motelow, Gundula Povysil, Cristiane Araújo Martins Moreno et autres

5 citationsBMC Genomics

2024 conference-abstractOpenAlex

Abstract 6329: Pooled in vivo screening of hundreds of T cell therapy designs using spatial multi-omics identifies novel designs with superior TME performance

Cassandra Kontur, Gundula Povysil, Megha Sah, Mariya London et autres

0 citationsCancer Research

Profil ORCID Notice OpenAlex

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