Alexander Hoischen

Also affiliated with Radboud University Medical Center, Radboud Institute for Molecular Life Sciences

Biochemistry, Genetics and Molecular BiologyImmunology and Microbiology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 11 papers. Top paper: “De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa”.

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa

Nature Genetics(2026)10.1038/s41588-025-02451-4

N/A

0.370DataRank · unranked

8 citations

Kim Rodenburg, Zuzana Cvackova, Karolina Kaminska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +212 more

Novel defect in phosphatidylinositol 4‐kinase type 2‐alpha (PI4K2A) at the membrane‐enzyme interface is associated with metabolic cutis laxa

Journal of Inherited Metabolic Disease(2020)10.1002/jimd.12255

N/A

0DataRank · unranked

10 citations

Thatjana Gardeitchik, Shanti Balasubramaniam, Sergio Guerrero‐Castillo, Daisy Dalloyaux, Sanne van Kraaij +16 more

Impact of rare and common genetic variation in the Interleukin-1 pathway on human cytokine responses

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.14.949602

N/A

0DataRank · unranked

2 citations

Peer Arts, Giulio Cavalli, Martin Jaeger, Marloes Steehouwer, Maartje van de Vorst +9 more

Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXAS

Journal of Allergy and Clinical Immunology(2021)10.1016/j.jaci.2021.05.014

N/A

0DataRank · unranked

212 citations

Judith Potjewijd, Annemiek Hoogstins, Huub P J Willems, Arjan J. Kwakernaak, Ruud G.L. de Sévaux +14 more

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

The Journal of Experimental Medicine(2023)10.1084/jem.20221755

N/A

0DataRank · unranked

114 citations

Daniel Leung, Mana Momenilandi, Lauren C.W. Jones, Lucia Pacillo, Alyssa James +89 more

TLR9 ligand sequestration by chemokine CXCL4 negatively affects central B cell tolerance

The Journal of Experimental Medicine(2023)10.1084/jem.20230944

N/A

0DataRank · unranked

16 citations

Marie Dominique Ah Kioon, Yolanda García-Carmona, Salomé Glauzy, David J. Oliver, Natsuko Yamakawa +23 more

“Deficiency in ELF4, X-Linked”: a Monogenic Disease Entity Resembling Behçet’s Syndrome and Inflammatory Bowel Disease

Journal of Clinical Immunology(2024)10.1007/s10875-023-01610-8

N/A

0DataRank · unranked

15 citations

Shannon K. O’Connor, Marat Kribis, Molly L. Bucklin, Dinesh Babu Uthaya Kumar, Paul Tyler +25 more

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa

medRxiv(2025)10.1101/2025.01.06.24317169

N/A

0DataRank · unranked

15 citations

Kim Rodenburg, Zuzana Cvačková, Karolina Kamińska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +95 more

Deciphering the largest disease-associated transcript isoforms in the human neural retina with advanced long-read sequencing approaches

Genome Research(2025)10.1101/gr.280060.124

N/A

0DataRank · unranked

1 citations

Tabea Riepe, Nick Zomer, Renee Salz, Michael Kwint, Jaap Oostrik +15 more

Complexome profiling showed impaired immunoproteasome assembly in a novel PRAAS subtype caused by monoallelic PSMB8 variants

medRxiv(2025)10.1101/2025.06.25.25330124

N/A

0DataRank · unranked

1 citations

Caspar I. van der Made, Sema Kalkan Uçar, Gayatri Ramakrishnan, Jill A. Rosenfeld, Tiphanie P. Vogel +17 more

Long reads decipher genomes and transcriptomes and offer novel insights into biology and diseases

Genome Research(2025)10.1101/gr.280665.125

N/A

0DataRank · unranked

0 citations

Alexander Hoischen, Fritz J. Sedlazeck, Ana Conesa