Jan Halbritter

Also affiliated with Charité - Universitätsmedizin Berlin

Biochemistry, Genetics and Molecular BiologyMedicine

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 10 papers. Top paper: “Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference”.

Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

Kidney International(2022)10.1016/j.kint.2022.03.019

N/A

4.5DataRank · unranked

193 citations

Émilie Cornec-Le Gall, Jan Halbritter, Krzysztof Kiryluk, Andrew Mallett, Rulan S. Parekh +57 more

Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity, confirming the gene’s candidacy in 6q16.1 deletions

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.04.010

N/A

0.430DataRank · unranked

9 citations

Wenjun Jin, Christin Findeisen, Irene Valenzuela, Laura A. Devlin, Jill R. Murrell +35 more

ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6

UNC Libraries(2020)10.17615/60dd-hv24

N/A

0DataRank · unranked

0 citations

Dalal A. Al-Mutairi, Rim Hjeij, Margaret W. Leigh, Stefan Kohl, Lucy Morgan +27 more

Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia

UNC Libraries(2020)10.17615/n407-9288

N/A

0DataRank · unranked

0 citations

Stephanie D. Davis, Yan Liu, Raqual Bower, Nathan E. Hellman, Douglas Tritschler +27 more

KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease

European Journal of Human Genetics(2023)10.1038/s41431-023-01296-x

N/A

0DataRank · unranked

14 citations

Laura R. Claus, Henry H. Wiersma, Roy Oelen, Floor Schukking, Niek de Klein +16 more

Disrupted uromodulin trafficking is rescued by targeting TMED cargo receptors

Journal of Clinical Investigation(2024)10.1172/jci180347

N/A

0DataRank · unranked

16 citations

Matthew Brown, Jason Zavras, Magdalena Riedl Khursigara, Elizabeth Grinkevich, Eriene-Heidi Sidhom +29 more

Pathogenic PHIP Variants are Variably Associated With CAKUT

Kidney International Reports(2024)10.1016/j.ekir.2024.05.024

N/A

0DataRank · unranked

8 citations

Tobias Sieckmann, Ria Schönauer, Friederike Petzold, Johannes Münch, M. Pauly +15 more

Novel nephronophthisis-associated variants reveal functional importance of MAPKBP1 dimerization for centriolar recruitment

Kidney International(2020)10.1016/j.kint.2020.05.027

N/A

0DataRank · unranked

12 citations

Wenjun Jin, Anastasia Ertel, Melanie Nemitz‐Kliemchen, Nydia Panitz, Elena Hantmann +12 more

The impact of a secondary, rare, non-pathogenic PKD1 variant on disease progression in autosomal dominant polycystic kidney disease

Journal of Nephrology(2025)10.1007/s40620-025-02211-x

N/A

0DataRank · unranked

0 citations

Kane E. Collins, Sophia Heneghan, Edmund Gilbert, Hana Yang, Sarah R. Senum +82 more

Mutations in SPAG1 Cause Primary Ciliary Dyskinesia Associated with Defective Outer and Inner Dynein Arms

UNC Libraries(2020)10.17615/2mgm-cp36

N/A

0DataRank · unranked

0 citations

Johanna Raidt, Charlotte Jahnke, Gerard W. Dougherty, Rim Hjeij, Claudius Werner +27 more