Bodo B. Beck

Also affiliated with University Hospital Cologne

MedicineBiochemistry, Genetics and Molecular Biology

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 6 papers. Top paper: “cfNOMe — A single assay for comprehensive epigenetic analyses of cell-free DNA”.

cfNOMe — A single assay for comprehensive epigenetic analyses of cell-free DNA

Genome Medicine(2020)10.1186/s13073-020-00750-5

N/A

0DataRank · unranked

71 citations

Deborah Nörling, Domenica Borchert, Esther Leenen, Sandra Habbig, Michael S. Wiesener +8 more

An international cohort study of autosomal dominant tubulointerstitial kidney disease due to mutations identifies distinct clinical subtypes

Kidney International(2020)10.1016/j.kint.2020.06.041

N/A

0DataRank · unranked

43 citations

Kendrah Kidd, Mohamad Zaidan, Petr Vyleťal, Veronika Barešová, Kateřina Hodaňová +51 more

De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.01.008

N/A

0DataRank · unranked

27 citations

Amar J. Majmundar, Kamal Khan, Tze Yin Lim, Shirlee Shril, Gina Jin +62 more

NPHP1 gene-associated nephronophthisis is associated with an occult retinopathy

Kidney International(2021)10.1016/j.kint.2021.06.012

N/A

0DataRank · unranked

9 citations

Georg Spital, Marius Book, Sandra Habbig, Sören Bäumner, Vera Riehmer +8 more

C1GALT1C1 ‐Associated Mosaic Disorder of Glycosylation in a Female

Journal of Inherited Metabolic Disease(2025)10.1002/jimd.70006

N/A

0DataRank · unranked

1 citations

Aditya Ramanujan, Camille Bucci, Christian Neckelmann, Jamie Heimburg‐Molinaro, Sandra F. Cummings +5 more

Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatment

Nature Communications(2025)10.1038/s41467-025-65663-6

N/A

0DataRank · unranked

0 citations

Daanya Salmanullah, Lorrin Liang, Victoria C. Gauntner, Kavita Krueger, Jiansong Qi +31 more