Peter Nuernberg

Also affiliated with University Hospital Cologne

Biochemistry, 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 14 papers. Top paper: “Large-scale replication and heterogeneity in Parkinson disease genetic loci”.

Large-scale replication and heterogeneity in Parkinson disease genetic loci

Neurology(2012)10.1212/wnl.0b013e318264e353

N/A

6.6DataRank · unranked

132 citations

Grazia Annesi, Alexis Brice, Christine Van Broeckhoven, Muin J. Khoury, Maria Bozi +160 more

Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease

Neurobiology of Aging(2011)10.1016/j.neurobiolaging.2011.05.024

N/A

1.8DataRank · unranked

33 citations

Demetrius M. Maraganore, Peter Nuernberg, Grazia Annesi, Nadine Abahuni, Anna Rita Bentivoglio +42 more

Frequent and Focal FGFR1 Amplification Associates with Therapeutically Tractable FGFR1 Dependency in Squamous Cell Lung Cancer

Science Translational Medicine(2010)10.1126/scitranslmed.3001451

N/A

1.0DataRank · unranked

823 citations

Martin L. Sos, Danila Seidel, Charles M. Perou, Thomas Zander, Johannes M. Heuckmann +66 more

Swarm Learning for decentralized and confidential clinical machine learning

Nature(2021)10.1038/s41586-021-03583-3

N/A

1.0DataRank · unranked

821 citations

Hartmut Schultze, Krishnaprasad Lingadahalli Shastry, Sathyanarayanan Manamohan, Saikat Mukherjee, Vishesh Garg +183 more

Longitudinal Multi-omics Analyses Identify Responses of Megakaryocytes, Erythroid Cells, and Plasmablasts as Hallmarks of Severe COVID-19

Immunity(2020)10.1016/j.immuni.2020.11.017

N/A

0.901DataRank · unranked

405 citations

Neha Mishra, Florian Tran, Thomas Bahmer, Lena Best, Johanna I. Blase +169 more

Community effort to unravel the complex human neuronal landscape exemplified for the striatum

Research Square(2024)10.21203/rs.3.rs-3960911/v1

N/A

0.104DataRank · unranked

1 citations

Shobhit Agrawal, Rebekka Scholz, Celia L. Hartmann, Leon Hetzel, Caterina Carraro +44 more

CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis

Journal of Clinical Investigation(2023)10.1172/jci161156

N/A

0DataRank · unranked

12 citations

Kristof Van Schil, Sandra Liakopoulos, Miriam Bauwens, Alfredo Dueñas Rey, Stephan Käseberg +28 more

Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephaly

Human Genetics(2023)10.1007/s00439-023-02528-2

N/A

0DataRank · unranked

6 citations

Elisabeth Schuler, Almundher Al‐Maawali, Ankur Chaurasia, Steffen Syrbe, Adila Al‐Kindi +10 more

Analysis of 1386 epileptogenic brain lesions reveals association with DYRK1A and EGFR

Nature Communications(2024)10.1038/s41467-024-54911-w

N/A

0DataRank · unranked

22 citations

Costin Leu, Tobias Brünger, Lucas Hoffmann, Sara Baldassari, Mathilde Chipaux +18 more

Genetic contribution to severe COVID-19 in adults under 60 years without major comorbidities in the German National Pandemic Cohort Network (NAPKON)

Human Genomics(2026)10.1186/s40246-025-00904-9

N/A

0DataRank · unranked

0 citations

T. Madhusankha Alawathurage, Axel Schmidt, Fabian Brand, Laura L. Kilarski, Heidi Altmann +45 more

Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects

Brain(2020)10.1093/brain/awaa171

N/A

0DataRank · unranked

81 citations

Eduardo Pérez‐Palma, Daniel P. Howrigan, Yadi Zhou, Feixiong Cheng, Elmo Saarentaus +86 more

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

CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.11.23.469779

N/A

0DataRank · unranked

0 citations

Kristof Van Schil, Sandra Liakopoulos, Miriam Bauwens, Alfredo Dueñas Rey, Stephan Käseberg +28 more

Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita

Research Square(2022)10.21203/rs.3.rs-2121654/v1

N/A

0DataRank · unranked

0 citations

Elisabeth Schuler, Almundher Al‐Maawali, Ankur Chaurasia, Steffen Syrbe, Adila Al‐Kindi +10 more