🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Ralf Krahe

University of Houston

ORCID: 0000-0002-7810-2539
NeuroscienceBiochemistry, 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 5 papers. Top paper: “Methylation of the candidate biomarker TCF21 is very frequent across a spectrum of early-stage nonsmall cell lung cancers”.

Methylation of the candidate biomarker TCF21 is very frequent across a spectrum of early-stage nonsmall cell lung cancers

UNC Libraries(2020)10.17615/zfd3-9433
N/A
0DataRank · unranked
11 citations

D. Neil Hayes, Wenli Dong, Menghong Sun, Kristy L. Richards, Charmaine D. Wilson +7 more

Confirmation of the Type 2 Myotonic Dystrophy (CCTG)n Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder Effect

UNC Libraries(2020)10.17615/gzep-km85
N/A
0DataRank · unranked
9 citations

Bjarne Udd, Richard T. Moxley, Fred A. Wright, B. Eymard, Armand Bottani +18 more

Pooled Analysis of Loss of Heterozygosity in Breast Cancer: a Genome Scan Provides Comparative Evidence for Multiple Tumor Suppressors and Identifies Novel Candidate Regions

UNC Libraries(2020)10.17615/74e7-pr28
N/A
0DataRank · unranked
0 citations

Brian J. Miller, Ralf Krahe, Fred A. Wright, Daolong Wang

Myotonic dystrophy type 1 (DM1) clinical subtypes and CTCF site methylation status flanking the CTG expansion are mutant allele length-dependent

Human Molecular Genetics(2021)10.1093/hmg/ddab243
N/A
0DataRank · unranked
22 citations

Eyleen Corrales, Baili Zhang, Melissa Vásquez, Carolina Santamaría‐Ulloa, Hazel Quesada +5 more

Osteoblast-Specific Overexpression of Nucleolar Protein NO66/RIOX1 in Mouse Embryos Leads to Osteoporosis in Adult Mice

Journal of Osteoporosis(2023)10.1155/2023/8998556
N/A
0DataRank · unranked
1 citations

Krishna M. Sinha, Benoît De Crombrugghe, Ralf Krahe, Qin Chen