Robert Kraaij

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 8 papers. Top paper: “Comparison of Illumina versus Nanopore 16S rRNA Gene Sequencing of the Human Nasal Microbiota”.

Comparison of Illumina versus Nanopore 16S rRNA Gene Sequencing of the Human Nasal Microbiota

Genes(2020)10.3390/genes11091105

N/A

0.723DataRank · unranked

123 citations

Deborah Horst-Kreft, Stefan A. Boers, Rick Jansen, Saskia D. Hiltemann, Willem de Koning +7 more

Comparison of Illumina Versus Nanopore 16S rRNA Gene Sequencing of the Human Nasal Microbiota

10.20944/preprints202008.0677.v1

N/A

0.505DataRank · unranked

28 citations

Deborah Horst-Kreft, Stefan A. Boers, Rick Jansen, Saskia D. Hiltemann, Willem de Koning +7 more

Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors

Human Molecular Genetics(2022)10.1093/hmg/ddac100

N/A

0.434DataRank · unranked

17 citations

Peng Wei, Jennifer A. Brody, Ming‐Huei Chen, Paul S. de Vries, Jennifer E. Huffman +26 more

Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100163

N/A

0.360DataRank · unranked

10 citations

Virginia Fisher, Xuan Deng, Jennifer A. Brody, Misa Graff, Elise Lim +57 more

Exome Sequencing Analysis Identifies Rare Variants in ATM and RPL8 That Are Associated With Shorter Telomere Length

Frontiers in Genetics(2020)10.3389/fgene.2020.00337

N/A

0.330DataRank · unranked

8 citations

Sophie Warner, Linda Broer, Christopher P. Nelson, Dina Vojinović, Shahzad Ahmad +14 more

Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants

UNC Libraries(2024)10.17615/xgme-w279

N/A

0DataRank · unranked

0 citations

Meher Preethi Boorgula, Alison E. Fohner, S.S. Rich, Stella Aslibekyan, Merry‐Lynn McDonald +57 more

Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis

UNC Libraries(2020)10.17615/ayp9-a134

N/A

0DataRank · unranked

0 citations

Nancy E. Lane, Elizabeth Barrett‐Connor, Ana M. Valdes, Floris P. J. G. Lafeber, Kenneth Muir +32 more

Quantifying prion disease penetrance using large population control cohorts

UNC Libraries(2020)10.17615/m8r0-g416

N/A

0DataRank · unranked

1 citations

Hidehiro Mizusawa, Pamela Sklar, Nobuo Sanjo, Miguel Calero, Theo F. J. Kraus +58 more