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

Tamim H. Shaikh

University of Pennsylvania

ORCID: 0000-0002-4264-4272

Also affiliated with University of Colorado Denver

Biochemistry, Genetics and Molecular BiologyAgricultural and Biological SciencesMedicine

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 4%percentile
0.610Author DataRank

Indexed papers

4in 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 4 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 →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Genome-wide copy number variations in a large cohort of bantu African children

BMC Medical Genomics(2021)10.1186/s12920-021-00978-z
Top 32%
0.610DataRank
Top 32%11 citations

Megan Null, David P. Astling, Hung‐Chun Yu, Joanne B. Cole, Stephanie A. Santorico +6 more

Papers

Driven by 14 papers — median percentile 0. Top paper: “Copy Number Variation Disorders”.

Copy Number Variation Disorders

Current Genetic Medicine Reports(2017)10.1007/s40142-017-0129-2
N/A
3.1DataRank · unranked
94 citations

Tamim H. Shaikh

Microduplications of 16p11.2 are associated with schizophrenia

Nature Genetics(2009)10.1038/ng.474
N/A
0.990DataRank · unranked
733 citations

Kenneth S. Kendler, Manfred Kayser, Anjene M Addington, Jon McClellan, Milica Pejović-Milovančević +66 more

Genome-wide copy number variations in a large cohort of bantu African children

BMC Medical Genomics(2021)10.1186/s12920-021-00978-z
Top 32%
0.610DataRank
Top 32%11 citations

Megan Null, David P. Astling, Hung‐Chun Yu, Joanne B. Cole, Stephanie A. Santorico +6 more

Genome-wide Copy Number Variations in a Large Cohort of Bantu African Children

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.24.424207
N/A
0DataRank · unranked
2 citations

Megan Null, David P. Astling, Hung‐Chun Yu, Joanne B. Cole, Stephanie A. Santorico +6 more

Abnormal expression of GABA A receptor sub-units and hypomotility upon loss of gabra1 in zebrafish

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.31.929455
N/A
0DataRank · unranked
1 citations

Hung‐Chun Yu, Curtis R. Coughlin, Tamim H. Shaikh, Anita M. Quintana, Nayeli G. Reyes‐Nava

22q11.2 Low Copy Repeats Expanded in the Human Lineage

Frontiers in Genetics(2021)10.3389/fgene.2021.706641
N/A
0DataRank · unranked
21 citations

Nicolas Dierckxsens, Zjef Pereboom, Oronzo Capozzi, Mariano Rocchi, Tamim H. Shaikh +2 more

Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation

Genetics(2021)10.1093/genetics/iyaa038
N/A
0DataRank · unranked
20 citations

Feyza Yilmaz, Stephen K. Chow, Catherine Chu, Chin Jia Lin, Elizabeth A. Geiger +7 more

Genome-wide analysis of copy number variants and normal facial variation in a large cohort of Bantu Africans

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100082
N/A
0DataRank · unranked
3 citations

Feyza Yilmaz, David P. Astling, Hung‐Chun Yu, Joanne B. Cole, Benedikt Hallgrímsson +5 more

Multi-modal investigation of the schizophrenia-associated 3q29 genomic interval reveals global genetic diversity with unique haplotypes and segments that increase the risk for non-allelic homologous recombination

medRxiv(2021)10.1101/2021.11.10.21266197
N/A
0DataRank · unranked
2 citations

Gurusamy Umamaheswaran, Trenell J. Mosley, Yulia Mostovoy, Tamim H. Shaikh, Michael E. Zwick +4 more

High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing

Genome Medicine(2023)10.1186/s13073-023-01184-5
N/A
0DataRank · unranked
11 citations

Gurusamy Umamaheswaran, Trenell J. Mosley, Pille Hallast, Kwondo Kim, Yulia Mostovoy +7 more

Data from Genomic Analysis Using High-Density Single Nucleotide Polymorphism-Based Oligonucleotide Arrays and Multiplex Ligation-Dependent Probe Amplification Provides a Comprehensive Analysis of INI1/SMARCB1 in Malignant Rhabdoid Tumors

(2023)10.1158/1078-0432.c.6517843.v1
Top 100%
0DataRank
Top 100%0 citations

Angela J. Sievert, Xiaowu Gai, Håkon Håkonarson, Alexander R. Judkins, Laura Tooke +5 more

Data from Genomic Analysis Using High-Density Single Nucleotide Polymorphism-Based Oligonucleotide Arrays and Multiplex Ligation-Dependent Probe Amplification Provides a Comprehensive Analysis of INI1/SMARCB1 in Malignant Rhabdoid Tumors

(2023)10.1158/1078-0432.c.6517843
Top 100%
0DataRank
Top 100%0 citations

Angela J. Sievert, Xiaowu Gai, Håkon Håkonarson, Alexander R. Judkins, Laura Tooke +5 more

Genome mapping resolves structural variation within segmental duplications associated with microdeletion/microduplication syndromes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.30.071449
N/A
0DataRank · unranked
2 citations

Feyza Yilmaz, Stephen K. Chow, Catherine Chu, Chin Jia Lin, Elizabeth A. Geiger +6 more

The role of Kabuki Syndrome genes KMT2D and KDM6A in development: Analysis in Human sequencing data and compared to mice and zebrafish

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.03.024646
N/A
0DataRank · unranked
4 citations

Ezra Lencer, Elizabeth A. Geiger, Kenneth L. Jones, Tamim H. Shaikh, Kristin Artinger +1 more