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

Zain Awamleh

Hospital for Sick Children

ORCID: 0000-0003-3851-2389

Biochemistry, 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

1in 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 1 indexed paper 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 7 papers. Top paper: “Exposure to Gestational Diabetes Mellitus (GDM) alters DNA methylation in placenta and fetal cord blood”.

Exposure to Gestational Diabetes Mellitus (GDM) alters DNA methylation in placenta and fetal cord blood

Diabetes Research and Clinical Practice(2021)10.1016/j.diabres.2021.108690

N/A

0.612DataRank · unranked

58 citations

Darci T. Butcher, Anthony Hanley, Ravi Retnakaran, Larissa Haertle, Thomas Haaf +3 more

DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes

European Journal of Human Genetics(2022)10.1038/s41431-022-01083-0

N/A

0.510DataRank · unranked

29 citations

Eric Chater‐Diehl, Sanaa Choufani, Elizabeth Y Wei, Rebecca R. Kianmahd, Anna Yu +8 more

Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency

Human Molecular Genetics(2022)10.1093/hmg/ddac098

N/A

0.345DataRank · unranked

9 citations

Anna Lena Burgemeister, Vincent Cantagrel, Jeanne Amiel, Karine Siquier-Pernet, Nathalie Boddaert +16 more

ASXL1 truncating variants in BOS and myeloid leukemia drive shared disruption of Wnt-signaling pathways but have differential isoform usage of RUNX3

BMC Medical Genomics(2024)10.1186/s12920-024-02039-7

N/A

0DataRank · unranked

3 citations

Zain Awamleh, Mili Sinvhal, Andrew C.A. Wan, Leroy Bondhus, Angela Wei +4 more

ASXL1 mutations that cause Bohring Opitz Syndrome (BOS) or acute myeloid leukemia share epigenomic and transcriptomic signatures

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.12.15.519823

N/A

0DataRank · unranked

1 citations

Zain Awamleh, Angela Wei, Bianca Russell, Rosanna Weksberg, Valerie A. Arboleda +1 more

Multi-omics on truncating ASXL1 mutations in Bohring Opitz syndrome identify dysregulation of canonical and non-canonical Wnt signaling

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.12.15.520167

N/A

0DataRank · unranked

3 citations

Angela Wei, Zain Awamleh, Meghna Singh, Aileen Ning, Analeyla Herrera +4 more

Multiomics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and noncanonical Wnt signaling dysregulation

JCI Insight(2023)10.1172/jci.insight.167744

N/A

0DataRank · unranked

13 citations

Angela Wei, Zain Awamleh, Meghna Singh, Aileen Ning, Analeyla Herrera +4 more