Weilai Dong

Also affiliated with Hospital of the University of Pennsylvania, Yale University

MedicineImmunology and MicrobiologyBiochemistry, 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 23 papers. Top paper: “A phase 2 evaluation of pembrolizumab for recurrent Lynch‐like versus sporadic endometrial cancers with microsatellite instability”.

A phase 2 evaluation of pembrolizumab for recurrent Lynch‐like versus sporadic endometrial cancers with microsatellite instability

Cancer(2021)10.1002/cncr.34025

N/A

2.4DataRank · unranked

80 citations

Dana M. Roque, Eric R. Siegel, Natália Buza, Pei Hui, Elena Bonazzoli +28 more

A phase II evaluation of pembrolizumab in recurrent microsatellite instability-high (MSI-H) endometrial cancer patients with Lynch-like versus MLH-1 methylated characteristics (NCT02899793)

Annals of Oncology(2021)10.1016/j.annonc.2021.04.013

N/A

1.9DataRank · unranked

50 citations

Dana M. Roque, Eric R. Siegel, Natália Buza, Pei Hui, Elena Bonazzoli +28 more

Integrative modeling of transmitted and de novo variants identifies novel risk genes for congenital heart disease

Quantitative Biology(2021)10.15302/j-qb-021-0248

N/A

0.269DataRank · unranked

5 citations

Xue Zeng, Chentian Jin, Sheng Chih Jin, Weilai Dong, Martina Brueckner +4 more

A Novel Missense Mutation in ERCC8 Co-Segregates with Cerebellar Ataxia in a Consanguineous Pakistani Family

Cells(2022)10.3390/cells11193090

N/A

0.241DataRank · unranked

4 citations

Leon Tejwani, Uzma Abdullah, Sadia Saeed, Shagufta Shafique, Mazhar Badshah +7 more

Uterine leiomyosarcomas harboring MAP2K4 gene amplification are sensitive in vivo to PLX8725, a novel MAP2K4 inhibitor

Gynecologic Oncology(2023)10.1016/j.ygyno.2023.03.009

N/A

0.241DataRank · unranked

4 citations

Justin Harold, Diego Manavella, Stefania Bellone, Levent Mutlu, Tobias M.P. Hartwich +24 more

M-DATA: A Statistical Approach to Jointly Analyzing De Novo Mutations for Multiple Traits

medRxiv(2021)10.1101/2021.05.22.21257421

N/A

0DataRank · unranked

1 citations

Mo Li, Weilai Dong, Wei Jiang, Luca Pinello, Yuhan Xie

Network Assisted Analysis of De Novo Variants Using Protein-Protein Interaction Information Identified 46 Candidate Genes for Congenital Heart Disease

medRxiv(2021)10.1101/2021.11.30.21267069

N/A

0DataRank · unranked

0 citations

Wei Jiang, Weilai Dong, Hongyu Li, Sheng Chih Jin, Martina Brueckner +2 more

Elimusertib (BAY1895344), a novel ATR inhibitor, demonstrates in vivo activity in ATRX mutated models of uterine leiomyosarcoma

Gynecologic Oncology(2022)10.1016/j.ygyno.2022.11.014

N/A

0DataRank · unranked

30 citations

Stefania Bellone, Diego Manavella, Levent Mutlu, Blair McNamara, Tobias M.P. Hartwich +17 more

Mutation spectrum of congenital heart disease in a consanguineous Turkish population

Molecular Genetics & Genomic Medicine(2022)10.1002/mgg3.1944

N/A

0DataRank · unranked

13 citations

Hande Kaymakçalan, Sheng Chih Jin, Nicholas S. Diab, İbrahim Cansaran Tanıdır, Ali Seyfi Yalım Yalçın +7 more

Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia

Journal of Lipid Research(2022)10.1016/j.jlr.2022.100209

N/A

0DataRank · unranked

8 citations

K. Wong, Youbin Liu, Michal Levy‐Sakin, Wei‐Chien Hung, Mo Li +17 more

Network assisted analysis of de novo variants using protein-protein interaction information identified 46 candidate genes for congenital heart disease

PLoS Genetics(2022)10.1371/journal.pgen.1010252

N/A

0DataRank · unranked

8 citations

Wei Jiang, Weilai Dong, Hongyu Li, Sheng Chih Jin, Martina Brueckner +2 more

Non-exercise Machine Learning Models for Maximal Oxygen Uptake Prediction in National Population Surveys

medRxiv(2022)10.1101/2022.09.30.22280471

N/A

0DataRank · unranked

1 citations

Jeph Herrin, Chenxi Huang, Rohan Khera, Lovedeep Singh Dhingra, Weilai Dong +4 more

Multiomic analyses implicate a neurodevelopmental program in the pathogenesis of cerebral arachnoid cysts

Nature Medicine(2023)10.1038/s41591-023-02238-2

N/A

0DataRank · unranked

20 citations

Garrett Allington, Stephen McGee, Kedous Y. Mekbib, Vladimir G. Gainullin, Andrew T. Timberlake +31 more

Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations

Nature Communications(2023)10.1038/s41467-023-43062-z

N/A

0DataRank · unranked

27 citations

Kedous Y. Mekbib, Martijn A. van der Ent, Garrett Allington, Andrew Prendergast, Jocelyn E. Chau +61 more

Nonexercise machine learning models for maximal oxygen uptake prediction in national population surveys

Journal of the American Medical Informatics Association(2023)10.1093/jamia/ocad035

N/A

0DataRank · unranked

5 citations

Jeph Herrin, Chenxi Huang, Rohan Khera, Lovedeep Singh Dhingra, Weilai Dong +4 more

Genetic dysregulation of an endothelial Ras signaling network in vein of Galen malformations

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.03.18.532837

N/A

0DataRank · unranked

3 citations

Kedous Y. Mekbib, Martijn A. van der Ent, Garrett Allington, Andrew Prendergast, Jocelyn E. Chau +58 more

TRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus

Brain(2024)10.1093/brain/awae175

N/A

0DataRank · unranked

21 citations

Bettina Jux, Shujuan Zhao, Kedous Y. Mekbib, Evan Dennis, Weilai Dong +25 more

Exome Sequencing Implicates Impaired GABA Signaling and Neuronal Ion Transport in Trigeminal Neuralgia

iScience(2020)10.1016/j.isci.2020.101552

N/A

0DataRank · unranked

47 citations

Sheng Chih Jin, August Allocco, Xue Zeng, Amar H. Sheth, Shreyas Panchagnula +44 more

Statistical methods for assessing the effects of de novo variants on birth defects

Human Genomics(2024)10.1186/s40246-024-00590-z

N/A

0DataRank · unranked

2 citations

Ruoxuan Wu, Hongyu Li, Weilai Dong, Geyu Zhou, Luca Pinello +1 more

Exome Sequencing as a Potential Diagnostic Adjunct in Sporadic Congenital Hydrocephalus

JAMA Pediatrics(2020)10.1001/jamapediatrics.2020.4878

N/A

0DataRank · unranked

15 citations

Benjamin C. Reeves, Phan Q. Duy, Carol Nelson‐Williams, Weilai Dong, Sheng Chih Jin +2 more

Genetic Defects in DNAH2 Underlie Male Infertility With Multiple Morphological Abnormalities of the Sperm Flagella in Humans and Mice

Frontiers in Cell and Developmental Biology(2021)10.3389/fcell.2021.662903

N/A

0DataRank · unranked

78 citations

Shoaib Nawaz, Jungmin Choi, Huafeng Wang, Shabir Hussain, Mehboob Nawaz +12 more

Analysis workflow to assess de novo genetic variants from human whole-exome sequencing

STAR Protocols(2021)10.1016/j.xpro.2021.100383

N/A

0DataRank · unranked

15 citations

Spencer B. king, Weilai Dong, Garrett Allington, Amar H. Sheth, Samuel T. Peters +3 more

M-DATA: A statistical approach to jointly analyzing de novo mutations for multiple traits

PLoS Genetics(2021)10.1371/journal.pgen.1009849

N/A

0DataRank · unranked

4 citations

Mo Li, Weilai Dong, Wei Jiang, Luca Pinello, Yuhan Xie