Dong Li

Also affiliated with China Medical University

Biochemistry, 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 1%percentile

14.7Author 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 →

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

The diploid genome sequence of an Asian individual

Nature(2008)10.1038/nature07484

Top 1%

14.7DataRank

Top 1%964 citations

Wei Wang, Alexandra P. Lewis, Alan Hodgkinson, Geng Tian, Laurie Goodman +75 more

Papers

Driven by 54 papers — median percentile 100. Top paper: “The diploid genome sequence of an Asian individual”.

The diploid genome sequence of an Asian individual

Nature(2008)10.1038/nature07484

Top 1%

14.7DataRank

Top 1%964 citations

Wei Wang, Alexandra P. Lewis, Alan Hodgkinson, Geng Tian, Laurie Goodman +75 more

Common Genetic Variation and Age of Onset of Anorexia Nervosa

Biological Psychiatry Global Open Science(2021)10.1016/j.bpsgos.2021.09.001

N/A

0.726DataRank · unranked

30 citations

Laura M. Thornton, Zeynep Yılmaz, Jessica H. Baker, Jonathan R. I. Coleman, Roger A.H. Adan +95 more

Genome-wide association studies of binge-eating behaviour and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes

medRxiv(2025)10.1101/2025.01.31.25321397

N/A

0.395DataRank · unranked

11 citations

Helena L. Davies, Sang Hyuck Lee, Jessica Dennis, Christopher Hübel, Jessica Johnson +95 more

Kaposiform lymphangiomatosis effectively treated with MEK inhibition

EMBO Molecular Medicine(2020)10.15252/emmm.202012324

N/A

0DataRank · unranked

104 citations

Dong Li, Michael March, Sarah E. Sheppard, Denise M. Adams, Håkon Håkonarson +2 more

Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients

Science Advances(2020)10.1126/sciadv.abc9207

N/A

0DataRank · unranked

99 citations

Dong Li, Samuel G. Cox, Dylan M. Marchione, Evan F. Joiner, Khadija Wilson +95 more

PRKACB variants in skeletal disease or adrenocortical hyperplasia: effects on protein kinase A

Endocrine Related Cancer(2020)10.1530/erc-20-0309

N/A

0DataRank · unranked

19 citations

Ludivine Drougat, Nikolaos Settas, Sara Haydar, Kerstin Bathon, Edra London +8 more

Intragenic Deletions of GNAS in Pseudohypoparathyroidism Type 1A Identify a New Region Affecting Methylation of Exon A/B

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgaa286

N/A

0DataRank · unranked

9 citations

Caleb Bupp, Michael March, Håkon Håkonarson, Michael A. Levine, Dong Li

Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome

Human Molecular Genetics(2020)10.1093/hmg/ddaa050

N/A

0DataRank · unranked

42 citations

Athina Ververi, Ana Beleza‐Meireles, Weizhen Ji, Emily K. Mis, Quinten Patterson +25 more

Activating variants in PDGFRB result in a spectrum of disorders responsive to imatinib monotherapy

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61615

N/A

0DataRank · unranked

35 citations

Randall A. Bly, Natalie Wu, Catherine M. Albert, Julie Park, Joseph T.C. Shieh +26 more

Digenic Heterozygous Mutations in SLC34A3 and SLC34A1 Cause Dominant Hypophosphatemic Rickets with Hypercalciuria

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgaa217

N/A

0DataRank · unranked

30 citations

Dong Li, Daniel Doyle, Joshua J. Zaritsky, Michael A. Levine, Rebecca J. Gordon

Biliary-Atresia-Associated Mannosidase-1-Alpha-2 Gene Regulates Biliary and Ciliary Morphogenesis and Laterality

Frontiers in Physiology(2020)10.3389/fphys.2020.538701

N/A

0DataRank · unranked

26 citations

Mylarappa Ningappa, Joseph Glessner, Jun Min, Chethan Ashokkumar, Sarangarajan Ranganathan +29 more

Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders and known risk factors

medRxiv(2020)10.1101/2020.12.01.20241281

N/A

0DataRank · unranked

29 citations

Jooeun Kang, Adrián I. Campos, Jonathan R. I. Coleman, Alexis C. Edwards, Hanga Galfalvy +95 more

Pathogenic variants in SMARCA5 , a chromatin remodeler, cause a range of syndromic neurodevelopmental features

medRxiv(2020)10.1101/2020.10.26.20217109

N/A

0DataRank · unranked

0 citations

Qin Wang, Naihua N. Gong, Alina Kurolap, Hagit Baris Feldman, Nikolas Boy +33 more

Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62124

N/A

0DataRank · unranked

72 citations

Ian M. Campbell, Margaret Harr, Nina B. Gold, Dong Li, Hans T. Björnsson +95 more

Pathogenic variants in SMARCA5 , a chromatin remodeler, cause a range of syndromic neurodevelopmental features

Science Advances(2021)10.1126/sciadv.abf2066

N/A

0DataRank · unranked

33 citations

Qin Wang, Naihua N. Gong, Alina Kurolap, Hagit Baris Feldman, Nikolas Boy +33 more

ALG13 X‐linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypes

Journal of Inherited Metabolic Disease(2021)10.1002/jimd.12378

N/A

0DataRank · unranked

29 citations

Miao He, Andrew C. Edmondson, Earnest James Paul Daniel, Jie Chen, Tyhiesia Donald +21 more

High-throughput Molecular Analysis of Pseudohypoparathyroidism 1b Patients Reveals Novel Genetic and Epigenetic Defects

The Journal of Clinical Endocrinology & Metabolism(2021)10.1210/clinem/dgab460

N/A

0DataRank · unranked

26 citations

Dong Li, Suzanne M. Jan de Beur, Michael A. Levine, Jennifer A. Danzig

The chromatin remodeler ISWI acts during Drosophila development to regulate adult sleep

Science Advances(2021)10.1126/sciadv.abe2597

N/A

0DataRank · unranked

21 citations

Leela Chakravarti Dilley, Charlette Williams, Emilia H. Moscato, Milán Szuperák, Qin Wang +8 more

Cleft palate morphology, genetic etiology, and risk of mortality in infants with Robin sequence

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62430

N/A

0DataRank · unranked

9 citations

Jonathan A. Perkins, Julia Parish‐Morris, Anne Hing, Maida L. Chen, Christopher M. Cielo︎ +12 more

Molecular identification of bulbospinal ON neurons by GPER, which drives pain and morphine tolerance

Journal of Clinical Investigation(2022)10.1172/jci154588

N/A

0DataRank · unranked

33 citations

Po Gao, Dong Li, Xiaowei Ding, Youqiang Meng, Jiahong Qian +19 more

Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100102

N/A

0DataRank · unranked

26 citations

Laura Bryant, Dong Li, Julie McGaughran, Isabelle Maystadt, Stéphanie Moortgat +34 more

Novel PTH Gene Mutations Causing Isolated Hypoparathyroidism

The Journal of Clinical Endocrinology & Metabolism(2022)10.1210/clinem/dgac086

N/A

0DataRank · unranked

12 citations

Jamal M Al Jubeh, Dong Li, Susan E. Tucker, Tara Rajiyah, Michael A. Levine +1 more

Identification of metabolic pathways underlying FGF1 and CHIR99021-mediated cardioprotection

iScience(2022)10.1016/j.isci.2022.104447

N/A

0DataRank · unranked

10 citations

Fan Li, Wenjing Zhang, Yajuan Su, Ling Tang, Pengsheng Li +9 more

Contribution of Mendelian Disorders in a Population-Based Pediatric Neurodegeneration Cohort

The Journal of Pediatrics(2022)10.1016/j.jpeds.2022.05.017

N/A

0DataRank · unranked

2 citations

Frank Mentch, Dong Li, Erin E. Will, Rebecca C. Ahrens‐Nicklas, Elizabeth Bhoj +1 more

Genome-wide association study meta-analysis of suicide attempt identifies twelve genome-wide significant loci and implicates genetic risks for specific health factors

medRxiv(2022)10.1101/2022.07.03.22277199

N/A

0DataRank · unranked

9 citations

Niamh Mullins, Allison E. Ashley‐Koch, Xuejun Qin, Jonathan R. I. Coleman, Andrey A. Shabalin +95 more

Gain and loss of function variants in EZH1 disrupt neurogenesis timing and cause overlapping neurodevelopmental disorders

medRxiv(2022)10.1101/2022.08.09.22278430

N/A

0DataRank · unranked

1 citations

Yijing Zhou, Qian Yang, Chul‐Hwan Lee, Paula Espana-Bonilla, Shuo Zhang +48 more

GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors

American Journal of Psychiatry(2023)10.1176/appi.ajp.21121266

N/A

0DataRank · unranked

150 citations

Niamh Mullins, Allison E. Ashley‐Koch, Xuejun Qin, Jonathan R. I. Coleman, Andrey A. Shabalin +95 more

Genomic profiling informs diagnoses and treatment in vascular anomalies

Nature Medicine(2023)10.1038/s41591-023-02364-x

N/A

0DataRank · unranked

65 citations

Sarah E. Sheppard, Michael March, Mark R. Battig, Lea F. Surrey, Abhay Srinivasan +37 more

Spliceosome malfunction causes neurodevelopmental disorders with overlapping features

Journal of Clinical Investigation(2023)10.1172/jci171235

N/A

0DataRank · unranked

44 citations

Qin Wang, Allan Bayat, Mark R. Battig, Yijing Zhou, Daniëlle G.M. Bosch +95 more

Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition

JCI Insight(2023)10.1172/jci.insight.155888

N/A

0DataRank · unranked

38 citations

Michael March, Christoph Seiler, Leticia S. Matsuoka, S Kim, Charlly Kao +28 more

Effects of Interleukin-4 (IL-4)-releasing microparticles and adoptive transfer of macrophages on immunomodulation and angiogenesis

Biomaterials(2023)10.1016/j.biomaterials.2023.122095

N/A

0DataRank · unranked

32 citations

Majd Machour, Beatriz Hernaez‐Estrada, Dong Li, Shulamit Levenberg, Kara L. Spiller +1 more

Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes

Journal of Hepatology(2023)10.1016/j.jhep.2023.07.039

N/A

0DataRank · unranked

31 citations

Mylarappa Ningappa, Kim A. Ngo, Maliha Zahid, Juhoon So, Brandon W. Higgs +30 more

Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays

European Journal of Human Genetics(2023)10.1038/s41431-023-01434-5

N/A

0DataRank · unranked

25 citations

Leticia S. Matsuoka, Michael March, Dong Li, Elly Brokamp, Sara Benito‐Sanz +32 more

Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders

Nature Communications(2023)10.1038/s41467-023-39645-5

N/A

0DataRank · unranked

23 citations

Yijing Zhou, Qian Yang, Reza Maroofian, Paula Espana-Bonilla, Chul‐Hwan Lee +95 more

Pathogenic variants inPIK3CAare associated with clinical phenotypes of kaposiform lymphangiomatosis, generalized lymphatic anomaly, and central conducting lymphatic anomaly

Pediatric Blood & Cancer(2023)10.1002/pbc.30419

N/A

0DataRank · unranked

19 citations

Alexandra J. Borst, Sarah E. Sheppard, Kristen Snyder, Dong Li, Lea F. Surrey +10 more

Microcystic lymphatic malformations in Turner syndrome are due to somatic mosaicism of PIK3CA

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63385

N/A

0DataRank · unranked

7 citations

Lydia S. Williams, Niambi Brewer, Lea F. Surrey, Abhay Srinivasan, Dong Li +14 more

Group I metabotropic glutamate receptor-triggered temporally patterned action potential-dependent spontaneous synaptic transmission in mouse MNTB neurons

Hearing Research(2023)10.1016/j.heares.2023.108822

N/A

0DataRank · unranked

2 citations

Kang Peng, Rebecca J. Curry, Dong Li, Yuan Wang, Xiaoyu Wang +2 more

A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63130

N/A

0DataRank · unranked

3 citations

Soumya Rao, Sandra von Hardenberg, Dong Li, Liza L. Cox, Paul C. Lee +34 more

Phage anti-CBASS protein simultaneously sequesters cyclic trinucleotides and dinucleotides

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.01.543220

N/A

0DataRank · unranked

7 citations

Yu Xiao, Erin Huiting, Xujun Cao, Dong Li, Jie Ren +6 more

Single phage proteins sequester TIR- and cGAS-generated signaling molecules

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.15.567273

N/A

0DataRank · unranked

7 citations

Yu Xiao, Weijia Xiong, Iana Fedorova, Yu Wang, Xi Liu +9 more

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition

Research Square(2023)10.21203/rs.3.rs-3317938/v1

N/A

0DataRank · unranked

4 citations

Ghayda Mirzaa, Keqin Yan, Raissa Relator, Sara Timpano, Binnaz Yalcin +57 more

Multiple independent gene disorders causing Bardet--Biedl syndrome, congenital hypothyroidism, and hearing loss in a single Indian consanguineous patient

(2023)10.22541/au.167722036.60770586/v1

N/A

0DataRank · unranked

0 citations

Dong Li, Deborah Watson, Elizabeth M. McCormick, Lisa M. Elden, Thomas Aleman +4 more

Multiple Independent Gene Disorders Causing Bardet–Biedl Syndrome, Congenital Hypothyroidism, and Hearing Loss in a Single Indian Patient

Brain Sciences(2023)10.3390/brainsci13081210

N/A

0DataRank · unranked

0 citations

Dong Li, Deborah Watson, Elizabeth M. McCormick, Lisa M. Elden, T. S. Aleman +4 more

Recurrent small variants in NESP55/NESPAS associated with broad GNAS methylation defects and pseudohypoparathyroidism type 1B

JCI Insight(2024)10.1172/jci.insight.185874

N/A

0DataRank · unranked

4 citations

Suzanne M. Jan de Beur, Cuiping Hou, Maura Ruzhnikov, Hilary Seeley, Garry R. Cutting +3 more

The spectrum of heart defects in the TRAF7 -related multiple congenital anomalies-intellectual disability syndrome

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2317601121

N/A

0DataRank · unranked

4 citations

Chiara De Luca, Francesco Brancati, Rossana Sanchez Russo, Dong Li, Elizabeth Bhoj +29 more

Unusual PHEX variants implicate uncommon genetic mechanisms for X-linked hypophosphatemic rickets

JBMR Plus(2024)10.1093/jbmrpl/ziae152

N/A

0DataRank · unranked

2 citations

Dong Li, Xiang Wang, David R. Weber, Michael A. Levine, Lama Alzoebie

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition

Nature Communications(2025)10.1038/s41467-025-64838-5

N/A

0DataRank · unranked

4 citations

Keqin Yan, Raissa Relator, Mathieu Lévesque, P.S. Jayasinghe, Sara Timpano +61 more

Quantitative hypermorphic FAM111A alleles cause autosomal recessive Kenny-Caffey syndrome type 2 and osteocraniostenosis

JCI Insight(2025)10.1172/jci.insight.186862

N/A

0DataRank · unranked

2 citations

Niels Mailand, Emma Ewing, Saskia Hoffmann, Richard Caswell, Lewis Pang +6 more

Multiple Genomic Technologies Validate Rare Novel Variant and Direct Medical Care in Vascular Anomalies

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64126

N/A

0DataRank · unranked

1 citations

Kristina Woodis, Allison Britt, Lea F. Surrey, Abhay Srinivasan, Arupa Ganguly +6 more

Expansion of the Phenotype of Lymphatic Anomalies Caused by Somatic Activating BRAF Variant

Pediatric Blood & Cancer(2025)10.1002/pbc.32015

N/A

0DataRank · unranked

1 citations

Sumukh Kumar, Allison Britt, Abhay Srinivasan, Lea F. Surrey, Seth Vatsky +7 more

Empowering liver cancer diagnosis and treatment with foundation models: technological innovation and clinical practice

Clinical and Experimental Medicine(2026)10.1007/s10238-025-01980-w

N/A

0DataRank · unranked

0 citations

Siyan Xue, Haoming Xia, Peng Cui, Shizhong Yang, Xiaojuan Wang +8 more

A Pilot Study to Evaluate Neurodevelopmental Outcomes in a Pediatric Cohort With Genodermatoses

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.63989

N/A

0DataRank · unranked

0 citations

Kierstin Keller, Dong Li, Hope Thomas, Nora O’Connor, Abbas F. Jawad +6 more

3D-super-enhancers are condensate-associated cis-regulatory communities

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.02.01.578210

N/A

0DataRank · unranked

0 citations

Kelsey A. Maher, Li Dong, Virginia Valentine, Alaguraj Veluchamy, Li Tian +9 more

De novo MAP2K4 variants cause a novel neurodevelopmental syndrome with impaired JNK signaling in iPSC-derived neurons

medRxiv(2025)10.64898/2025.12.23.25342932

N/A

0DataRank · unranked

0 citations

Alyssa L. Rippert, Sabrina A. Santos De León, Elizabeth M. Gonzalez, Dong Li, Rajesh Angireddy +22 more

Dong Li

Indexed papers

Top data-sharing exemplar

Papers