Deqiong Ma

3.1k total citations
29 papers, 1.3k citations indexed

About

Deqiong Ma is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Deqiong Ma has authored 29 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 9 papers in Molecular Biology and 7 papers in Cognitive Neuroscience. Recurrent topics in Deqiong Ma's work include Genomic variations and chromosomal abnormalities (11 papers), Autism Spectrum Disorder Research (7 papers) and Congenital heart defects research (5 papers). Deqiong Ma is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Autism Spectrum Disorder Research (7 papers) and Congenital heart defects research (5 papers). Deqiong Ma collaborates with scholars based in United States, Australia and Norway. Deqiong Ma's co-authors include Graeme Jones, John R. Gilbert, Michael L. Cuccaro, Jonathan L. Haines, Patrice L. Whitehead, Eden R. Martin, Margaret A. Pericak‐Vance, Ruth K. Abramson, Harry H. Wright and James Jaworski and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Deqiong Ma

26 papers receiving 1.3k citations

Peers

Deqiong Ma

GENET

SURGE

OSM

Margaret Burnett Canada

Fabio Trimarchi Italy

Mona Esbjörnsson Sweden

E. Kirk Neely United States

Maria Kinali United Kingdom

Caroline Brain United Kingdom

Martin J. Somerville Canada

Philip Jardine United Kingdom

Hisataka Kondo Japan

Richard O. Robinson United Kingdom

Margaret Burnett Canada

Deqiong Ma

184 ×0.3

GENET

318 ×0.7

44 ×0.1

140 ×0.6

SURGE

123 ×0.6

OSM

Citations per year, relative to Deqiong Ma Deqiong Ma (= 1×) peers Margaret Burnett

Countries citing papers authored by Deqiong Ma

Since Specialization

Citations

This map shows the geographic impact of Deqiong Ma's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Deqiong Ma with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Deqiong Ma more than expected).

Fields of papers citing papers by Deqiong Ma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deqiong Ma. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Deqiong Ma. The network helps show where Deqiong Ma may publish in the future.

Co-authorship network of co-authors of Deqiong Ma

This figure shows the co-authorship network connecting the top 25 collaborators of Deqiong Ma. A scholar is included among the top collaborators of Deqiong Ma based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Deqiong Ma. Deqiong Ma is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Zafar, Mohammad A., Deqiong Ma, Hui Zhang, et al.. (2024). Somatic Variants Acquired Later in Life Associated with Thoracic Aortic Aneurysms: JAK2 V617F. Genes. 15(7). 883–883.

Velasco, Juan, Yupeng Li, Bulat A. Ziganshin, et al.. (2023). KIF6 Trp719Arg Genetic Variant Increases Risk for Thoracic Aortic Dissection. Genes. 14(2). 252–252. 1 indexed citations

Lebo, Matthew S., Marcie Steeves, Laura K. Conlin, et al.. (2023). O31: Risk allele evidence curation, classification, and reporting: Recommendations from the ClinGen Low Penetrance/Risk Allele Working Group*. SHILAP Revista de lepidopterología. 1(1). 100457–100457. 3 indexed citations

Ma, Deqiong & Bixia Xiang. (2014). Navigating Web-Based Resources for Genetic Testing of Chromosome Abnormalities, CNVs and Gene Mutations. North American Journal of Medicine and Science. 7(4). 1 indexed citations

Ma, Deqiong, et al.. (2013). Biobanking of Residual Specimens from Diagnostic Genetic Laboratories: Standard Operating Procedures, Ethical and Legal Considerations, and Research Applications. North American Journal of Medicine and Science. 6(4). 3 indexed citations

Hedges, Dale J., Kara L. Hamilton‐Nelson, Stephanie Sacharow, et al.. (2012). Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci. Molecular Autism. 3(1). 2–2. 29 indexed citations

Griswold, Anthony J., Deqiong Ma, Holly N. Cukier, et al.. (2012). Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways. Human Molecular Genetics. 21(15). 3513–3523. 143 indexed citations

Cukier, Holly N., Joycelyn M. Lee, Deqiong Ma, et al.. (2012). The Expanding Role of MBD Genes in Autism: Identification of a MECP2 Duplication and Novel Alterations in MBD5, MBD6, and SETDB1. Autism Research. 5(6). 385–397. 68 indexed citations

Hussman, John P., Ren-Hua Chung, Anthony J. Griswold, et al.. (2011). A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism. Molecular Autism. 2(1). 1–1. 171 indexed citations

10.

Yaspan, Brian L., William S. Bush, Eric S. Torstenson, et al.. (2011). Genetic analysis of biological pathway data through genomic randomization. Human Genetics. 129(5). 563–571. 37 indexed citations

11.

Griswold, Anthony J., Deqiong Ma, Stephanie Sacharow, et al.. (2011). A de novo 1.5 Mb microdeletion on chromosome 14q23.2‐23.3 in a patient with autism and spherocytosis. Autism Research. 4(3). 221–227. 24 indexed citations

12.

Cukier, Holly N., Daria Salyakina, Deqiong Ma, et al.. (2011). Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(4). 493–501. 6 indexed citations

13.

Chiquet, Brett, Susan H. Blanton, Amber Burt, et al.. (2008). Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate. Human Molecular Genetics. 17(14). 2212–2218. 144 indexed citations

14.

Collins, Ann L., Deqiong Ma, Patrice L. Whitehead, et al.. (2006). Investigation of autism and GABA receptor subunit genes in multiple ethnic groups. Neurogenetics. 7(3). 167–174. 124 indexed citations

15.

Jones, Graeme, Deqiong Ma, & Fergus Cameron. (2006). Bone Density Interpretation and Relevance in Caucasian Children Aged 9–17 Years of Age: Insights From a Population-Based Fracture Study. Journal of Clinical Densitometry. 9(2). 202–209. 51 indexed citations

16.

Jones, Graeme & Deqiong Ma. (2005). Skeletal age deviation assessed by the Tanner–Whitehouse 2 method is associated with bone mass and fracture risk in children. Bone. 36(2). 352–357. 25 indexed citations

17.

Winzenberg, Tania, et al.. (2005). Synovial haemangioma of the knee: a case report. Clinical Rheumatology. 25(5). 753–755. 17 indexed citations

18.

Mei, Hao, Deqiong Ma, Allison E. Ashley‐Koch, & Eden R. Martin. (2005). Extension of multifactor dimensionality reduction for identifying multilocus effects in the GAW14 simulated data. BMC Genetics. 6(S1). S145–S145. 29 indexed citations

19.

Ma, Deqiong, Ruth Morley, & Graeme Jones. (2004). Risk-taking, coordination and upper limb fractures in children: a population based case-control study. Osteoporosis International. 15(8). 633–8. 34 indexed citations

20.

Jones, Graeme, Changhai Ding, Michael Glisson, et al.. (2003). Knee Articular Cartilage Development in Children: A Longitudinal Study of the Effect of Sex, Growth, Body Composition, and Physical Activity. Pediatric Research. 54(2). 230–236. 106 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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