Deqiong Ma

3.1k citations

29 papers · 1.3k indexed · h-index 18

Co-authors: Graeme Jones John R. Gilbert Michael L. Cuccaro Jonathan L. Haines Patrice L. Whitehead Eden R. Martin Margaret A. Pericak‐Vance Ruth K. Abramson
Topics: Genomic variations and chromosomal abnormalities (11 papers)Autism Spectrum Disorder Research (7 papers)Congenital heart defects research (5 papers)
Cited by: Orthopedics and Sports Medicine Genetics Cognitive Neuroscience
Journals: SHILAP Revista de lepidopterologíaPLoS ONE The Journal of Clinical Endocrinology & Metabolism
Partner nations: United States Australia Norway

In The Last Decade

Deqiong Ma

26 papers receiving 1.3k citations

Peers

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

#	Work	Indexed citations
1	Somatic Variants Acquired Later in Life Associated with Thoracic Aortic Aneurysms: JAK2 V617F 2024 ·Genes ·(unknown),Mohammad A. Zafar,Deqiong Ma,Hui Zhang,Daniel Dykas,Bulat A. Ziganshin,Andreea Popa,Alokkumar Jha,Jennifer M. Kwan,(unknown)	0
2	KIF6 Trp719Arg Genetic Variant Increases Risk for Thoracic Aortic Dissection 2023 ·Genes ·Juan Velasco,Yupeng Li,Bulat A. Ziganshin,Mohammad A. Zafar,John A. Rizzo,Deqiong Ma,(unknown),(unknown),John A. Elefteriades	1
3	O31: Risk allele evidence curation, classification, and reporting: Recommendations from the ClinGen Low Penetrance/Risk Allele Working Group* 2023 ·SHILAP Revista de lepidopterología ·Matthew S. Lebo,Marcie Steeves,(unknown),Laura K. Conlin,Mythily Ganapathi,Vaidehi Jobanputra,Minjie Luo,Deqiong Ma,Kelly McGoldrick,(unknown),Heidi L. Rehm,Panagiotis I. Sergouniotis,Samantha L.P. Schilit,Pınar Bayrak‐Toydemir,Tatiana Tvrdik,N. W. Watkins,(unknown),(unknown),Ryan Schmidt	3
4	Navigating Web-Based Resources for Genetic Testing of Chromosome Abnormalities, CNVs and Gene Mutations 2014 ·North American Journal of Medicine and Science ·Deqiong Ma,Bixia Xiang	1
5	Biobanking of Residual Specimens from Diagnostic Genetic Laboratories: Standard Operating Procedures, Ethical and Legal Considerations, and Research Applications 2013 ·North American Journal of Medicine and Science ·(unknown),(unknown),(unknown),Deqiong Ma,(unknown),Jiansheng Xie,Yu Qi,Peining Li	3
6	Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci 2012 ·Molecular Autism ·Dale J. Hedges,Kara L. Hamilton‐Nelson,Stephanie Sacharow,Laura Nations,Gary W. Beecham,Zhanna Kozhekbaeva,(unknown),Holly N. Cukier,Patrice L. Whitehead,Deqiong Ma,James Jaworski,Lubov Nathanson,Joycelyn M. Lee,Stephen L. Hauser,Jorge R. Oksenberg,Michael L. Cuccaro,Jonathan L. Haines,John R. Gilbert,Margaret A. Pericak‐Vance	29
7	Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways 2012 ·Human Molecular Genetics ·Anthony J. Griswold,Deqiong Ma,Holly N. Cukier,Laura Nations,(unknown),(unknown),James Jaworski,Daria Salyakina,Ioanna Konidari,Patrice L. Whitehead,Harry H. Wright,Ruth K. Abramson,Scott M. Williams,Ramkumar Menon,Eden R. Martin,Jonathan L. Haines,John R. Gilbert,Michael L. Cuccaro,Margaret A. Pericak‐Vance	143
8	The Expanding Role of MBD Genes in Autism: Identification of a MECP2 Duplication and Novel Alterations in MBD5, MBD6, and SETDB1 2012 ·Autism Research ·Holly N. Cukier,Joycelyn M. Lee,Deqiong Ma,Juan I. Young,Vera Mayo,(unknown),(unknown),(unknown),Alexander J. Abrams,Patrice L. Whitehead,Harry H. Wright,Ruth K. Abramson,Jonathan L. Haines,Michael L. Cuccaro,Margaret A. Pericak‐Vance,John R. Gilbert	68
9	A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism 2011 ·Molecular Autism ·John P. Hussman,Ren-Hua Chung,Anthony J. Griswold,James Jaworski,Daria Salyakina,Deqiong Ma,Ioanna Konidari,Patrice L. Whitehead,Jeffery M. Vance,Eden R. Martin,Michael L. Cuccaro,John R. Gilbert,Jonathan L. Haines,Margaret A. Pericak‐Vance	171
10	Genetic analysis of biological pathway data through genomic randomization 2011 ·Human Genetics ·Brian L. Yaspan,William S. Bush,Eric S. Torstenson,Deqiong Ma,Margaret A. Pericak‐Vance,Marylyn D. Ritchie,James S. Sutcliffe,Jonathan L. Haines	37
11	A de novo 1.5 Mb microdeletion on chromosome 14q23.2‐23.3 in a patient with autism and spherocytosis 2011 ·Autism Research ·Anthony J. Griswold,Deqiong Ma,Stephanie Sacharow,(unknown),James Jaworski,Harry H. Wright,Ruth K. Abramson,Helle Lybæk,Nina Øyen,Michael L. Cuccaro,John R. Gilbert,Margaret A. Pericak‐Vance	24
12	Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21 2011 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Holly N. Cukier,Daria Salyakina,(unknown),(unknown),(unknown),Deqiong Ma,Harry H. Wright,Ruth K. Abramson,Ramkumar Menon,Scott M. Williams,Jonathan L. Haines,Michael L. Cuccaro,John R. Gilbert,Margaret A. Pericak‐Vance	6
13	Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate 2008 ·Human Molecular Genetics ·Brett Chiquet,Susan H. Blanton,Amber Burt,Deqiong Ma,Samuel Stal,John B. Mulliken,Jacqueline T. Hecht	144
14	Investigation of autism and GABA receptor subunit genes in multiple ethnic groups 2006 ·Neurogenetics ·Ann L. Collins,Deqiong Ma,Patrice L. Whitehead,Eden R. Martin,Harry H. Wright,Ruth K. Abramson,John P. Hussman,Jonathan L. Haines,Michael L. Cuccaro,John R. Gilbert,Margaret A. Pericak‐Vance	124
15	Bone Density Interpretation and Relevance in Caucasian Children Aged 9–17 Years of Age: Insights From a Population-Based Fracture Study 2006 ·Journal of Clinical Densitometry ·Graeme Jones,Deqiong Ma,Fergus Cameron	51
16	Skeletal age deviation assessed by the Tanner–Whitehouse 2 method is associated with bone mass and fracture risk in children 2005 ·Bone ·Graeme Jones,Deqiong Ma	25
17	Synovial haemangioma of the knee: a case report 2005 ·Clinical Rheumatology ·Tania Winzenberg,Deqiong Ma,(unknown),Andrew Parker,Graeme Jones	17
18	Extension of multifactor dimensionality reduction for identifying multilocus effects in the GAW14 simulated data 2005 ·BMC Genetics ·Hao Mei,Deqiong Ma,Allison E. Ashley‐Koch,Eden R. Martin	29
19	Risk-taking, coordination and upper limb fractures in children: a population based case-control study 2004 ·Osteoporosis International ·Deqiong Ma,Ruth Morley,Graeme Jones	34
20	Knee Articular Cartilage Development in Children: A Longitudinal Study of the Effect of Sex, Growth, Body Composition, and Physical Activity 2003 ·Pediatric Research ·Graeme Jones,Changhai Ding,Michael Glisson,K Hynes,Deqiong Ma,Flavia Cicuttini	106

About Deqiong Ma

Deqiong Ma is a scholar working on Orthopedics and Sports Medicine, Genetics and Internal Medicine, having authored 29 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Autism Spectrum Disorder Research (7 papers) and Congenital heart defects research (5 papers). The work is most often cited by research in Orthopedics and Sports Medicine (221 citations), Genetics (580 citations) and Cognitive Neuroscience (339 citations). Deqiong Ma has collaborated with scholars based in United States, Australia and Norway. Frequent 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. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

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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