Yaping Yang

8.1k citations

37 papers · 662 · h-index 16

Impact in

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders

Papers in

Genetics 13
- Genomics and Rare Diseases 9
- Genetics and Neurodevelopmental Disorders 2
- Genomic variations and chromosomal abnormalities 2
- Connective tissue disorders research 2
Molecular Biology 12
- Mitochondrial Function and Pathology 6
- Renal and related cancers 2

Co-authors: Christine M. Eng (13 shared papers)Sarah H. Elsea (4 shared papers)Fernando Scaglia (6 shared papers)James R. Lupski (3 shared papers)Jill A. Rosenfeld (5 shared papers)Richard A. Gibbs (3 shared papers)Christian P. Schaaf (4 shared papers)Matthew N. Bainbridge (2 shared papers)
Journals: Prenatal Diagnosis (2 papers)Genome Medicine (2 papers)Frontiers in Genetics (2 papers)Genetics in Medicine (1 paper)Human Genomics (1 paper)
Partner nations: United States China Hong Kong

In The Last Decade

Yaping Yang

35 papers receiving 656 citations

Peers

Countries citing papers authored by Yaping Yang

Since Specialization

Citations

This map shows the geographic impact of Yaping Yang'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 Yaping Yang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yaping Yang more than expected).

Fields of papers citing papers by Yaping Yang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yaping Yang. 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 Yaping Yang. The network helps show where Yaping Yang may publish in the future.

Co-authors

The 25 scholars most cited alongside Yaping Yang, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Yaping Yang Line = papers co-authored together Yaping Yang links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 37 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Exome sequencing resolves apparent incidental findings and reveals further complexity of SH3TC2 variant alleles causing Charcot-Marie-Tooth neuropathy Genome Medicine ·James R. Lupski, Claudia Gonzaga‐Jauregui, Yaping Yang, Matthew N. Bainbridge, Shalini N. Jhangiani, Christian Buhay, Christie Kovar, Min Wang, Alicia Hawes, Jeffrey G. Reid, Christine M. Eng, Donna M. Muzny, Richard A. Gibbs	2013	74
2	Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformations Nature Genetics ·Xia Wang, Wu‐Lin Charng, Chun‐An Chen, Jill A. Rosenfeld, Aisha Al Shamsi, Lihadh Al‐Gazali, Marianne McGuire, Nicholas Ah Mew, Georgianne L. Arnold, Chunjing Qu, Yan Ding, Donna M. Muzny, Richard A. Gibbs, Christine M. Eng, Magdalena Walkiewicz, Fan Xia, Sharon E. Plon, James R. Lupski, Christian P. Schaaf, Yaping Yang	2017	42
3	Early onset obesity and adrenal insufficiency associated with a homozygous POMC mutation International Journal of Pediatric Endocrinology ·M. Mendiratta, Yaping Yang, Andrea Balázs, Alecia Willis, Christine M. Eng, Lefkothea Karaviti, Lorraine Potocki	2011	36
4	Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice Prenatal Diagnosis ·Lauren Westerfield, Samantha Stover, Veena S. Mathur, Salma Nassef, Tiffiney G. Carter, Yaping Yang, Christine M. Eng, Ignatia B. Van den Veyver	2015	35
5	Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test Referrals Circulation Arrhythmia and Electrophysiology ·Andrew P. Landstrom, Andrew L. Dailey-Schwartz, Jill A. Rosenfeld, Yaping Yang, Margaret J. McLean, Christina Y. Miyake, Santiago O. Valdés, Yuxin Fan, Hugh D. Allen, Daniel J. Penny, Jeffrey J. Kim	2017	35
6	Integrated analysis of metabolomic profiling and exome data supplements sequence variant interpretation, classification, and diagnosis Genetics in Medicine ·Joseph T. Alaimo, Kevin E. Glinton, Ning Liu, Jing Xiao, Yaping Yang, V. Reid Sutton, Sarah H. Elsea	2020	33
7	Improvement of regressive autism symptoms in a child with TMLHE deficiency following carnitine supplementation American Journal of Medical Genetics Part A ·Mark N. Ziats, Mathew S. Comeaux, Yaping Yang, Fernando Scaglia, Sarah H. Elsea, Qin Sun, Arthur L. Beaudet, Christian P. Schaaf	2015	32
8	Reliable detection of subchromosomal deletions and duplications using cell‐based noninvasive prenatal testing Prenatal Diagnosis ·Liesbeth Vossaert, Qun Wang, Roseen Salman, Xinming Zhuo, Chunjing Qu, David Henke, Ron Seubert, Jennifer Chow, Lance U’Ren, Brennan Enright, Jackie L. Stilwell, Eric Kaldjian, Yaping Yang, Chad A. Shaw, Brynn Levy, Ronald J. Wapner, Amy M. Breman, Ignatia Van den Veyver, Arthur L. Beaudet	2018	31
9	Clinical and molecular characterization of de novo loss of function variants in HNRNPU American Journal of Medical Genetics Part A ·Magalie S. Leduc, Hsiao‐Tuan Chao, Chunjing Qu, Magdalena Walkiewicz, Rui Xiao, Pilar Magoulas, Shujuan Pan, Joke Beuten, Weimin He, Jonathan A. Bernstein, Christian P. Schaaf, Fernando Scaglia, Christine M. Eng, Yaping Yang	2017	30
10	Increased diagnostic yield by reanalysis of data from a hearing loss gene panel BMC Medical Genomics ·Yu Sun, Jiale Xiang, Yidong Liu, Sen Chen, Jintao Yu, Jiguang Peng, Zijing Liu, Lisha Chen, Junwei Sun, Yun Yang, Yaping Yang, Yulin Zhou, Zhiyu Peng	2019	25
11	A visual and curatorial approach to clinical variant prioritization and disease gene discovery in genome-wide diagnostics Genome Medicine ·Regis A. James, Ian M. Campbell, Edward S. Chen, Philip M. Boone, Mitchell Rao, Matthew N. Bainbridge, James R. Lupski, Yaping Yang, Christine M. Eng, Jennifer E. Posey, Chad A. Shaw	2016	25
12	Case report and novel treatment of an autosomal recessive Leigh syndrome caused by short‐chain enoyl‐CoA hydratase deficiency American Journal of Medical Genetics Part A ·Brian J. Shayota, Claudia Soler‐Alfonso, Mir Reza Bekheirnia, Elizabeth Mizerik, Suzy W. Boyer, Rui Xiao, Yaping Yang, Sarah H. Elsea, Fernando Scaglia	2019	19
13	Value of Exome Sequencing in Diagnosis and Management of Recurrent Non-immune Hydrops Fetalis: A Retrospective Analysis Frontiers in Genetics ·Xinyao Zhou, Jia Zhou, Xing Wei, Ruen Yao, Yingjun Yang, Linbei Deng, Gang Zou, Xietong Wang, Yaping Yang, Tao Duan, Jian Wang, Luming Sun	2021	18
14	A de novo mutation in the X-linked PAK3 gene is the underlying cause of intellectual disability and macrocephaly in monozygotic twins European Journal of Medical Genetics ·Jozef Hertecant, Makanko Komara, Aslam Nagi, Olfat Al-Zaabi, Waseem Fathallah, Hong Cui, Yaping Yang, Christine M. Eng, Mohammad Al Sorkhy, Mohammad A. Ghattas, Lihadh Al‐Gazali, Bassam R. Ali	2017	18
15	Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review American Journal of Medical Genetics Part A ·Akash Kumar, Diane B. Zastrow, Elijah Kravets, Daniah Beleford, Maura Ruzhnikov, Megan E. Grove, Annika M. Dries, Jennefer N. Kohler, Daryl Waggott, Yaping Yang, Yong Huang, (unknown), Katherine M. Mackenzie, Christine M. Eng, Paul G. Fisher, Euan A. Ashley, Joyce Teng, David A. Stevenson, Joseph T.C. Shieh, Matthew T. Wheeler, Jonathan A. Bernstein	2019	16
16	Incidentally identified genetic variants in arrhythmogenic right ventricular cardiomyopathy‐associated genes among children undergoing exome sequencing reflect healthy population variation Molecular Genetics & Genomic Medicine ·Andrew Headrick, Jill A. Rosenfeld, Yaping Yang, Hari Tunuguntla, Hugh D. Allen, Daniel J. Penny, Jeffrey J. Kim, Andrew P. Landstrom	2019	15
17	Atypical presentation of moyamoya disease in an infant with a de novo RNF213 variant American Journal of Medical Genetics Part A ·Tamar Harel, Jennifer E. Posey, Brett H. Graham, Magdalena Walkiewicz, Yaping Yang, Seema R. Lalani, John W. Belmont	2015	15
18	Homozygous variants in pyrroline‐5‐carboxylate reductase 2 (PYCR2) in patients with progressive microcephaly and hypomyelinating leukodystrophy American Journal of Medical Genetics Part A ·Linyan Meng, Taraka Donti, Fan Xia, Zhiyv Niu, Aisha Al Shamsi, Jozef Hertecant, Fatma Al‐Jasmi, James B. Gibson, Honey Nagakura, Jing Zhang, Weimin He, Christine M. Eng, Yaping Yang, Sarah H. Elsea	2016	15
19	Increased bone turnover, osteoporosis, progressive tibial bowing, fractures, and scoliosis in a patient with a final‐exon SATB2 frameshift mutation American Journal of Medical Genetics Part A ·Philip M. Boone, Yiu Man Chan, Jill V. Hunter, Louis E. Pottkotter, Nelson Davino, Yaping Yang, Joke Beuten, Carlos A. Bacino	2016	15
20	Characterization of the renal phenotype in RMND1‐related mitochondrial disease Molecular Genetics & Genomic Medicine ·Brian J. Shayota, Nhon T. Le, Nasim Bekheirnia, Jill A. Rosenfeld, Amy Goldstein, Michael L. Moritz, Dennis W. Bartholomew, Matthew Pastore, Fan Xia, Christine M. Eng, Yaping Yang, Dolores J. Lamb, Fernando Scaglia, Michael Braun, Mir Reza Bekheirnia	2019	14

About Yaping Yang

Yaping Yang is a scholar working on Genetics, Molecular Biology, Clinical Biochemistry, Neurology and Cardiology and Cardiovascular Medicine, having authored 37 papers that have together received 662 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Mitochondrial Function and Pathology (6 papers), Metabolism and Genetic Disorders (4 papers), Genetics and Neurodevelopmental Disorders (2 papers), Cardiac electrophysiology and arrhythmias (2 papers), Renal and related cancers (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Connective tissue disorders research (2 papers). The work is most often cited by research in Clinical Biochemistry (63 citations), Genetics (251 citations), Endocrine and Autonomic Systems (26 citations), Molecular Biology (277 citations) and Pediatrics, Perinatology and Child Health (69 citations). Yaping Yang has collaborated with scholars based in United States, China and Hong Kong. Frequent co-authors include Christine M. Eng, Sarah H. Elsea, Fernando Scaglia, James R. Lupski, Jill A. Rosenfeld, Richard A. Gibbs, Christian P. Schaaf, Matthew N. Bainbridge, Andrew P. Landstrom and Magdalena Walkiewicz. Their work appears in journals such as Prenatal Diagnosis, Genome Medicine, Frontiers in Genetics, Genetics in Medicine and Human Genomics.

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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Yaping Yang

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Yaping Yang

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About Yaping Yang

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