Yaping Yang

8.0k citations

37 papers · 654 indexed · h-index 16

Co-authors: Christine M. Eng Sarah H. Elsea Fernando Scaglia James R. Lupski Christian P. Schaaf Jill A. Rosenfeld Matthew N. Bainbridge Richard A. Gibbs
Topics: Genomics and Rare Diseases (12 papers)Mitochondrial Function and Pathology (7 papers)Genomic variations and chromosomal abnormalities (6 papers)
Cited by: Clinical Biochemistry Genetics Molecular Biology
Journals: Nature GeneticsSHILAP Revista de lepidopterologíaNeurology
Partner nations: United States China Hong Kong

In The Last Decade

Yaping Yang

35 papers receiving 648 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-authorship network of co-authors of Yaping Yang

This figure shows the co-authorship network connecting the top 25 collaborators of Yaping Yang. A scholar is included among the top collaborators of Yaping Yang 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 Yaping Yang. Yaping Yang 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	CCS MMV may Learn from an UGS Case Implementing Trinity Integrity Risk Management 2025 ·Haiyang Yu,Y. Wang,Jiang Hua,Yaping Yang,Lin Li,Xiaoying Ma	0
2	Early neurological deterioration with severe headache as the initial manifestation: A case report 2024 ·SHILAP Revista de lepidopterología ·M. Tao,Yaping Yang,(unknown),(unknown)	0
3	Case Report: A Novel Homozygous Mutation in MYF5 Due to Paternal Uniparental Isodisomy of Chromosome 12 in a Case of External Ophthalmoplegia With Rib and Vertebral Anomalies 2022 ·Frontiers in Genetics ·Qianqian Li,Xiaofan Zhu,(unknown),(unknown),Ranran Li,Xia Wang,Yaping Yang,Jingjing Meng,Xiangdong Kong	2
4	Familial Autonomic Ganglionopathy Caused by Rare CHRNA3 Genetic Variants 2021 ·Neurology ·Cyndya A. Shibao,Karen M. Joos,John A. Phillips,Joy D. Cogan,John H. Newman,Rizwan Hamid,Jens Meiler,John A. Capra,Jonathan H. Sheehan,Francesco Vetrini,Yaping Yang,Bonnie K. Black,André Diedrich,(unknown),Italo Biaggioni	8
5	Detection of low-level parental somatic mosaicism for clinically relevant SNVs and indels identified in a large exome sequencing dataset 2021 ·Human Genomics ·(unknown),Tomasz Gambin,Roni Zemet,Chung Wah Wu,(unknown),Yaping Yang,Theresa A. Wilson,(unknown),Pengfei Liu,Paweł Stankiewicz	14
6	Value of Exome Sequencing in Diagnosis and Management of Recurrent Non-immune Hydrops Fetalis: A Retrospective Analysis 2021 ·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	18
7	Integrated analysis of metabolomic profiling and exome data supplements sequence variant interpretation, classification, and diagnosis 2020 ·Genetics in Medicine ·Joseph T. Alaimo,Kevin E. Glinton,Ning Liu,Jing Xiao,Yaping Yang,V. Reid Sutton,Sarah H. Elsea	33
8	A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing 2019 ·Journal of Genetic Counseling ·Diane B. Zastrow,Jennefer N. Kohler,Devon Bonner,Chloe M. Reuter,Liliana Fernández,Megan E. Grove,Dianna G. Fisk,(unknown),Yaping Yang,Christine M. Eng,Patricia A. Ward,David Bick,Elizabeth A. Worthey,Paul G. Fisher,Euan A. Ashley,Jonathan A. Bernstein,Matthew T. Wheeler	5
9	Increased diagnostic yield by reanalysis of data from a hearing loss gene panel 2019 ·BMC Medical Genomics ·Yu Sun,Jiale Xiang,(unknown),Sen Chen,Jintao Yu,Jiguang Peng,Zijing Liu,Lisha Chen,Junwei Sun,Yun Yang,Yaping Yang,Yulin Zhou,Zhiyu Peng	22
10	Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review 2019 ·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	16
11	TANGO2-Related Metabolic Encephalopathy and Arrhythmias 2018 ·Seema R. Lalani,Brett H. Graham,Lindsay C. Burrage,Yi‐Chen Lai,Fernando Scaglia,Claudia Soler‐Alfonso,Christina Y. Miyake,Yaping Yang	7
12	Amino acid–level signal-to-noise analysis of incidentally identified variants in genes associated with long QT syndrome during pediatric whole exome sequencing reflects background genetic noise 2018 ·Heart Rhythm ·Andrew P. Landstrom,(unknown),Jill A. Rosenfeld,Yaping Yang,(unknown),Christina Y. Miyake,Hugh D. Allen,Daniel J. Penny,Jeffrey J. Kim	14
13	Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformations 2017 ·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	41
14	A de novo mutation in the X-linked PAK3 gene is the underlying cause of intellectual disability and macrocephaly in monozygotic twins 2017 ·European Journal of Medical Genetics ·Jozef Hertecant,(unknown),(unknown),(unknown),(unknown),Hong Cui,Yaping Yang,Christine M. Eng,(unknown),Mohammad A. Ghattas,Lihadh Al‐Gazali,Bassam R. Ali	18
15	Homozygous variants in pyrroline‐5‐carboxylate reductase 2 (PYCR2) in patients with progressive microcephaly and hypomyelinating leukodystrophy 2016 ·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,(unknown),Jing Zhang,Weimin He,Christine M. Eng,Yaping Yang,Sarah H. Elsea	15
16	Atypical presentation of moyamoya disease in an infant with a de novo RNF213 variant 2015 ·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	15
17	The Expanding MEGDEL Phenotype: Optic Nerve Atrophy, Microcephaly, and Myoclonic Epilepsy in a Child with SERAC1 Mutations 2014 ·JIMD Reports ·Heidi Lumish,Yaping Yang,Fan Xia,Ashley Wilson,Wendy K. Chung	12
18	Clinical Application of Whole-Exome Sequencing 2013 ·JAMA Neurology ·(unknown),Tawfeg Ben‐Omran,Basil T. Darras,Sanjay P. Prabhu,Darryl C. De Vivo,Matteo Vatta,Yaping Yang,Christine M. Eng,Wendy K. Chung	14
19	Exome sequencing resolves apparent incidental findings and reveals further complexity of SH3TC2 variant alleles causing Charcot-Marie-Tooth neuropathy 2013 ·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	74
20	Early onset obesity and adrenal insufficiency associated with a homozygous POMC mutation 2011 ·International Journal of Pediatric Endocrinology ·(unknown),Yaping Yang,(unknown),Alecia Willis,Christine M. Eng,Lefkothea Karaviti,Lorraine Potocki	35

About Yaping Yang

Yaping Yang is a scholar working on Clinical Biochemistry, Genetics and Developmental Biology, having authored 37 papers that have together received 654 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), Mitochondrial Function and Pathology (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). The work is most often cited by research in Clinical Biochemistry (76 citations), Genetics (292 citations) and Molecular Biology (322 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, Christian P. Schaaf, Jill A. Rosenfeld, Matthew N. Bainbridge, Richard A. Gibbs, Magdalena Walkiewicz and Min Wang. Their work appears in journals such as Nature Genetics, SHILAP Revista de lepidopterología and Neurology.

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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