Yaping Yang

ScholarGPS® ID: 51071213306859

Affiliation

Baylor College of Medicine, Houston, United States

Affiliation History

Field

Life Sciences

Discipline

Genetics

Top Specialties

Metrics Summary

Publication Count

Predicted Citations

5,202

Predicted h-index

Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

Publications
Books
Patents
NIH/NSF

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Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits (journal article) Yuan, Bo \| Schulze, Katharina V. \| Assia Batzir, Nurit \| Sinson, Jefferson \| Dai, Hongzheng \| Zhu, Wenmiao \| Bocanegra, Francia \| Fong, Chin-To \| Holder, Jimmy \| Nguyen, Joanne \| ... \| Liu, Pengfei Genome Medicine, volume 14, issue 1 (2022). 10.1186/s13073-022-01113-y Cited by (4) \| Cite \| Source
Signal-to-Noise Analysis Can Inform the Likelihood That Incidentally Identified Variants in Sarcomeric Genes Are Associated with Pediatric Cardiomyopathy (journal article) Kurzlechner, Leonie M. \| Jones, Edward G. \| Berkman, Amy M. \| Tadros, Hanna J. \| Rosenfeld, Jill A. \| Yang, Yaping \| Tunuguntla, Hari \| Allen, Hugh D. \| Kim, Jeffrey J. \| Landstrom, Andrew P. Journal of Personalized Medicine, volume 12, issue 5, pages 733- (2022). 10.3390/jpm12050733 Cited by (1) \| Cite \| Source
Detection of low-level parental somatic mosaicism for clinically relevant SNVs and indels identified in a large exome sequencing dataset (journal article) Domogala, Daniel D. \| Gambin, Tomasz \| Zemet, Roni \| Wu, Chung Wah \| Schulze, Katharina V. \| Yang, Yaping \| Wilson, Theresa A. \| Machol, Ido \| Liu, Pengfei \| Stankiewicz, Paweł Human Genomics, volume 15, issue 1 (2021). 10.1186/s40246-021-00369-6 Cited by (12) \| Cite \| Source
Contribution of uniparental disomy in a clinical trio exome cohort of 2675 patients (journal article) Wang, Lei \| Liu, Pengfei \| Bi, Weimin \| Sim, Teresa \| Wang, Xia \| Walkiewicz, Magdalene \| Leduc, Magalie Sophie \| Meng, Linyan \| Xia, Fan \| Eng, Christine M. \| ... \| Dai, Hongzheng Molecular Genetics & Genomic Medicine, volume 9, issue 11 (2021). 10.1002/mgg3.1792 Cited by (3) \| Cite \| Source
Familial Autonomic Ganglionopathy Caused by Rare CHRNA3 Genetic Variants (journal article) Shibao, Cyndya A. \| Joos, Karen \| Phillips, John A. \| Cogan, Joy \| Newman, John H. \| Hamid, Rizwan \| Meiler, Jens \| Capra, John \| Sheehan, Jonathan \| Vetrini, Francesco \| ... \| Biaggioni, Italo Neurology, volume 97, issue 2 (2021). 10.1212/WNL.0000000000012143 Cited by (12) \| Cite \| Source
Heterozygous variants in SPTBN1 cause intellectual disability and autism (journal article) Rosenfeld, Jill A. \| Xiao, Rui \| Bekheirnia, Mir Reza \| Kanani, Farah \| Parker, Michael J. \| Koenig, Mary K. \| van Haeringen, Arie \| Ruivenkamp, Claudia \| Rosmaninho‐Salgado, Joana \| Almeida, Pedro M. \| ... \| Lee, Brendan H. American Journal of Medical Genetics Part A, volume 185, issue 7, pages 2037-2045 (2021). 10.1002/ajmg.a.62201 Cited by (10) \| Cite \| Source
Genotype‐phenotype study and expansion of ARL6IP1 ‐related complicated hereditary spastic paraplegia (journal article) Cao, Ye \| Manning, Melanie \| Pope, Kathleen \| He, Weimin \| Vetrini, Francesco \| Siskind, Carly \| Rosenfeld, Jill A. \| Yang, Yaping \| Xiao, Rui Clinical Genetics, volume 99, issue 3, pages 477-480 (2021). 10.1111/cge.13870 Cited by (3) \| Cite \| Source
The expanding clinical phenotype of germline ABL1 ‐associated congenital heart defects and skeletal malformations syndrome (journal article) Chen, Chun‐An \| Crutcher, Emeline \| Gill, Harinder \| Nelson, Tanya N. \| Robak, Laurie A. \| Jongmans, Marjolijn C. J. \| Pfundt, Rolph \| Prasad, Chitra \| Berard, Roberta A. \| Fannemel, Madeleine \| ... \| Wang, Xia Human Mutation, volume 41, issue 10, pages 1738-1744 (2020). 10.1002/humu.24075 Cited by (13) \| Cite \| Source
Integrated analysis of metabolomic profiling and exome data supplements sequence variant interpretation, classification, and diagnosis (journal article) Alaimo, Joseph T. \| Glinton, Kevin E. \| Liu, Ning \| Xiao, Jing \| Yang, Yaping \| Reid Sutton, V. \| Elsea, Sarah H. Genetics in Medicine, volume 22, issue 9, pages 1560-1566 (2020). 10.1038/s41436-020-0827-0 Cited by (33) \| Cite \| Source
Wolff–Parkinson–White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation (journal article) Coban‐Akdemir, Zeynep H. \| Charng, Wu‐Lin \| Azamian, Mahshid \| Paine, Ingrid S. \| Punetha, Jaya \| Grochowski, Christopher M. \| Gambin, Tomasz \| Valdes, Santiago O. \| Cannon, Bryan \| Zapata, Gladys \| ... \| Lalani, Seema R. American Journal of Medical Genetics Part A, volume 182, issue 6, pages 1387-1399 (2020). 10.1002/ajmg.a.61571 Cited by (19) \| Cite \| Source
BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder (journal article) Scott, Tiana M. \| Guo, Hui \| Eichler, Evan E. \| Rosenfeld, Jill A. \| Pang, Kaifang \| Liu, Zhandong \| Lalani, Seema \| Bi, Weimin \| Yang, Yaping \| Bacino, Carlos A. \| ... \| Scott, Daryl A. Human Mutation, volume 41, issue 5, pages 921-925 (2020). 10.1002/humu.23992 Cited by (11) \| Cite \| Source
Further delineation of the phenotypic spectrum associated with hemizygous loss‐of‐function variants in NONO (journal article) Sewani, Maham \| Nugent, Kimberly \| Blackburn, Patrick R. \| Tarnowski, Jessica M. \| Hernandez‐Garcia, Andres \| Amiel, Jeanne \| Whalen, Sandra \| Keren, Boris \| Courtin, Thomas \| Rosenfeld, Jill A. \| ... \| Scott, Daryl A. American Journal of Medical Genetics Part A, volume 182, issue 4, pages 652-658 (2020). 10.1002/ajmg.a.61466 Cited by (15) \| Cite \| Source
Novel Missense Variants in ADAT3 as a Cause of Syndromic Intellectual Disability (journal article) Thomas, Elizabeth \| Lewis, Andrea M. \| Yang, Yaping \| Chanprasert, Sirisak \| Potocki, Lorraine \| Scott, Daryl A. Journal of Pediatric Genetics, volume 08, issue 04, pages 244-251 (2019). 10.1055/s-0039-1693151 Cited by (10) \| Cite \| Source
Characterization of the renal phenotype in RMND1 ‐related mitochondrial disease (journal article) Shayota, Brian J. \| Le, Nhon T. \| Bekheirnia, Nasim \| Rosenfeld, Jill A. \| Goldstein, Amy C. \| Moritz, Michael \| Bartholomew, Dennis W. \| Pastore, Matthew T. \| Xia, Fan \| Eng, Christine \| ... \| Bekheirnia, Mir Reza Molecular Genetics & Genomic Medicine, volume 7, issue 12 (2019). 10.1002/mgg3.973 Cited by (10) \| Cite \| Source
Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing (journal article) Reuter, Chloe M. \| Kohler, Jennefer N. \| Bonner, Devon \| Zastrow, Diane \| Fernandez, Liliana \| Dries, Annika \| Marwaha, Shruti \| Davidson, Jean \| Brokamp, Elly \| Herzog, Matthew \| ... \| Wheeler, Matthew T. Journal of Genetic Counseling, volume 28, issue 6, pages 1107-1118 (2019). 10.1002/jgc4.1161 Cited by (42) \| Cite \| Source
A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing (journal article) Cao, Ye \| Tokita, Mari J. \| Chen, Edward S. \| Ghosh, Rajarshi \| Chen, Tiansheng \| Feng, Yanming \| Gorman, Elizabeth \| Gibellini, Federica \| Ward, Patricia A. \| Braxton, Alicia \| ... \| Stankiewicz, Pawel Genome Medicine, volume 11, issue 1 (2019). 10.1186/s13073-019-0658-2 Cited by (46) \| Cite \| Source
DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract (journal article) Blackburn, Alexandria T.M. \| Bekheirnia, Nasim \| Uma, Vanessa C. \| Corkins, Mark E. \| Xu, Yuxiao \| Rosenfeld, Jill A. \| Bainbridge, Matthew N. \| Yang, Yaping \| Liu, Pengfei \| Madan-Khetarpal, Suneeta \| ... \| Bekheirnia, Mir Reza Genetics in Medicine, volume 21, issue 12, pages 2755-2764 (2019). 10.1038/s41436-019-0576-0 Cited by (18) \| Cite \| Source
Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review (journal article) Kumar, Akash \| Zastrow, Diane B. \| Kravets, Elijah J. \| Beleford, Daniah \| Ruzhnikov, Maura R. Z. \| Grove, Megan E. \| Dries, Annika M. \| Kohler, Jennefer N. \| Waggott, Daryl M. \| Yang, Yaping \| ... \| Bernstein, Jonathan A. American Journal of Medical Genetics Part A, volume 179, issue 6, pages 966-977 (2019). 10.1002/ajmg.a.61134 Cited by (20) \| Cite \| Source
Incidentally identified genetic variants in arrhythmogenic right ventricular cardiomyopathy‐associated genes among children undergoing exome sequencing reflect healthy population variation (journal article) Headrick, Andrew T. \| Rosenfeld, Jill A. \| Yang, Yaping \| Tunuguntla, Hari \| Allen, Hugh D. \| Penny, Daniel J. \| Kim, Jeffrey J. \| Landstrom, Andrew P. Molecular Genetics & Genomic Medicine, volume 7, issue 6 (2019). 10.1002/mgg3.593 Cited by (11) \| Cite \| Source
Case report and novel treatment of an autosomal recessive Leigh syndrome caused by short‐chain enoyl‐CoA hydratase deficiency (journal article) Shayota, Brian J. \| Soler‐Alfonso, Claudia \| Bekheirnia, Mir Reza \| Mizerik, Elizabeth \| Boyer, Suzy W. \| Xiao, Rui \| Yang, Yaping \| Elsea, Sarah H. \| Scaglia, Fernando American Journal of Medical Genetics Part A, volume 179, issue 5, pages 803-807 (2019). 10.1002/ajmg.a.61074 Cited by (18) \| Cite \| Source