Hongzheng Dai

ScholarGPS® ID: 27547013135626

Affiliation

Baylor College of Medicine, Houston, United States

Affiliation History

Field

Life Sciences

Discipline

Genetics

Top Specialties

Molecular Genetics | Metabolism | Drosophila | Medical Genetics | Birth Defect

Metrics Summary

Publication Count

Predicted Citations

585

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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Novel mutation leading to splice donor loss in a conserved site of DMD gene causes Duchenne muscular dystrophy with cryptorchidism (journal article) Chen, Jianhai \| Jia, Yangying \| Zhong, Jie \| Zhang, Kun \| Dai, Hongzheng \| He, Guanglin \| Li, Fuping \| Zeng, Li \| Fan, Chuanzhu \| Xu, Huayan Journal of Medical Genetics (2024). 10.1136/jmg-2024-109896 Cite \| Source
Prenatal diagnosis of polycystic kidney caused by biallelic hypomorphic variants in the PKD1 gene (journal article) Zheng, Yu \| Wong, Lo \| Kwan, Angel Hoi Wan \| Dong, Zirui \| Kwok, Ka Yin \| Choy, Kwong Wai \| Dai, Hongzheng \| Cao, Ye Prenatal Diagnosis, volume 44, issue 2, pages 247-250 (2024). 10.1002/pd.6419 Cited by (1) \| Cite \| Source
P750: Clinical validation of transcriptome analysis for the diagnosis of Mendelian disorders (journal article) Macakova, Kristina \| Sinson, Jefferson \| Zhao, Sen \| Dai, Hongzheng \| Rosenfeld, Jill \| Zapata, Gladys \| Li, Shenglan \| Ward, Patricia \| Wang, Christiana \| Qu, Chunjing \| ... \| Liu, Pengfei Genetics in Medicine Open, volume 2 (2024). 10.1016/j.gimo.2024.101654 Cite \| Source
P722: Low-level large deletions in mitochondria genomes: A potential diagnosis of mitochondrial diseases (journal article) Yang, Jun \| Chen, Tiansheng \| Kao, Eric \| Dong, Jie \| Lattier, John \| Dai, Hongzheng \| Meng, Linyan \| Xia, Fan \| Schmitt, Eric \| Peacock, Sandra \| ... \| Wang, Yue Genetics in Medicine Open, volume 2 (2024). 10.1016/j.gimo.2024.101626 Cite \| Source
P682: Phenotype expansion or multilocus variants? Additional molecular findings in patients with well-known chromosomal disorders (journal article) Saeidian, Amir Hossein \| Vossaert, Liesbeth \| Mizerik, Elizabeth \| Wu, Wilson CW. \| Dai, Hongzheng \| Owen, Nichole \| Smith, Janice \| Meng, Linyan \| Eng, Christine \| Xia, Fan \| ... \| Zhao, Xiaonan Genetics in Medicine Open, volume 2 (2024). 10.1016/j.gimo.2024.101586 Cite \| Source
P668: PMP22 single exon deletion in a proband with hematologic malignancy and family history of Charcot-Marie-Tooth disease (journal article) Schulze, Katharina \| Kin Chau, Matthew Hoi \| Dai, Hongzheng \| Mizerik, Elizabeth \| Machol, Keren \| Owen, Nichole Genetics in Medicine Open, volume 2 (2024). 10.1016/j.gimo.2024.101573 Cite \| Source
P297: More than an extra chromosome: Unexpected multiple diagnoses in individuals with Down syndrome (journal article) Vossaert, Liesbeth \| Owen, Nichole \| Dai, Hongzheng \| Kao, Eric \| Zhao, Xiaonan \| Lalani, Seema \| Weisz-Hubshman, Monika \| Potocki, Lorraine \| Mizerik, Elizabeth Genetics in Medicine Open, volume 2 (2024). 10.1016/j.gimo.2024.101193 Cite \| Source
P050: Biallelic variants in POLG2 provides a rare molecular diagnosis in a patient with epilepsy and liver failure (journal article) Rossi, Vittoria \| Brooks, Dan \| Dai, Hongzheng \| Mizerik, Elizabeth \| Ben-Moshe, Yishay \| Lalani, Seema \| Scott, Daryl \| Scaglia, Fernando \| Machol, Keren \| Bekheirnia, Mir Reza Genetics in Medicine Open, volume 2 (2024). 10.1016/j.gimo.2024.100927 Cite \| Source
De novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities (journal article) Ward, Scott K. \| Wadley, Alexandrea \| Tsai, Chun‐hui (Anne) \| Benke, Paul J. \| Emrick, Lisa \| Fisher, Kristen \| Houck, Kimberly M. \| Dai, Hongzheng \| Guillen Sacoto, Maria J. \| Craigen, William \| ... \| Rosenfeld, Jill A. American Journal of Medical Genetics Part A, volume 194, issue 1, pages 17-30 (2024). 10.1002/ajmg.a.63399 Cite \| Source
Evaluation of an automated genome interpretation model for rare disease routinely used in a clinical genetic laboratory (journal article) Meng, Linyan \| Attali, Ruben \| Talmy, Tomer \| Regev, Yakir \| Mizrahi, Niv \| Smirin-Yosef, Pola \| Vossaert, Liesbeth \| Taborda, Christian \| Santana, Michael \| Machol, Ido \| ... \| Tzur, Shay Genetics in Medicine, volume 25, issue 6, pages 100830- (2023). 10.1016/j.gim.2023.100830 Cited by (7) \| Cite \| Source
KCNA1 gain‐of‐function epileptic encephalopathy treated with 4‐aminopyridine (journal article) Müller, Peter \| Takacs, Danielle S. \| Hedrich, Ulrike B. S. \| Coorg, Rohini \| Masters, Laura \| Glinton, Kevin E. \| Dai, Hongzheng \| Cokley, Jon A. \| Riviello, James J. \| Lerche, Holger \| Cooper, Edward C. Annals of Clinical and Translational Neurology, volume 10, issue 4, pages 656-663 (2023). 10.1002/acn3.51742 Cited by (11) \| Cite \| Source
Disease modeling of ADAMTS9-related nephropathy using kidney organoids reveals its roles in tubular cells and podocytes (journal article) Yu, Seyoung \| Choi, Yo Jun \| Rim, John Hoon \| Kim, Hye-Youn \| Bekheirnia, Nasim \| Swartz, Sarah Jane \| Dai, Hongzheng \| Gu, Shen Linda \| Lee, Soyeon \| Nishinakamura, Ryuichi \| ... \| Gee, Heon Yung Frontiers in Medicine, volume 10 (2023). 10.3389/fmed.2023.1089159 Cited by (2) \| Cite \| Source
P374: Project GIVE: Expanding genetic testing to underserved areas in the Rio Grande Valley using a telehealth platform (journal article) Brooks, Dan \| Vuocolo, Blake \| Sierra, Roberta \| Holder, Christopher \| Urbanski, Lauren \| Berry, Lori \| Lizardo-Guzman, Segundo \| Hernandez, Ana \| Godoy, Jose Gamez \| Mulukutla, Surya \| ... \| Lalani, Seema Genetics in Medicine Open, volume 1, issue 1, pages 100410- (2023). 10.1016/j.gimo.2023.100410 Cite \| Source
A recurrent single‐exon deletion in TBCK might be under‐recognized in patients with infantile hypotonia and psychomotor delay (journal article) Dai, Hongzheng \| Zhu, Wenmiao \| Yuan, Bo \| Walley, Nicole \| Schoch, Kelly \| Jiang, Yong‐Hui \| Phillips, John A. \| Jones, Melissa S. \| Liu, Pengfei \| Murdock, David R. \| ... \| Xiao, Rui Human Mutation, volume 43, issue 12, pages 1816-1823 (2022). 10.1002/humu.24497 Cited by (1) \| Cite \| Source
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
A novel, de novo intronic variant in POGZ causes White–Sutton syndrome (journal article) Merriweather, Ashanta \| Murdock, David R. \| Rosenfeld, Jill A. \| Dai, Hongzheng \| Ketkar, Shamika \| Emrick, Lisa \| Nicholas, Sarah \| Lewis, Richard A. \| Bacino, Carlos A. \| Scott, Daryl A. \| ... \| Burrage, Lindsay C. American Journal of Medical Genetics Part A, volume 188, issue 7, pages 2198-2203 (2022). 10.1002/ajmg.a.62747 Cited by (3) \| Cite \| Source
PRUNE1 c. 933G >A synonymous variant induces exon 7 skipping, disrupts the DHHA2 domain, and leads to an atypical NMIHBA syndrome presentation: Case report and review of the literature (journal article) Magyar, Christina L. \| Murdock, David R. \| Burrage, Lindsay C. \| Dai, Hongzheng \| Lalani, Seema R. \| Lewis, Richard A. \| Lin, Yuezhen \| Astudillo, Marcela F. \| Rosenfeld, Jill A. \| Tran, Alyssa A. \| ... \| Chao, Hsiao‐Tuan American Journal of Medical Genetics Part A, volume 188, issue 6, pages 1868-1874 (2022). 10.1002/ajmg.a.62704 Cited by (2) \| Cite \| Source
Distinct somatic DICER1 hotspot mutations in three metachronous ovarian Sertoli-Leydig cell tumors in a patient with DICER1 syndrome (journal article) Garcia, Annie \| Desrosiers, Lauren \| Scollon, Sarah \| Gruner, Stephanie \| Reuther, Jacquelyn \| Gandhi, Ilavarasi \| Patil, Ninad \| Fuller, Maren Y. \| Dai, Hongzheng \| Muzny, Donna \| ... \| Roy, Angshumoy Cancer Genetics, volume 262-263 (2022). 10.1016/j.cancergen.2022.01.001 Cited by (2) \| Cite \| Source
eP474: Prenatal exome sequencing analysis in the clinical setting of fetuses with structural anomalies or increased nuchal translucency (journal article) Lazar, Roni Zemet \| Meng, Linyan \| Liu, Pengfei \| Dai, Hongzheng \| Xia, Fan \| Eng, Christine \| Van Den Veyver, Ignatia \| Vossaert, Liesbeth Genetics in Medicine, volume 24, issue 3, pages S301- (2022). 10.1016/j.gim.2022.01.507 Cite \| Source
eP337: Rapid Genome Sequencing (rGS) as first tier test for critically ill children with suspected genetic etiology (journal article) Dai, Hongzheng \| Vossaert, Liesbeth \| Zhao, Xiaonan \| Schulze, Katharina \| Liu, Pengfei \| Qu, Chunjing \| Nguyen, Vy \| Santana, Michael \| Xia, Fan \| Eng, Christine \| Meng, Linyan Genetics in Medicine, volume 24, issue 3, pages S210-S211 (2022). 10.1016/j.gim.2022.01.372 Cite \| Source