Weimin Bi

ScholarGPS® ID: 92383705228567

Affiliation

Baylor College of Medicine, Houston, United States

Affiliation History

Field

Life Sciences

Discipline

Genetics

Top Specialties

Metrics Summary

Publication Count

Predicted Citations

8,373

Predicted h-index

Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

Publications
Books
Patents
NIH/NSF

Add Delete
Characterization of atypical IGH rearrangement patterns in plasma cell neoplasms. (journal article) Owen, Nichole \| Bi, Weimin \| Zhao, Xiaonan \| Smith, Janice Journal of Clinical Oncology, volume 42, issue 16_suppl, pages e19525-e19525 (2024). 10.1200/JCO.2024.42.16_suppl.e19525 Cite \| Source
NODAL variants are associated with a continuum of laterality defects from simple D-transposition of the great arteries to heterotaxy (journal article) Dardas, Zain \| Fatih, Jawid M. \| Jolly, Angad \| Dawood, Moez \| Du, Haowei \| Grochowski, Christopher M. \| Jones, Edward G. \| Jhangiani, Shalini N. \| Wehrens, Xander H. T. \| Liu, Pengfei \| ... \| Morris, Shaine A. Genome Medicine, volume 16, issue 1 (2024). 10.1186/s13073-024-01312-9 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
P593: Detection of single-gene copy-number variations through high-resolution exon-targeted chromosomal microarray analysis (journal article) Kin Chau, Matthew Hoi \| Anderson, Stephanie \| Song, Rodger \| Cooper, Lance \| Ward, Patricia \| Yuan, Bo \| Stankiewicz, Pawel \| Cheung, Sau \| Vossaert, Liesbeth \| Wang, Yue \| ... \| Bi, Weimin Genetics in Medicine Open, volume 2 (2024). 10.1016/j.gimo.2024.101499 Cite \| Source
Intrafamilial phenotypic heterogeneity in siblings with pseudohypoparathyroidism 1B due to maternal STX16 deletion (journal article) Odom, John \| Bacino, Carlos A. \| Karaviti, Lefkothea P. \| Bi, Weimin \| Hoyos-Martinez, Alfonso Journal of Pediatric Endocrinology and Metabolism, volume 37, issue 1, pages 84-89 (2024). 10.1515/jpem-2023-0249 Cite \| Source
Expansion of the clinical and molecular spectrum of WWOX ‐related epileptic encephalopathy (journal article) Chong, Shuk Ching \| Cao, Ye \| Fung, Eva L. W. \| Kleppe, Soledad \| Gripp, Karen W. \| Hertecant, Jozef \| El‐Hattab, Ayman W. \| Suleiman, Jehan \| Clark, Gary \| von Allmen, Gretchen \| ... \| Scaglia, Fernando American Journal of Medical Genetics Part A, volume 191, issue 3, pages 776-785 (2023). 10.1002/ajmg.a.63074 Cited by (3) \| Cite \| Source
Compound heterozygosity of a de novo submicroscopic deletion and an inherited frameshift pathogenic variant in the PKHD1 gene in a fetus with bilaterally enlarged and echogenic kidneys, enlarged abdomen and oligohydramnios (journal article) Sakyu, Takuya \| Stover, Samantha R. \| Wang, Yue \| Ward, Patricia \| Gandhi, Manisha \| Braun, Michael C. \| Van den Veyver, Ignatia B. \| Bi, Weimin Clinical Case Reports, volume 11, issue 2 (2023). 10.1002/ccr3.6692 Cite \| Source
P130: Case report: Phenotypic features among four first-degree relatives with 17q11.2 microduplication syndrome (journal article) Bradley, Catherine \| Streff, Haley \| Bi, Weimin \| Smith, Janice \| Rosenfeld, Jill \| Marom, Ronit Genetics in Medicine Open, volume 1, issue 1, pages 100159- (2023). 10.1016/j.gimo.2023.100159 Cite \| Source
Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis (journal article) Kumar, Runjun D. \| Meng, Linyan \| Liu, Pengfei \| Miyake, Christina Y. \| Worley, Kim C. \| Bi, Weimin \| Lalani, Seema R. American Journal of Medical Genetics Part A, volume 188, issue 11, pages 3184-3190 (2022). 10.1002/ajmg.a.62967 Cited by (3) \| 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
LMOD2 ‐related dilated cardiomyopathy presenting in late infancy (journal article) Lay, Erica \| Azamian, Mahshid S. \| Denfield, Susan W. \| Dreyer, William \| Spinner, Joseph A. \| Kearney, Debra \| Zhang, Lilei \| Worley, Kim C. \| Bi, Weimin \| Lalani, Seema R. American Journal of Medical Genetics Part A, volume 188, issue 6, pages 1858-1862 (2022). 10.1002/ajmg.a.62699 Cited by (5) \| Cite \| Source
eP462: Detection of clinically relevant exonic copy number changes in fetuses by chromosomal microarray analysis (journal article) Owen, Nichole \| Okur, Volkan \| Anderson, Stephanie \| Smith, Janice \| Bacino, Carlos \| Ward, Patricia \| Cheung, Sau \| Breman, Amy \| Van Den Veyver, Ignatia \| Bi, Weimin Genetics in Medicine, volume 24, issue 3, pages S291- (2022). 10.1016/j.gim.2022.01.495 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
A rare description of pure partial trisomy of 16q12.2q24.3 and review of the literature (journal article) Manor, Joshua \| Dinu, Daniela \| Azamian, Mahshid S. \| Bi, Weimin \| Darilek, Sandra \| Lalani, Seema R. American Journal of Medical Genetics Part A, volume 185, issue 10, pages 2903-2912 (2021). 10.1002/ajmg.a.62368 Cited by (2) \| Cite \| Source
Clinical characterization of individuals with the distal 1q21.1 microdeletion (journal article) Edwards, Stacey D. \| Schulze, Katharina V. \| Rosenfeld, Jill A. \| Westerfield, Lauren E. \| Gerard, Amanda \| Yuan, Bo \| Grigorenko, Elena L. \| Posey, Jennifer E. \| Bi, Weimin \| Liu, Pengfei American Journal of Medical Genetics Part A, volume 185, issue 5, pages 1388-1398 (2021). 10.1002/ajmg.a.62104 Cited by (5) \| Cite \| Source
Detection of acquired uniparental disomy in clinical exome sequencing of pediatric patients with leukemia predisposition syndromes and its clinical significance (journal article) Zhao, Xiaonan \| Craigen, William \| Owen, Nichole \| Dong, Jie \| Rau, Rachel \| Bi, Weimin \| Dai, Hongzheng Molecular Genetics and Metabolism, volume 132 (2021). 10.1016/S1096-7192(21)00459-5 Cite \| Source
Genetic diagnoses of arthrogryposis by clinical exome or microarray and identification of a new candidate gene: ICE1 (journal article) Owen, Nichole \| Cheng, Hanyin \| Rosenfeld, Jill \| Nassef, Salma \| Singh, Kathryn \| Smith, Janice \| Bacino, Carlos \| Wang, Yue \| Dai, Hongzheng \| Liu, Pengfei \| ... \| Bi, Weimin Molecular Genetics and Metabolism, volume 132 (2021). 10.1016/S1096-7192(21)00393-0 Cite \| Source
Clinical characterization of individuals with the distal 1q21.1 microdeletion (journal article) Edwards, Stacey \| Schulze, Katharina \| Rosenfeld, Jill \| Westerfield, Lauren \| Gerard, Amanda \| Yuan, Bo \| Grigorenko, Elena \| Posey, Jennifer \| Bi, Weimin \| Liu, Pengfei Molecular Genetics and Metabolism, volume 132 (2021). 10.1016/S1096-7192(21)00205-5 Cite \| Source
Integrated sequencing and array comparative genomic hybridization in familial Parkinson disease (journal article) Robak, Laurie A. \| Du, Renqian \| Yuan, Bo \| Gu, Shen \| Alfradique-Dunham, Isabel \| Kondapalli, Vismaya \| Hinojosa, Evelyn \| Stillwell, Amanda \| Young, Emily \| Zhang, Chaofan \| ... \| Shulman, Joshua M. Neurology Genetics, volume 6, issue 5 (2020). 10.1212/NXG.0000000000000498 Cited by (11) \| Cite \| Source
Parental somatic mosaicism for CNV deletions – A need for more sensitive and precise detection methods in clinical diagnostics settings (journal article) Liu, Qian \| Karolak, Justyna A. \| Grochowski, Christopher M. \| Wilson, Theresa A. \| Rosenfeld, Jill A. \| Bacino, Carlos A. \| Lalani, Seema R. \| Patel, Ankita \| Breman, Amy \| Smith, Janice L. \| ... \| Stankiewicz, Pawel Genomics, volume 112, issue 5, pages 2937-2941 (2020). 10.1016/j.ygeno.2020.05.003 Cited by (14) \| Cite \| Source