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Stella Maris Chen
Stella Maris Chen
Baylor Genetics
Verified email at baylorgenetics.com
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Cited by
Year
Biparental inheritance of mitochondrial DNA in humans
S Luo, CA Valencia, J Zhang, NC Lee, J Slone, B Gui, X Wang, Z Li, ...
Proceedings of the National Academy of Sciences 115 (51), 13039-13044, 2018
3772018
Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA
J Zhang, J Li, JB Saucier, Y Feng, Y Jiang, J Sinson, AK McCombs, ...
Nature medicine 25 (3), 439-447, 2019
1542019
Characterizing regulatory and functional differentiation between maize mesophyll and bundle sheath cells by transcriptomic analysis
YM Chang, WY Liu, ACC Shih, MN Shen, CH Lu, MYJ Lu, HW Yang, ...
Plant physiology 160 (1), 165-177, 2012
1492012
A comprehensive strategy for accurate mutation detection of the highly homologous PMS2
J Li, H Dai, Y Feng, J Tang, S Chen, X Tian, E Gorman, ES Schmitt, ...
The Journal of Molecular Diagnostics 17 (5), 545-553, 2015
462015
Transcriptomes of mouse olfactory epithelium reveal sexual differences in odorant detection
MS Shiao, AYF Chang, BY Liao, YH Ching, MYJ Lu, SM Chen, WH Li
Genome biology and evolution 4 (5), 703-712, 2012
462012
De novo missense variants in TRAF7 cause developmental delay, congenital anomalies, and dysmorphic features
MJ Tokita, CA Chen, D Chitayat, E Macnamara, JA Rosenfeld, ...
The American Journal of Human Genetics 103 (1), 154-162, 2018
302018
Added value of next generation gene panel analysis for patients with elevated methylmalonic acid and no clinical diagnosis following functional studies of vitamin B12 metabolism
M Pupavac, X Tian, J Chu, G Wang, Y Feng, S Chen, R Fenter, VW Zhang, ...
Molecular genetics and metabolism 117 (3), 363-368, 2016
252016
FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome
H Dai, VW Zhang, AW El‐Hattab, C Ficicioglu, M Shinawi, M Lines, ...
Clinical genetics 91 (4), 634-639, 2017
222017
Reply to Lutz-Bonengel et al.: Biparental mtDNA transmission is unlikely to be the result of nuclear mitochondrial DNA segments
S Luo, CA Valencia, J Zhang, NC Lee, J Slone, B Gui, X Wang, Z Li, ...
Proceedings of the National Academy of Sciences 116 (6), 1823-1824, 2019
172019
Noncarrier naked antigen-specific DNA vaccine generates potent antigen-specific immunologic responses and antitumor effects
CA Chen, MC Chang, WZ Sun, YL Chen, YC Chiang, CY Hsieh, SM Chen, ...
Gene therapy 16 (6), 776-787, 2009
172009
Two de novo novel mutations in one SHANK3 allele in a patient with autism and moderate intellectual disability
WB W Zhu, J Li, SM Chen, J Zhang, F Vetrini, A Braxton, C M. Eng, Y Yang, F ...
American Journal of Medical Genetics 176 (4), 973-979, 2017
12*2017
Next generation sequencing of patients with Mut methylmalonic aciduria: validation of somatic cell studies and identification of 16 novel mutations
J Chu, M Pupavac, D Watkins, X Tian, Y Feng, S Chen, R Fenter, ...
Molecular genetics and metabolism 118 (4), 264-271, 2016
122016
Advantages of highly sensitive NGS based test to detect low levels of mtDNA mutations and large deletions
H Yu, J Wang, E Schmitt, M Palculict, M Miller, S Chen, H Wang, X Tian, ...
Mitochondrion, S44-S45, 2015
12015
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