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Georgi Z Genchev

Showing results (11-20 of 26) with videos related to

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Orphanet Journal of Rare Diseases|June 9, 2021
Demographics, in-hospital analysis, and prevalence of 33 rare diseases with effective treatment in ShanghaiXiaoshu Cai, Georgi Z Genchev, Ping He, et al.
Frontiers in Bioengineering and Biotechnology|November 16, 2020
Nuclear Segmentation in Histopathological Images Using Two-Stage Stacked U-Nets With Attention MechanismYan Kong, Georgi Z Genchev, Xiaolei Wang, et al.
Frontiers in Genetics|September 24, 2019
Functional Site Discovery From Incomplete Training Data: A Case Study With Nucleic Acid-Binding ProteinsWenchuan Wang, Robert Langlois, Marina Langlois, et al.
Neurogenetics|June 15, 2021
Pitt-Hopkins syndrome: phenotypic and genotypic description of four unrelated patients and structural analysis of corresponding missense mutationsTingting Zhao, Georgi Z Genchev, Shengnan Wu, et al.
Biophysical Journal|July 5, 2008
Stabilization provided by neighboring strands is critical for the mechanical stability of proteinsDeepak Sharma, Gang Feng, Dingyue Khor, et al.
Journal of Medical Internet Research|June 2, 2021
Evaluation Framework for Successful Artificial Intelligence-Enabled Clinical Decision Support Systems: Mixed Methods StudyMengting Ji, Georgi Z Genchev, Hengye Huang, et al.
Orphanet Journal of Rare Diseases|February 8, 2024
Clinical and genetic characterization of 47 Chinese pediatric patients with Pitt-Hopkins syndrome: a retrospective studyTingting Zhao, Shengnan Wu, Yiping Shen, et al.
Communications Biology|September 16, 2022
FVC as an adaptive and accurate method for filtering variants from popular NGS analysis pipelinesYongyong Ren, Yan Kong, Xiaocheng Zhou, et al.
Orphanet Journal of Rare Diseases|June 15, 2023
Correction: Multivariate analysis and model building for classifying patients in the peroxisomal disorders X-linked adrenoleukodystrophy and Zellweger syndrome in Chinese pediatric patientsZhixing Zhu, Georgi Z Genchev, Yanmin Wang, et al.
Frontiers in Molecular Biosciences|August 1, 2020
Improving the Diagnosis of Phenylketonuria by Using a Machine Learning-Based Screening Model of Neonatal MRM DataZhixing Zhu, Jianlei Gu, Georgi Z Genchev, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Orphanet Journal of Rare Diseases|June 9, 2021
Demographics, in-hospital analysis, and prevalence of 33 rare diseases with effective treatment in ShanghaiXiaoshu Cai, Georgi Z Genchev, Ping He, et al.
Frontiers in Bioengineering and Biotechnology|November 16, 2020
Nuclear Segmentation in Histopathological Images Using Two-Stage Stacked U-Nets With Attention MechanismYan Kong, Georgi Z Genchev, Xiaolei Wang, et al.
Frontiers in Genetics|September 24, 2019
Functional Site Discovery From Incomplete Training Data: A Case Study With Nucleic Acid-Binding ProteinsWenchuan Wang, Robert Langlois, Marina Langlois, et al.
Neurogenetics|June 15, 2021
Pitt-Hopkins syndrome: phenotypic and genotypic description of four unrelated patients and structural analysis of corresponding missense mutationsTingting Zhao, Georgi Z Genchev, Shengnan Wu, et al.
Biophysical Journal|July 5, 2008
Stabilization provided by neighboring strands is critical for the mechanical stability of proteinsDeepak Sharma, Gang Feng, Dingyue Khor, et al.
Journal of Medical Internet Research|June 2, 2021
Evaluation Framework for Successful Artificial Intelligence-Enabled Clinical Decision Support Systems: Mixed Methods StudyMengting Ji, Georgi Z Genchev, Hengye Huang, et al.
Orphanet Journal of Rare Diseases|February 8, 2024
Clinical and genetic characterization of 47 Chinese pediatric patients with Pitt-Hopkins syndrome: a retrospective studyTingting Zhao, Shengnan Wu, Yiping Shen, et al.
Communications Biology|September 16, 2022
FVC as an adaptive and accurate method for filtering variants from popular NGS analysis pipelinesYongyong Ren, Yan Kong, Xiaocheng Zhou, et al.
Orphanet Journal of Rare Diseases|June 15, 2023
Correction: Multivariate analysis and model building for classifying patients in the peroxisomal disorders X-linked adrenoleukodystrophy and Zellweger syndrome in Chinese pediatric patientsZhixing Zhu, Georgi Z Genchev, Yanmin Wang, et al.
Frontiers in Molecular Biosciences|August 1, 2020
Improving the Diagnosis of Phenylketonuria by Using a Machine Learning-Based Screening Model of Neonatal MRM DataZhixing Zhu, Jianlei Gu, Georgi Z Genchev, et al.
Pageof 3