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American Journal of Medical Genetics. Part A
|
March 22, 2024
RNA analysis and computer-aided facial phenotyping help to classify a novel TRIO splice site variant
Sarina Schwartzmann, Max Zhao, Henrike Lisa Sczakiel, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology
|
June 11, 2020
Hematologist-Level Classification of Mature B-Cell Neoplasm Using Deep Learning on Multiparameter Flow Cytometry Data
Max Zhao, Nanditha Mallesh, Alexander Höllein, et al.
Journal of Inherited Metabolic Disease
|
April 7, 2018
Advances in computer-assisted syndrome recognition by the example of inborn errors of metabolism
Jean T Pantel, Max Zhao, Martin A Mensah, et al.
Patterns (New York, N.Y.)
|
October 25, 2021
Knowledge transfer to enhance the performance of deep learning models for automated classification of B cell neoplasms
Nanditha Mallesh, Max Zhao, Lisa Meintker, et al.
European Journal of Human Genetics : EJHG
|
May 15, 2023
Broadening the phenotypic and molecular spectrum of FINCA syndrome: Biallelic NHLRC2 variants in 15 novel individuals
Henrike L Sczakiel, Max Zhao, Brigitte Wollert-Wulf, et al.
Genome Medicine
|
January 10, 2018
Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis
Alexej Knaus, Jean Tori Pantel, Manuela Pendziwiat, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 6, 2019
PEDIA: prioritization of exome data by image analysis
Tzung-Chien Hsieh, Martin A Mensah, Jean T Pantel, et al.
Research Square
|
June 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 28, 2023
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
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Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
American Journal of Medical Genetics. Part A
|
March 22, 2024
RNA analysis and computer-aided facial phenotyping help to classify a novel TRIO splice site variant
Sarina Schwartzmann, Max Zhao, Henrike Lisa Sczakiel, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology
|
June 11, 2020
Hematologist-Level Classification of Mature B-Cell Neoplasm Using Deep Learning on Multiparameter Flow Cytometry Data
Max Zhao, Nanditha Mallesh, Alexander Höllein, et al.
Journal of Inherited Metabolic Disease
|
April 7, 2018
Advances in computer-assisted syndrome recognition by the example of inborn errors of metabolism
Jean T Pantel, Max Zhao, Martin A Mensah, et al.
Patterns (New York, N.Y.)
|
October 25, 2021
Knowledge transfer to enhance the performance of deep learning models for automated classification of B cell neoplasms
Nanditha Mallesh, Max Zhao, Lisa Meintker, et al.
European Journal of Human Genetics : EJHG
|
May 15, 2023
Broadening the phenotypic and molecular spectrum of FINCA syndrome: Biallelic NHLRC2 variants in 15 novel individuals
Henrike L Sczakiel, Max Zhao, Brigitte Wollert-Wulf, et al.
Genome Medicine
|
January 10, 2018
Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis
Alexej Knaus, Jean Tori Pantel, Manuela Pendziwiat, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 6, 2019
PEDIA: prioritization of exome data by image analysis
Tzung-Chien Hsieh, Martin A Mensah, Jean T Pantel, et al.
Research Square
|
June 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 28, 2023
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Page
of 1