Cedrik Tekendo-Ngongang

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 11

Top Topics

Convolutional Neural Network

Botulinum Toxin

Top Venues

Nature medicine

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Dat Duong, Anna Rose Johny, Suzanna Ledgister Hanchard, Christopher Fortney, Kendall Flaharty, Fabio Hellmann, Ping Hu, Behnam Javanmardi, Shahida Moosa, Tanviben Patel, Susan Persky, Ömer Sümer, Cedrik Tekendo-Ngongang, Hellen Lesmann, Tzung-Chien Hsieh, Rebekah L Waikel, Elisabeth André, Peter Krawitz, Benjamin D Solomon
Comparison of clinical geneticist and computer visual attention in assessing genetic conditions. PLoS genetics 20 (2) (2024)
Dat Duong, Anna Rose Johny, Suzanna Ledgister Hanchard, Christopher Fortney, Kendall Flaharty, Fabio Hellmann, Ping Hu, Behnam Javanmardi, Shahida Moosa, Tanviben Patel, Susan Persky, Ömer Sümer, Cedrik Tekendo-Ngongang, Hellen Lesmann, Tzung-Chien Hsieh, Rebekah L Waikel, Elisabeth André, Peter Krawitz, Benjamin D Solomon
Comparison of clinical geneticist and computer visual attention in assessing genetic conditions. PLoS genetics 20 (2) (2024)
Dat Duong, Anna Rose Johny, Suzanna Ledgister Hanchard, Christopher Fortney, Kendall Flaharty, Fabio Hellmann, Ping Hu, Behnam Javanmardi, Shahida Moosa, Tanviben Patel, Susan Persky, Ömer Sümer, Cedrik Tekendo-Ngongang, Hellen Lesmann, Tzung-Chien Hsieh, Rebekah L Waikel, Elisabeth André, Peter Krawitz, Benjamin D Solomon
Comparison of clinical geneticist and computer visual attention in assessing genetic conditions. PLoS genetics 20 (2) (2024)
Dat Duong, Anna Rose Johny, Suzanna Ledgister Hanchard, Christopher Fortney, Kendall Flaharty, Fabio Hellmann, Ping Hu, Behnam Javanmardi, Shahida Moosa, Tanviben Patel, Susan Persky, Ömer Sümer, Cedrik Tekendo-Ngongang, Hellen Lesmann, Tzung-Chien Hsieh, Rebekah L Waikel, Elisabeth André, Peter Krawitz, Benjamin D Solomon
Comparison of clinical geneticist and computer visual attention in assessing genetic conditions. PLoS genetics 20 (2) (2024)
Dat Duong, Anna Rose Johny, Suzanna Ledgister Hanchard, Christopher Fortney, Kendall Flaharty, Fabio Hellmann, Ping Hu, Behnam Javanmardi, Shahida Moosa, Tanviben Patel, Susan Persky, Ömer Sümer, Cedrik Tekendo-Ngongang, Hellen Lesmann, Tzung-Chien Hsieh, Rebekah L Waikel, Elisabeth André, Peter Krawitz, Benjamin D Solomon
Comparison of clinical geneticist and computer visual attention in assessing genetic conditions. PLoS genetics 20 (2) (2024)
Dat Duong, Anna Rose Johny, Suzanna Ledgister Hanchard, Christopher Fortney, Kendall Flaharty, Fabio Hellmann, Ping Hu, Behnam Javanmardi, Shahida Moosa, Tanviben Patel, Susan Persky, Ömer Sümer, Cedrik Tekendo-Ngongang, Hellen Lesmann, Tzung-Chien Hsieh, Rebekah L Waikel, Elisabeth André, Peter Krawitz, Benjamin D Solomon
Comparison of clinical geneticist and computer visual attention in assessing genetic conditions. PLoS genetics 20 (2) (2024)
Joseph G Gleeson, C Frank Bennett, Jeffrey B Carroll, Tracy Cole, Julie Douville, Sarah Glass, Cedrik Tekendo-Ngongang, Amy C Williford, Stanley T Crooke
Personalized antisense oligonucleotides 'for free, for life' - the n-Lorem Foundation. Nature medicine (2023)
Cedrik Tekendo-Ngongang, Angela Grochowsky, Benjamin D Solomon, Sho T Yano
Beyond Trinucleotide Repeat Expansion in Fragile X Syndrome: Rare Coding and Noncoding Variants in FMR1 and Associated Phenotypes. Genes 12 (11) (2021)
Noluthando Manyisa, Isabelle Schrauwen, Leonardo Alves de Souza Rios, Shaheen Mowla, Cedrik Tekendo-Ngongang, Kalinka Popel, Kevin Kum Esoh, Thashi Bharadwaj, Liz M Nouel Saied, Anushree Acharya, Abdul Nasir, Edmond Wonkam-Tingang, Carmen de Kock, Collet Dandara, Suzanne M Leal, Ambroise Wonkam
A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family. Genes 12 (11) (2021)
Cedrik Tekendo-Ngongang, Sophie Dahoun, Séraphin Nguefack, Isabelle Moix, Stefania Gimelli, Huguette Zambo, Michael A Morris, Frédérique Sloan-Béna, Ambroise Wonkam
MECP2 duplication syndrome in a patient from Cameroon. American journal of medical genetics. Part A 182 (4) (2020)
Cedrik Tekendo-Ngongang, Babajide Owosela, Maximilian Muenke, Paul S Kruszka
Comorbidity of congenital heart defects and holoprosencephaly is likely genetically driven and gene-specific. American journal of medical genetics. Part C, Seminars in medical genetics 184 (1) (2020)