C. Tekendo-Ngongang

发表

Noonan syndrome on the African Continent

P. Kruszka, C. Tekendo-Ngongang, 2020, Birth defects research.

Noonan Syndrome in South Africa: Clinical and Molecular Profiles

A. Wonkam, C. Tekendo-Ngongang, G. Agenbag, 2019, Front. Genet..

Cornelia de Lange syndrome in diverse populations

A. R. Porras, I. Krantz, E. Roeder, 2019, American journal of medical genetics. Part A.

Challenges in Clinical Diagnosis of Williams-Beuren Syndrome in Sub-Saharan Africans: Case Reports from Cameroon

S. Gimelli, A. Wonkam, C. Tekendo-Ngongang, 2014, Molecular Syndromology.

Noonan syndrome in diverse populations

A. R. Porras, Yonit A. Addissie, R. Stevenson, 2017, American journal of medical genetics. Part A.

Williams–Beuren syndrome in diverse populations

A. R. Porras, Yonit A. Addissie, A. Adeyemo, 2018, American journal of medical genetics. Part A.

Comorbidity of congenital heart defects and holoprosencephaly is likely genetically driven and gene‐specific

P. Kruszka, M. Muenke, C. Tekendo-Ngongang, 2020, American journal of medical genetics. Part C, Seminars in medical genetics.

The 22q11.2 Deletion Syndrome in Congenital Heart Defects: Prevalence of Microdeletion Syndrome in Cameroon.

A. Wonkam, C. Tekendo-Ngongang, S. Kingue, 2017, Global heart.

Scoping review and classification of deep learning in medical genetics.

B. Solomon, P. Hu, C. Tekendo-Ngongang, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

MECP2 duplication syndrome in a patient from Cameroon

S. Gimelli, M. Morris, A. Wonkam, 2020, American journal of medical genetics. Part A.

Perspectives on the future of dysmorphology

P. Krawitz, B. Solomon, S. Phadke, 2022, American journal of medical genetics. Part A.

Diversity and dysmorphology.

P. Kruszka, M. Muenke, C. Tekendo-Ngongang, 2019, Current opinion in pediatrics.

Neural network classifiers for images of genetic conditions with cutaneous manifestations

Dat Van Duong, Ping Hu, Dat Duong, 2021, HGG advances.

Proof-of-principle neural network models for classification, attribution, creation, style-mixing, and morphing of image data for genetic conditions

P. Hu, C. Tekendo-Ngongang, R. Waikel, 2021, medRxiv.

Turner syndrome in diverse populations

Yonit A. Addissie, A. Mégarbané, V. Dissanayake, 2019, American journal of medical genetics. Part A.

Exome Sequencing and Congenital Heart Disease in Sub-Saharan Africa.

Yonit A. Addissie, A. Adeyemo, P. Kruszka, 2021, Circulation. Genomic and precision medicine.

Beyond Trinucleotide Repeat Expansion in Fragile X Syndrome: Rare Coding and Noncoding Variants in FMR1 and Associated Phenotypes

B. Solomon, C. Tekendo-Ngongang, Angela Grochowsky, 2021, Genes.

Cross‐cultural representations of conjoined twins

Marc S. Williams, C. Tekendo-Ngongang, K. Williams, 2021, American journal of medical genetics. Part C, Seminars in medical genetics.

Neural Networks for Classification and Image Generation of Aging in Genetic Syndromes

B. Solomon, P. Hu, C. Tekendo-Ngongang, 2021, Frontiers in Genetics.

Novel heterozygous variants in KMT2D associated with holoprosencephaly

P. Kruszka, M. Muenke, C. Tekendo-Ngongang, 2019, Clinical genetics.

Rubinstein–Taybi syndrome in diverse populations

Yonit A. Addissie, R. Stevenson, N. Brunetti‐Pierri, 2020, American journal of medical genetics. Part A.

New Mitochondrial Disease Identified In Monozygotic Twin Boys

V. Jobanputra, R. Happle, B. Gelb, 2023, American journal of medical genetics. Part A.

Bridging the language gap - A call for the wider use of Human phenotype ontology by non-geneticist clinicians when requesting genomic tests.

R. Pengelly, J. Self, C. Tekendo-Ngongang, 2022, European journal of medical genetics.

A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family

S. Leal, K. Esoh, A. Wonkam, 2021, Genes.

Personalized antisense oligonucleotides ‘for free, for life’ — the n-Lorem Foundation

J. Gleeson, C. Bennett, Tracy A. Cole, 2023, Nature Network Boston.

Generative Artificial Intelligence Methods for Pediatric Genetics Education

Dat Van Duong, P. Hu, C. Tekendo-Ngongang, 2023, medRxiv.