| Noonan syndrome in diverse populations P Kruszka, AR Porras, YA Addissie, A Moresco, S Medrano, GTK Mok, ... American Journal of Medical Genetics Part A 173 (9), 2323-2334, 2017 | 89 | 2017 |
| Williams–Beuren syndrome in diverse populations P Kruszka, AR Porras, DH De Souza, A Moresco, V Huckstadt, AD Gill, ... American Journal of Medical Genetics Part A 176 (5), 1128-1136, 2018 | 75 | 2018 |
| Cornelia de Lange syndrome in diverse populations L Dowsett, AR Porras, P Kruszka, B Davis, T Hu, E Honey, E Badoe, ... American Journal of Medical Genetics Part A 179 (2), 150-158, 2019 | 50 | 2019 |
| Initiation of a medical genetics service in sub-Saharan Africa: experience of prenatal diagnosis in Cameroon A Wonkam, CN Tekendo, DJ Sama, H Zambo, S Dahoun, F Bena, ... European journal of medical genetics 54 (4), e399-e404, 2011 | 41 | 2011 |
| Holoprosencephaly Overview C Tekendo-Ngongang, M Muenke, P Kruszka In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]., 2020 | 39 | 2020 |
| Turner syndrome in diverse populations P Kruszka, YA Addissie, C Tekendo‐Ngongang, KL Jones, SK Savage, ... American Journal of Medical Genetics Part A 182 (2), 303-313, 2020 | 24 | 2020 |
| Rubinstein–Taybi syndrome in diverse populations C Tekendo‐Ngongang, B Owosela, N Fleischer, YA Addissie, B Malonga, ... American Journal of Medical Genetics Part A 182 (12), 2939-2950, 2020 | 23 | 2020 |
| Diversity and dysmorphology P Kruszka, C Tekendo-Ngongang, M Muenke Current opinion in pediatrics 31 (6), 702-707, 2019 | 23 | 2019 |
| Challenges in clinical diagnosis of Williams-Beuren syndrome in sub-Saharan Africans: case reports from Cameroon C Tekendo-Ngongang, S Dahoun, S Nguefack, S Gimelli, F Sloan-Béna, ... Molecular syndromology 5 (6), 287-292, 2014 | 21 | 2014 |
| Exome Sequencing and Congenital Heart Disease in Sub-Saharan Africa EN Ekure, A Adeyemo, H Liu, O Sokunbi, N Kalu, AF Martinez, B Owosela, ... Circulation: Genomic and Precision Medicine, doi: 10.1161/CIRCGEN.120.003108, 2021 | 19 | 2021 |
| Noonan syndrome in South Africa: clinical and molecular profiles C Tekendo-Ngongang, G Agenbag, CD Bope, AI Esterhuizen, A Wonkam Frontiers in genetics 10, 333, 2019 | 19 | 2019 |
| Novel heterozygous variants in KMT2D associated with holoprosencephaly C Tekendo‐Ngongang, P Kruszka, AF Martinez, M Muenke Clinical genetics 96 (3), 266-270, 2019 | 17 | 2019 |
| Neural Networks for Classification and Image Generation of Aging in Genetic Syndromes D Duong, P Hu, C Tekendo-Ngongang, SEL Hanchard, S Liu, ... Frontiers in Genetics 13, 864092, 2022 | 15 | 2022 |
| Neural network classifiers for images of genetic conditions with cutaneous manifestations D Duong, RL Waikel, P Hu, C Tekendo-Ngongang, BD Solomon Human Genetics and Genomics Advances 3 (1), 2022 | 14 | 2022 |
| Scoping review and classification of deep learning in medical genetics SEL Hanchard, MC Dwyer, S Liu, P Hu, C Tekendo-Ngongang, RL Waikel, ... Genetics in Medicine 24 (8), 1593-1603, 2022 | 13 | 2022 |
| Initiation of prenatal genetic diagnosis of sickle cell anaemia in Cameroon (sub‐Saharan Africa) A Wonkam, C Ngongang Tekendo, H Zambo, MA Morris Prenatal diagnosis 31 (12), 1210, 2011 | 12 | 2011 |
| The 22q11. 2 deletion syndrome in congenital heart defects: prevalence of microdeletion syndrome in Cameroon A Wonkam, R Toko, D Chelo, C Tekendo-Ngongang, S Kingue, S Dahoun Global heart 12 (2), 115-120, 2017 | 11 | 2017 |
| Beyond Trinucleotide Repeat Expansion in Fragile X Syndrome: Rare Coding and Noncoding Variants in FMR1 and Associated Phenotypes C Tekendo-Ngongang, A Grochowsky, BD Solomon, ST Yano Genes 12 (11), 1669, 2021 | 10 | 2021 |
| Perspectives on the future of dysmorphology BD Solomon, MP Adam, CT Fong, KM Girisha, JG Hall, ACE Hurst, ... American Journal of Medical Genetics Part A 191 (3), 659-671, 2023 | 9 | 2023 |
| Personalized antisense oligonucleotides ‘for free, for life’—the n-Lorem Foundation JG Gleeson, CF Bennett, JB Carroll, T Cole, J Douville, S Glass, ... Nature Medicine 29 (6), 1302-1303, 2023 | 7 | 2023 |
Prof Ambroise Wonkam, MD, DMedSc,...Division of Human Genetics - Faculty of Health Sciences - University of Cape Town - South AfricaVerified email at uct.ac.za
