Ahmad N Abou Tayoun (Ahmad Abou Tayoun, Ahmad Abou Tayoun)

ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 38

Top Venues

Genome medicine

Viruses

Genetics in medicine : official journal of the American College of Medical Genetics

Human mutation

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

Publications

Rania Najm, Lemis Yavuz, Ruchi Jain, Maha El Naofal, Sathishkumar Ramaswamy, Walid Abuhammour, Tom Loney, Norbert Nowotny, Alawi Alsheikh-Ali, Ahmad N Abou Tayoun, Richard Kumaran Kandasamy
IFIH1 loss of function predisposes to inflammatory and SARS-CoV-2-related infectious diseases. Scandinavian journal of immunology 100 (2) (2024)
Rania Najm, Lemis Yavuz, Ruchi Jain, Maha El Naofal, Sathishkumar Ramaswamy, Walid Abuhammour, Tom Loney, Norbert Nowotny, Alawi Alsheikh-Ali, Ahmad N Abou Tayoun, Richard Kumaran Kandasamy
IFIH1 loss of function predisposes to inflammatory and SARS-CoV-2-related infectious diseases. Scandinavian journal of immunology (2024)
Elena Ambrosino, Ahmad N Abou Tayoun, Marc Abramowicz, Bin Alwi Zilfalil, Tiffany F Boughtwood, Yosr Hamdi, Tim Hubbard, Kazuto Kato, Iscia Lopes-Cendes, Partha Pratim Majumder, Deborah Mascalzoni, Rokhaya Ndiaye, Michelle Ramsay, Gabriela M Repetto, Vorasuk Shotelersuk, Sherry Taylor, John C Reeder, Anna Laura Ross
The WHO genomics program of work for equitable implementation of human genomics for global health. Nature medicine (2024)
Maha El Naofal, Sathishkumar Ramaswamy, Ali Alsarhan, Ahmed Nugud, Fatima Sarfraz, Hiba Janbaz, Alan Taylor, Ruchi Jain, Nour Halabi, Sawsan Yaslam, Roudha Alfalasi, Shruti Shenbagam, Fatma Rabea, Martin Bitzan, Lemis Yavuz, Deena Wafadari, Hamda Abulhoul, Shiva Shankar, Munira Al Maazmi, Ruba Rizk, Zeinab Alloub, Haitham Elbashir, Mohamed O E Babiker, Nidheesh Chencheri, Ammar AlBanna, Meshal Sultan, Mohamed El Bitar, Safeena Kherani, Nandu Thalange, Sattar Alshryda, Roberto Di Donato, Christos Tzivinikos, Ibrar Majid, Alexandra F Freeman, Corina Gonzalez, Arif O Khan, Hisham Hamdan, Walid Abuhammour, Mohamed AlAwadhi, Abdulla AlKhayat, Alawi Alsheikh-Ali, Ahmad N Abou Tayoun
The genomic landscape of rare disorders in the Middle East. Genome medicine 15 (1) (2023)
Ruchi Jain, Fatima Rabea, Roudha Alfalasi, Mohamed Wasfy Elabiary, Ahmad N Abou Tayoun
Paternal Uniparental Isodisomy of Chromosome 2 in a Patient with Congenital Hypothyroidism: Ruling Out Recessive Inheritance or a Kinship/Laboratory Sequencing Error. The journal of applied laboratory medicine (2023)
Maha El Naofal, Sathishkumar Ramaswamy, Ali Alsarhan, Ahmed Nugud, Fatima Sarfraz, Hiba Janbaz, Alan Taylor, Ruchi Jain, Nour Halabi, Sawsan Yaslam, Roudha Alfalasi, Shruti Shenbagam, Fatma Rabea, Martin Bitzan, Lemis Yavuz, Deena Wafadari, Hamda Abulhoul, Shiva Shankar, Munira Al Maazmi, Ruba Rizk, Zeinab Alloub, Haitham Elbashir, Mohamed O E Babiker, Nidheesh Chencheri, Ammar AlBanna, Meshal Sultan, Mohamed El Bitar, Safeena Kherani, Nandu Thalange, Sattar Alshryda, Roberto Di Donato, Christos Tzivinikos, Ibrar Majid, Alexandra F Freeman, Corina Gonzalez, Arif O Khan, Hisham Hamdan, Walid Abuhammour, Mohamed AlAwadhi, Abdulla AlKhayat, Alawi Alsheikh-Ali, Ahmad N Abou Tayoun
The genomic landscape of rare disorders in the Middle East. Genome medicine 15 (1) (2023)
Maha El Naofal, Sathishkumar Ramaswamy, Ali Alsarhan, Ahmed Nugud, Fatima Sarfraz, Hiba Janbaz, Alan Taylor, Ruchi Jain, Nour Halabi, Sawsan Yaslam, Roudha Alfalasi, Shruti Shenbagam, Fatma Rabea, Martin Bitzan, Lemis Yavuz, Deena Wafadari, Hamda Abulhoul, Shiva Shankar, Munira Al Maazmi, Ruba Rizk, Zeinab Alloub, Haitham Elbashir, Mohamed O E Babiker, Nidheesh Chencheri, Ammar AlBanna, Meshal Sultan, Mohamed El Bitar, Safeena Kherani, Nandu Thalange, Sattar Alshryda, Roberto Di Donato, Christos Tzivinikos, Ibrar Majid, Alexandra F Freeman, Corina Gonzalez, Arif O Khan, Hisham Hamdan, Walid Abuhammour, Mohamed AlAwadhi, Abdulla AlKhayat, Alawi Alsheikh-Ali, Ahmad N Abou Tayoun
The genomic landscape of rare disorders in the Middle East. Genome medicine 15 (1) (2023)
Ahmad N Abou Tayoun
Unequal global implementation of genomic newborn screening. Nature reviews. Genetics (2023)
Maha El Naofal, Sathishkumar Ramaswamy, Ali Alsarhan, Ahmed Nugud, Fatima Sarfraz, Hiba Janbaz, Alan Taylor, Ruchi Jain, Nour Halabi, Sawsan Yaslam, Roudha Alfalasi, Shruti Shenbagam, Fatma Rabea, Martin Bitzan, Lemis Yavuz, Deena Wafadari, Hamda Abulhoul, Shiva Shankar, Munira Al Maazmi, Ruba Rizk, Zeinab Alloub, Haitham Elbashir, Mohamed O E Babiker, Nidheesh Chencheri, Ammar AlBanna, Meshal Sultan, Mohamed El Bitar, Safeena Kherani, Nandu Thalange, Sattar Alshryda, Roberto Di Donato, Christos Tzivinikos, Ibrar Majid, Alexandra F Freeman, Corina Gonzalez, Arif O Khan, Hisham Hamdan, Walid Abuhammour, Mohamed AlAwadhi, Abdulla AlKhayat, Alawi Alsheikh-Ali, Ahmad N Abou Tayoun
The genomic landscape of rare disorders in the Middle East. Genome medicine 15 (1) (2023)
Maha El Naofal, Sathishkumar Ramaswamy, Ali Alsarhan, Ahmed Nugud, Fatima Sarfraz, Hiba Janbaz, Alan Taylor, Ruchi Jain, Nour Halabi, Sawsan Yaslam, Roudha Alfalasi, Shruti Shenbagam, Fatma Rabea, Martin Bitzan, Lemis Yavuz, Deena Wafadari, Hamda Abulhoul, Shiva Shankar, Munira Al Maazmi, Ruba Rizk, Zeinab Alloub, Haitham Elbashir, Mohamed O E Babiker, Nidheesh Chencheri, Ammar AlBanna, Meshal Sultan, Mohamed El Bitar, Safeena Kherani, Nandu Thalange, Sattar Alshryda, Roberto Di Donato, Christos Tzivinikos, Ibrar Majid, Alexandra F Freeman, Corina Gonzalez, Arif O Khan, Hisham Hamdan, Walid Abuhammour, Mohamed AlAwadhi, Abdulla AlKhayat, Alawi Alsheikh-Ali, Ahmad N Abou Tayoun
The genomic landscape of rare disorders in the Middle East. Genome medicine 15 (1) (2023)
Maha El Naofal, Sathishkumar Ramaswamy, Ali Alsarhan, Ahmed Nugud, Fatima Sarfraz, Hiba Janbaz, Alan Taylor, Ruchi Jain, Nour Halabi, Sawsan Yaslam, Roudha Alfalasi, Shruti Shenbagam, Fatma Rabea, Martin Bitzan, Lemis Yavuz, Deena Wafadari, Hamda Abulhoul, Shiva Shankar, Munira Al Maazmi, Ruba Rizk, Zeinab Alloub, Haitham Elbashir, Mohamed O E Babiker, Nidheesh Chencheri, Ammar AlBanna, Meshal Sultan, Mohamed El Bitar, Safeena Kherani, Nandu Thalange, Sattar Alshryda, Roberto Di Donato, Christos Tzivinikos, Ibrar Majid, Alexandra F Freeman, Corina Gonzalez, Arif O Khan, Hisham Hamdan, Walid Abuhammour, Mohamed AlAwadhi, Abdulla AlKhayat, Alawi Alsheikh-Ali, Ahmad N Abou Tayoun
The genomic landscape of rare disorders in the Middle East. Genome medicine 15 (1) (2023)
Pia Weidinger, Jolanta Kolodziejek, Tom Loney, Dafalla O Kannan, Babiker Mohammed Osman, Tamer Khafaga, Brigitte Howarth, Moayyed Sher Shah, Hessa Mazrooei, Nadine Wolf, Noushad Karuvantevida, Ahmad N Abou Tayoun, Alawi Alsheikh-Ali, Jeremy V Camp, Norbert Nowotny
MERS-CoV Found in Hyalomma dromedarii Ticks Attached to Dromedary Camels at a Livestock Market, United Arab Emirates, 2019. Viruses 15 (6) (2023)
Pia Weidinger, Jolanta Kolodziejek, Tamer Khafaga, Tom Loney, Brigitte Howarth, Moayyed Sher Shah, Ahmad N Abou Tayoun, Alawi Alsheikh-Ali, Jeremy V Camp, Norbert Nowotny
Potentially Zoonotic Viruses in Wild Rodents, United Arab Emirates, 2019-A Pilot Study. Viruses 15 (3) (2023)
Pia Weidinger, Jolanta Kolodziejek, Tom Loney, Dafalla O Kannan, Babiker Mohammed Osman, Tamer Khafaga, Brigitte Howarth, Moayyed Sher Shah, Hessa Mazrooei, Nadine Wolf, Noushad Karuvantevida, Ahmad N Abou Tayoun, Alawi Alsheikh-Ali, Jeremy V Camp, Norbert Nowotny
MERS-CoV Found in Hyalomma dromedarii Ticks Attached to Dromedary Camels at a Livestock Market, United Arab Emirates, 2019. Viruses 15 (6) (2023)
Ahmad N Abou Tayoun, Alawi Alsheikh-Ali
A rapid whole-genome sequencing service for infants with rare diseases in the United Arab Emirates. Nature medicine (2023)
Pia Weidinger, Jolanta Kolodziejek, Tamer Khafaga, Tom Loney, Brigitte Howarth, Moayyed Sher Shah, Ahmad N Abou Tayoun, Alawi Alsheikh-Ali, Jeremy V Camp, Norbert Nowotny
Potentially Zoonotic Viruses in Wild Rodents, United Arab Emirates, 2019-A Pilot Study. Viruses 15 (3) (2023)
Pia Weidinger, Jolanta Kolodziejek, Tamer Khafaga, Tom Loney, Brigitte Howarth, Moayyed Sher Shah, Ahmad N Abou Tayoun, Alawi Alsheikh-Ali, Jeremy V Camp, Norbert Nowotny
Potentially Zoonotic Viruses in Wild Rodents, United Arab Emirates, 2019-A Pilot Study. Viruses 15 (3) (2023)
Pia Weidinger, Jolanta Kolodziejek, Tom Loney, Dafalla O Kannan, Babiker Mohammed Osman, Tamer Khafaga, Brigitte Howarth, Moayyed Sher Shah, Hessa Mazrooei, Nadine Wolf, Noushad Karuvantevida, Ahmad N Abou Tayoun, Alawi Alsheikh-Ali, Jeremy V Camp, Norbert Nowotny
MERS-CoV Found in Hyalomma dromedarii Ticks Attached to Dromedary Camels at a Livestock Market, United Arab Emirates, 2019. Viruses 15 (6) (2023)
Nour Halabi, Sathishkumar Ramaswamy, Maha El Naofal, Alan Taylor, Sawsan Yaslam, Ruchi Jain, Roudha Alfalasi, Shruti Shenbagam, Martin Bitzan, Lemis Yavuz, Hamda Abulhoul, Shiva Shankar, Dalwinder Janjua, Devendrasing Jadhav, Munira Mahmoud Al Maazmi, Walid Abuhammour, Alawi Alsheikh-Ali, Mohamed Al Awadhi, Abdulla Al Khayat, Ahmad N Abou Tayoun
Rapid whole genome sequencing of critically ill pediatric patients from genetically underrepresented populations. Genome medicine 14 (1) (2022)
Jiale Xiang, Xiangzhong Sun, Nana Song, Sathishkumar Ramaswamy, Ahmad N Abou Tayoun, Zhiyu Peng
Comprehensive interpretation of single-nucleotide substitutions in GJB2 reveals the genetic and phenotypic landscape of GJB2-related hearing loss. Human genetics (2022)
Sathishkumar Ramaswamy, Ruchi Jain, Maha El Naofal, Nour Halabi, Sawsan Yaslam, Alan Taylor, Ahmad N Abou Tayoun
Middle Eastern Genetic Variation Improves Clinical Annotation of the Human Genome. Journal of personalized medicine 12 (3) (2022)
Stefan Rentas, Ahmad N Abou Tayoun
Utility of droplet digital PCR and NGS-based CNV clinical assays in hearing loss diagnostics: current status and future prospects. Expert review of molecular diagnostics 21 (2) (2021)
Pia Weidinger, Jolanta Kolodziejek, Jeremy V Camp, Tom Loney, Dafalla O Kannan, Sathishkumar Ramaswamy, Ahmad N Abou Tayoun, Victor Max Corman, Norbert Nowotny
MERS-CoV in sheep, goats, and cattle, United Arab Emirates, 2019: Virological and serological investigations reveal an accidental spillover from dromedaries. Transboundary and emerging diseases (2021)
Alan Taylor, Zeinab Alloub, Ahmad N Abou Tayoun
A Simple Practical Guide to Genomic Diagnostics in a Pediatric Setting. Genes 12 (6) (2021)
Ahmad N Abou Tayoun, Khalid A Fakhro, Alawi Alsheikh-Ali, Fowzan S Alkuraya
Genomic medicine in the Middle East. Genome medicine 13 (1) (2021)
Basil M Fathalla, Ali Alsarhan, Samina Afzal, Maha El Naofal, Ahmad N Abou Tayoun
The genomic landscape of pediatric rheumatology disorders in the Middle East. Human mutation 42 (4) (2021)
Jiguang Peng, Jiale Xiang, Xiangqian Jin, Junhua Meng, Nana Song, Lisha Chen, Ahmad N Abou Tayoun, Zhiyu Peng
VIP-HL: Semi-automated ACMG/AMP variant interpretation platform for genetic hearing loss. Human mutation 42 (12) (2021)
Mayher J Patel, Marina T DiStefano, Andrea M Oza, Madeline Y Hughes, Emma H Wilcox, Sarah E Hemphill, Brandon J Cushman, Andrew R Grant, Rebecca K Siegert, Jun Shen, Alex Chapin, Nicole J Boczek, Lisa A Schimmenti, Kiyomitsu Nara, Margaret Kenna, Hela Azaiez, Kevin T Booth, Karen B Avraham, Hannie Kremer, Andrew J Griffith, Heidi L Rehm, Sami S Amr, Ahmad N Abou Tayoun, null null
Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss. Genetics in medicine : official journal of the American College of Medical Genetics 23 (11) (2021)
Tom Loney, Hamda Khansaheb, Sathishkumar Ramaswamy, Divinlal Harilal, Zulfa Omar Deesi, Rupa Murthy Varghese, Aydah Belal Al Ali, Anees Khadeeja, Hanan Al Suwaidi, Abdulmajeed Alkhajeh, Laila Mohamed AlDabal, Mohammed Uddin, Mubarak Al Faresi, Madhvi Joshi, Abiola Senok, Norbert Nowotny, Alawi Alsheikh-Ali, Ahmad N Abou Tayoun
Genotype-phenotype correlation identified a novel SARS-CoV-2 variant possibly linked to severe disease. Transboundary and emerging diseases (2021)
Stefan Rentas, Komal S Rathi, Maninder Kaur, Pichai Raman, Ian D Krantz, Mahdi Sarmady, Ahmad N Abou Tayoun
Diagnosing Cornelia de Lange syndrome and related neurodevelopmental disorders using RNA sequencing. Genetics in medicine : official journal of the American College of Medical Genetics 22 (5) (2020)
Andrea M Oza, Marina T DiStefano, Sarah E Hemphill, Brandon J Cushman, Andrew R Grant, Rebecca K Siegert, Jun Shen, Alex Chapin, Nicole J Boczek, Lisa A Schimmenti, Jaclyn B Murry, Linda Hasadsri, Kiyomitsu Nara, Margaret Kenna, Kevin T Booth, Hela Azaiez, Andrew Griffith, Karen B Avraham, Hannie Kremer, Michael J Bamshad, Sami S Amr, Ahmad N Abou Tayoun, null null
Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss. Human mutation 39 (11) (2019)
Ahmad N Abou Tayoun, Heather Mason-Suares
Considerations for whole exome sequencing unique to prenatal care. Human genetics 139 (9) (2019)
Perry Evans, Chao Wu, Amanda Lindy, Dianalee A McKnight, Matthew Lebo, Mahdi Sarmady, Ahmad N Abou Tayoun
Genetic variant pathogenicity prediction trained using disease-specific clinical sequencing data sets. Genome research 29 (7) (2019)
Jun Shen, Andrea M Oza, Ignacio Del Castillo, Hatice Duzkale, Tatsuo Matsunaga, Arti Pandya, Hyunseok P Kang, Rebecca Mar-Heyming, Saurav Guha, Krista Moyer, Christine Lo, Margaret Kenna, John J Alexander, Yan Zhang, Yoel Hirsch, Minjie Luo, Ye Cao, Kwong-Wai Choy, Yen-Fu Cheng, Karen B Avraham, Xinhua Hu, Gema Garrido, Miguel Angel Moreno-Pelayo, John Greinwald, Kejian Zhang, Yukun Zeng, Zippora Brownstein, Lina Basel-Salmon, Bella Davidov, Moshe Frydman, Tzvi Weiden, Narasimhan Nagan, Alecia Willis, Sarah E Hemphill, Andrew R Grant, Rebecca K Siegert, Marina T DiStefano, Sami S Amr, Michael J Bamshad, Ahmad N Abou Tayoun, null null
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel. Genetics in medicine : official journal of the American College of Medical Genetics 21 (11) (2019)
Ahmad N Abou Tayoun, Tina Pesaran, Marina T DiStefano, Andrea M Oza, Michael J Bamshad, Leslie G Biesecker, Steven M Harrison, null null
Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion. Human mutation 39 (11) (2018)
Ahmad N Abou Tayoun, Nancy B Spinner, Heidi L Rehm, Robert C Green, Diana W Bianchi
Prenatal DNA Sequencing: Clinical, Counseling, and Diagnostic Laboratory Considerations. Prenatal diagnosis 38 (1) (2017)
Sami S Amr, Saeed H Al Turki, Matthew S Lebo, Mahdi Sarmady, Michael J Bamshad, Ahmad N Abou Tayoun
Using large sequencing data sets to refine intragenic disease regions and prioritize clinical variant interpretation. Genetics in medicine : official journal of the American College of Medical Genetics 19 (5) (2016)
Ahmad N Abou Tayoun, Saeed H Al Turki, Andrea M Oza, Mark J Bowser, Amy L Hernandez, Birgit H Funke, Michael J Bamshad, Sami S Amr
Improving hearing loss gene testing: a systematic review of gene evidence toward more efficient next-generation sequencing-based diagnostic testing and interpretation. Genetics in medicine : official journal of the American College of Medical Genetics 18 (6) (2015)

Ahmad N Abou Tayoun.css-eqlu8i{font-size:small;padding-left:4px;} (Ahmad Abou Tayoun, Ahmad Abou Tayoun)

Publication Activity (10 Years)

Top Topics

Top Venues

Ahmad N Abou Tayoun (Ahmad Abou Tayoun, Ahmad Abou Tayoun)