Amjad Khan

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 16

Top Venues

Molecular genetics & genomic medicine

Cell death & disease

Neurogenetics

Genes

King Abdullah International Medical Research Center

China Medical University (PHD)

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

Affiliation History

King Abdullah International Medical Research Center Jan 25 2019

Saudi Arabia

Postdoct :: Developmental Medicine

Education History

China Medical University Sep 01 2015 - Jun 28 2018

China

PHD :: Genomics

Publications

Elizabeth A Werren, Emily R Peirent, Henna Jantti, Alba Guxholli, Kinshuk Raj Srivastava, Naama Orenstein, Vinodh Narayanan, Wojciech Wiszniewski, Mateusz Dawidziuk, Pawel Gawlinski, Muhammad Umair, Amjad Khan, Shahid Niaz Khan, David Genevieve, Daphné Lehalle, K L I van Gassen, Jacques C Giltay, Renske Oegema, Richard H van Jaarsveld, Rafiullah Rafiullah, Gudrun A Rappold, Rachel Rabin, John G Pappas, Marsha M Wheeler, Michael J Bamshad, Yao-Chang Tsan, Matthew B Johnson, Catherine E Keegan, Anshika Srivastava, Stephanie L Bielas
Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations. Cell death & disease 15 (5) (2024)
Amjad Khan, Bushra Al Shamsi, Maryam Al Shehhi, Amna A Kashgari, Aaisha Al Balushi, Fahad A Al Dihan, Mohannad A Alghamdi, Abothnain Manal, Ana C González-Álvarez, Stefan T Arold, Wafaa Eyaid
Further delineation of Wiedemann-Rautenstrauch syndrome linked with POLR3A. Molecular genetics & genomic medicine 12 (3) (2024)
Elizabeth A Werren, Emily R Peirent, Henna Jantti, Alba Guxholli, Kinshuk Raj Srivastava, Naama Orenstein, Vinodh Narayanan, Wojciech Wiszniewski, Mateusz Dawidziuk, Pawel Gawlinski, Muhammad Umair, Amjad Khan, Shahid Niaz Khan, David Genevieve, Daphné Lehalle, K L I van Gassen, Jacques C Giltay, Renske Oegema, Richard H van Jaarsveld, Rafiullah Rafiullah, Gudrun A Rappold, Rachel Rabin, John G Pappas, Marsha M Wheeler, Michael J Bamshad, Yao-Chang Tsan, Matthew B Johnson, Catherine E Keegan, Anshika Srivastava, Stephanie L Bielas
Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations. Cell death & disease 15 (5) (2024)
Amjad Khan, Bushra Al Shamsi, Maryam Al Shehhi, Amna A Kashgari, Aaisha Al Balushi, Fahad A Al Dihan, Mohannad A Alghamdi, Abothnain Manal, Ana C González-Álvarez, Stefan T Arold, Wafaa Eyaid
Further delineation of Wiedemann-Rautenstrauch syndrome linked with POLR3A. Molecular genetics & genomic medicine 12 (3) (2024)
null Saima, Amjad Khan, Sajid Ali, Jiuhong Jiang, Zhichao Miao, Atif Kamil, Shahid Niaz Khan, Stefan T Arold
Clinical genomics expands the link between erroneous cell division, primary microcephaly and intellectual disability. Neurogenetics 25 (3) (2024)
Amjad Khan, Bushra Al Shamsi, Maryam Al Shehhi, Amna A Kashgari, Aaisha Al Balushi, Fahad A Al Dihan, Mohannad A Alghamdi, Abothnain Manal, Ana C González-Álvarez, Stefan T Arold, Wafaa Eyaid
Further delineation of Wiedemann-Rautenstrauch syndrome linked with POLR3A. Molecular genetics & genomic medicine 12 (3) (2024)
Amjad Khan, Bushra Al Shamsi, Maryam Al Shehhi, Amna A Kashgari, Aaisha Al Balushi, Fahad A Al Dihan, Mohannad A Alghamdi, Abothnain Manal, Ana C González-Álvarez, Stefan T Arold, Wafaa Eyaid
Further delineation of Wiedemann-Rautenstrauch syndrome linked with POLR3A. Molecular genetics & genomic medicine (2024)
Amjad Khan, Bushra Al Shamsi, Maryam Al Shehhi, Amna A Kashgari, Aaisha Al Balushi, Fahad A Al Dihan, Mohannad A Alghamdi, Abothnain Manal, Ana C González-Álvarez, Stefan T Arold, Wafaa Eyaid
Further delineation of Wiedemann-Rautenstrauch syndrome linked with POLR3A. Molecular genetics & genomic medicine 12 (3) (2024)
null Saima, Amjad Khan, Sajid Ali, Jiuhong Jiang, Zhichao Miao, Atif Kamil, Shahid Niaz Khan, Stefan T Arold
Clinical genomics expands the link between erroneous cell division, primary microcephaly and intellectual disability. Neurogenetics (2024)
Elizabeth A Werren, Emily R Peirent, Henna Jantti, Alba Guxholli, Kinshuk Raj Srivastava, Naama Orenstein, Vinodh Narayanan, Wojciech Wiszniewski, Mateusz Dawidziuk, Pawel Gawlinski, Muhammad Umair, Amjad Khan, Shahid Niaz Khan, David Genevieve, Daphné Lehalle, K L I van Gassen, Jacques C Giltay, Renske Oegema, Richard H van Jaarsveld, Rafiullah Rafiullah, Gudrun A Rappold, Rachel Rabin, John G Pappas, Marsha M Wheeler, Michael J Bamshad, Yao-Chang Tsan, Matthew B Johnson, Catherine E Keegan, Anshika Srivastava, Stephanie L Bielas
Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations. Cell death & disease 15 (5) (2024)
Hamed Nawaz, null Mujahid, Sher Alam Khan, Farhana Bibi, Ahmed Waqas, Abdul Bari, null Fardous, Niamatullah Khan, Nazif Muhammad, Amjad Khan, Sohail Aziz Paracha, Qamre Alam, Mohammad Azhar Kamal, Misbahuddin M Rafeeq, Noor Muhammad, Fayaz Ul Haq, Shazia Khan, Arif Mahmood, Saadullah Khan, Muhammad Umair
Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome. Genes 14 (5) (2023)
Anwar Ullah, Zhaohan Lin, Muhammad Younus, Sarfraz Shafiq, Shazia Khan, Memoona Rasheed, Arif Mahmood, Amany I Alqosaibi, Mohammed Ali Alshehri, Amjad Khan, Muhammad Umair
Homozygous missense variant in POPDC3 causes recessive limb-girdle muscular dystrophy type 26. The journal of gene medicine 24 (4) (2022)
Amjad Khan, Manal Alaamery, Salam Massadeh, Abdulrahman Obaid, Amna A Kashgari, Christopher A Walsh, Wafaa Eyaid
PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in microcephaly. Clinical genetics 98 (1) (2020)
Amjad Khan, Zhichiao Miao, Muhammad Umair, Amir Ullah, Mohammad A Alshabeeb, Muhammad Bilal, Farooq Ahmad, Gudrun A Rappold, Muhammad Ansar, Raphaël Carapito
Two Cases of Recessive Intellectual Disability Caused by NDST1 and METTL23 Variants. Genes 11 (9) (2020)
Amjad Khan, Muhammad Umair, Rania Abdulfattah Sharaf, Muhammad Ismail Khan, Amir Ullah, Safdar Abbas, Nargis Shaheen, Muhammad Bilal, Farooq Ahamd
Novel homozygous variant in the TPO gene associated with congenital hypothyroidism and mild-intellectual disability. Human genome variation 7 (1) (2020)
Amjad Khan, Shirui Han, Rongrong Wang, Muhammad Ansar, Wasim Ahmad, Xue Zhang
Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort. Molecular genetics & genomic medicine 7 (9) (2019)

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Publication Activity (10 Years)

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Amjad Khan