Khalid A Fakhro (Khalid Fakhro)

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 41

Top Venues

Nature communications

Molecular psychiatry

Genome medicine

NPJ genomic medicine

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

Publications

Waleed Aamer, Aljazi Al-Maraghi, Najeeb Syed, Geethanjali Devadoss Gandhi, Elbay Aliyev, Alya A Al-Kurbi, Omayma Al-Saei, Muhammad Kohailan, Navaneethakrishnan Krishnamoorthy, Sasirekha Palaniswamy, Khulod Al-Malki, Saleha Abbasi, Nourhen Agrebi, Fatemeh Abbaszadeh, Ammira S Al-Shabeeb Akil, Ramin Badii, Tawfeg Ben-Omran, Bernice Lo, null null, Younes Mokrab, Khalid A Fakhro
Burden of Mendelian disorders in a large Middle Eastern biobank. Genome medicine 16 (1) (2024)
Viorica Chelban, Henriette Aksnes, Reza Maroofian, Lauren C LaMonica, Luis Seabra, Anette Siggervåg, Perrine Devic, Hanan E Shamseldin, Jana Vandrovcova, David Murphy, Anne-Claire Richard, Olivier Quenez, Antoine Bonnevalle, M Natalia Zanetti, Rauan Kaiyrzhanov, Vincenzo Salpietro, Stephanie Efthymiou, Lucia V Schottlaender, Heba Morsy, Annarita Scardamaglia, Ambreen Tariq, Alistair T Pagnamenta, Ajia Pennavaria, Liv S Krogstad, Åse K Bekkelund, Alessia Caiella, Nina Glomnes, Kirsten M Brønstad, Sandrine Tury, Andrés Moreno De Luca, Anne Boland-Auge, Robert Olaso, Jean François Deleuze, Mathieu Anheim, Benjamin Cretin, Barbara Vona, Fahad S Al-Ajlan, Firdous Abdulwahab, Jean-Luc Battini, Rojan İpek, Peter Bauer, Giovanni Zifarelli, Serdal Gungor, Semra Hiz Kurul, Hanns Lochmüller, Sahar Isa Da'as, Khalid A Fakhro, Alicia Gómez-Pascual, Juan A Botía, Nicholas W Wood, Rita Horvath, Andreas M Ernst, James E Rothman, Meriel McEntagart, Yanick J Crow, Fowzan Sami Alkuraya, Gaël Nicolas, null null, Thomas Arnesen, Henry Houlden
Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications. Nature communications 15 (1) (2024)
Waleed Aamer, Aljazi Al-Maraghi, Najeeb Syed, Geethanjali Devadoss Gandhi, Elbay Aliyev, Alya A Al-Kurbi, Omayma Al-Saei, Muhammad Kohailan, Navaneethakrishnan Krishnamoorthy, Sasirekha Palaniswamy, Khulod Al-Malki, Saleha Abbasi, Nourhen Agrebi, Fatemeh Abbaszadeh, Ammira S Al-Shabeeb Akil, Ramin Badii, Tawfeg Ben-Omran, Bernice Lo, null null, Younes Mokrab, Khalid A Fakhro
Burden of Mendelian disorders in a large Middle Eastern biobank. Genome medicine 16 (1) (2024)
Waleed Aamer, Aljazi Al-Maraghi, Najeeb Syed, Geethanjali Devadoss Gandhi, Elbay Aliyev, Alya A Al-Kurbi, Omayma Al-Saei, Muhammad Kohailan, Navaneethakrishnan Krishnamoorthy, Sasirekha Palaniswamy, Khulod Al-Malki, Saleha Abbasi, Nourhen Agrebi, Fatemeh Abbaszadeh, Ammira S Al-Shabeeb Akil, Ramin Badii, Tawfeg Ben-Omran, Bernice Lo, null null, Younes Mokrab, Khalid A Fakhro
Burden of Mendelian disorders in a large Middle Eastern biobank. Genome medicine 16 (1) (2024)
Viorica Chelban, Henriette Aksnes, Reza Maroofian, Lauren C LaMonica, Luis Seabra, Anette Siggervåg, Perrine Devic, Hanan E Shamseldin, Jana Vandrovcova, David Murphy, Anne-Claire Richard, Olivier Quenez, Antoine Bonnevalle, M Natalia Zanetti, Rauan Kaiyrzhanov, Vincenzo Salpietro, Stephanie Efthymiou, Lucia V Schottlaender, Heba Morsy, Annarita Scardamaglia, Ambreen Tariq, Alistair T Pagnamenta, Ajia Pennavaria, Liv S Krogstad, Åse K Bekkelund, Alessia Caiella, Nina Glomnes, Kirsten M Brønstad, Sandrine Tury, Andrés Moreno De Luca, Anne Boland-Auge, Robert Olaso, Jean François Deleuze, Mathieu Anheim, Benjamin Cretin, Barbara Vona, Fahad S Al-Ajlan, Firdous Abdulwahab, Jean-Luc Battini, Rojan İpek, Peter Bauer, Giovanni Zifarelli, Serdal Gungor, Semra Hiz Kurul, Hanns Lochmüller, Sahar Isa Da'as, Khalid A Fakhro, Alicia Gómez-Pascual, Juan A Botía, Nicholas W Wood, Rita Horvath, Andreas M Ernst, James E Rothman, Meriel McEntagart, Yanick J Crow, Fowzan Sami Alkuraya, Gaël Nicolas, null null, Thomas Arnesen, Henry Houlden
Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications. Nature communications 15 (1) (2024)
Rulan Shaath, Aljazi Al-Maraghi, Haytham Ali, Jehan AlRayahi, Adam D Kennedy, Karen L DeBalsi, Sura Hussein, Najwa Elbashir, Sujitha S Padmajeya, Sasirekha Palaniswamy, Sarah H Elsea, Ammira A Akil, Noha A Yousri, Khalid A Fakhro
Integrating Genome Sequencing and Untargeted Metabolomics in Monozygotic Twins with a Rare Complex Neurological Disorder. Metabolites 14 (3) (2024)
Rulan Shaath, Aljazi Al-Maraghi, Haytham Ali, Jehan AlRayahi, Adam D Kennedy, Karen L DeBalsi, Sura Hussein, Najwa Elbashir, Sujitha S Padmajeya, Sasirekha Palaniswamy, Sarah H Elsea, Ammira A Akil, Noha A Yousri, Khalid A Fakhro
Integrating Genome Sequencing and Untargeted Metabolomics in Monozygotic Twins with a Rare Complex Neurological Disorder. Metabolites 14 (3) (2024)
Viorica Chelban, Henriette Aksnes, Reza Maroofian, Lauren C LaMonica, Luis Seabra, Anette Siggervåg, Perrine Devic, Hanan E Shamseldin, Jana Vandrovcova, David Murphy, Anne-Claire Richard, Olivier Quenez, Antoine Bonnevalle, M Natalia Zanetti, Rauan Kaiyrzhanov, Vincenzo Salpietro, Stephanie Efthymiou, Lucia V Schottlaender, Heba Morsy, Annarita Scardamaglia, Ambreen Tariq, Alistair T Pagnamenta, Ajia Pennavaria, Liv S Krogstad, Åse K Bekkelund, Alessia Caiella, Nina Glomnes, Kirsten M Brønstad, Sandrine Tury, Andrés Moreno De Luca, Anne Boland-Auge, Robert Olaso, Jean François Deleuze, Mathieu Anheim, Benjamin Cretin, Barbara Vona, Fahad S Al-Ajlan, Firdous Abdulwahab, Jean-Luc Battini, Rojan İpek, Peter Bauer, Giovanni Zifarelli, Serdal Gungor, Semra Hiz Kurul, Hanns Lochmüller, Sahar Isa Da'as, Khalid A Fakhro, Alicia Gómez-Pascual, Juan A Botía, Nicholas W Wood, Rita Horvath, Andreas M Ernst, James E Rothman, Meriel McEntagart, Yanick J Crow, Fowzan Sami Alkuraya, Gaël Nicolas, null null, Thomas Arnesen, Henry Houlden
Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications. Nature communications 15 (1) (2024)
Viorica Chelban, Henriette Aksnes, Reza Maroofian, Lauren C LaMonica, Luis Seabra, Anette Siggervåg, Perrine Devic, Hanan E Shamseldin, Jana Vandrovcova, David Murphy, Anne-Claire Richard, Olivier Quenez, Antoine Bonnevalle, M Natalia Zanetti, Rauan Kaiyrzhanov, Vincenzo Salpietro, Stephanie Efthymiou, Lucia V Schottlaender, Heba Morsy, Annarita Scardamaglia, Ambreen Tariq, Alistair T Pagnamenta, Ajia Pennavaria, Liv S Krogstad, Åse K Bekkelund, Alessia Caiella, Nina Glomnes, Kirsten M Brønstad, Sandrine Tury, Andrés Moreno De Luca, Anne Boland-Auge, Robert Olaso, Jean François Deleuze, Mathieu Anheim, Benjamin Cretin, Barbara Vona, Fahad S Al-Ajlan, Firdous Abdulwahab, Jean-Luc Battini, Rojan İpek, Peter Bauer, Giovanni Zifarelli, Serdal Gungor, Semra Hiz Kurul, Hanns Lochmüller, Sahar Isa Da'as, Khalid A Fakhro, Alicia Gómez-Pascual, Juan A Botía, Nicholas W Wood, Rita Horvath, Andreas M Ernst, James E Rothman, Meriel McEntagart, Yanick J Crow, Fowzan Sami Alkuraya, Gaël Nicolas, null null, Thomas Arnesen, Henry Houlden
Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications. Nature communications 15 (1) (2024)
Viorica Chelban, Henriette Aksnes, Reza Maroofian, Lauren C LaMonica, Luis Seabra, Anette Siggervåg, Perrine Devic, Hanan E Shamseldin, Jana Vandrovcova, David Murphy, Anne-Claire Richard, Olivier Quenez, Antoine Bonnevalle, M Natalia Zanetti, Rauan Kaiyrzhanov, Vincenzo Salpietro, Stephanie Efthymiou, Lucia V Schottlaender, Heba Morsy, Annarita Scardamaglia, Ambreen Tariq, Alistair T Pagnamenta, Ajia Pennavaria, Liv S Krogstad, Åse K Bekkelund, Alessia Caiella, Nina Glomnes, Kirsten M Brønstad, Sandrine Tury, Andrés Moreno De Luca, Anne Boland-Auge, Robert Olaso, Jean François Deleuze, Mathieu Anheim, Benjamin Cretin, Barbara Vona, Fahad S Al-Ajlan, Firdous Abdulwahab, Jean-Luc Battini, Rojan İpek, Peter Bauer, Giovanni Zifarelli, Serdal Gungor, Semra Hiz Kurul, Hanns Lochmüller, Sahar Isa Da'as, Khalid A Fakhro, Alicia Gómez-Pascual, Juan A Botía, Nicholas W Wood, Rita Horvath, Andreas M Ernst, James E Rothman, Meriel McEntagart, Yanick J Crow, Fowzan Sami Alkuraya, Gaël Nicolas, null null, Thomas Arnesen, Henry Houlden
Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications. Nature communications 15 (1) (2024)
Viorica Chelban, Henriette Aksnes, Reza Maroofian, Lauren C LaMonica, Luis Seabra, Anette Siggervåg, Perrine Devic, Hanan E Shamseldin, Jana Vandrovcova, David Murphy, Anne-Claire Richard, Olivier Quenez, Antoine Bonnevalle, M Natalia Zanetti, Rauan Kaiyrzhanov, Vincenzo Salpietro, Stephanie Efthymiou, Lucia V Schottlaender, Heba Morsy, Annarita Scardamaglia, Ambreen Tariq, Alistair T Pagnamenta, Ajia Pennavaria, Liv S Krogstad, Åse K Bekkelund, Alessia Caiella, Nina Glomnes, Kirsten M Brønstad, Sandrine Tury, Andrés Moreno De Luca, Anne Boland-Auge, Robert Olaso, Jean François Deleuze, Mathieu Anheim, Benjamin Cretin, Barbara Vona, Fahad S Al-Ajlan, Firdous Abdulwahab, Jean-Luc Battini, Rojan İpek, Peter Bauer, Giovanni Zifarelli, Serdal Gungor, Semra Hiz Kurul, Hanns Lochmüller, Sahar Isa Da'as, Khalid A Fakhro, Alicia Gómez-Pascual, Juan A Botía, Nicholas W Wood, Rita Horvath, Andreas M Ernst, James E Rothman, Meriel McEntagart, Yanick J Crow, Fowzan Sami Alkuraya, Gaël Nicolas, null null, Thomas Arnesen, Henry Houlden
Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications. Nature communications 15 (1) (2024)
Niccolò Rossi, Najeeb Syed, Alessia Visconti, Elbay Aliyev, Sarah Berry, Mafalda Bourbon, Tim D Spector, Pirro G Hysi, Khalid A Fakhro, Mario Falchi
Rare variants at KCNJ2 are associated with LDL-cholesterol levels in a cross-population study. NPJ genomic medicine 9 (1) (2024)
Rulan Shaath, Aljazi Al-Maraghi, Haytham Ali, Jehan AlRayahi, Adam D Kennedy, Karen L DeBalsi, Sura Hussein, Najwa Elbashir, Sujitha S Padmajeya, Sasirekha Palaniswamy, Sarah H Elsea, Ammira A Akil, Noha A Yousri, Khalid A Fakhro
Integrating Genome Sequencing and Untargeted Metabolomics in Monozygotic Twins with a Rare Complex Neurological Disorder. Metabolites 14 (3) (2024)
Niccolò Rossi, Najeeb Syed, Alessia Visconti, Elbay Aliyev, Sarah Berry, Mafalda Bourbon, Tim D Spector, Pirro G Hysi, Khalid A Fakhro, Mario Falchi
Rare variants at KCNJ2 are associated with LDL-cholesterol levels in a cross-population study. NPJ genomic medicine 9 (1) (2024)
Niccolò Rossi, Najeeb Syed, Alessia Visconti, Elbay Aliyev, Sarah Berry, Mafalda Bourbon, Tim D Spector, Pirro G Hysi, Khalid A Fakhro, Mario Falchi
Rare variants at KCNJ2 are associated with LDL-cholesterol levels in a cross-population study. NPJ genomic medicine 9 (1) (2024)
Waleed Aamer, Aljazi Al-Maraghi, Najeeb Syed, Geethanjali Devadoss Gandhi, Elbay Aliyev, Alya A Al-Kurbi, Omayma Al-Saei, Muhammad Kohailan, Navaneethakrishnan Krishnamoorthy, Sasirekha Palaniswamy, Khulod Al-Malki, Saleha Abbasi, Nourhen Agrebi, Fatemeh Abbaszadeh, Ammira S Al-Shabeeb Akil, Ramin Badii, Tawfeg Ben-Omran, Bernice Lo, null null, Younes Mokrab, Khalid A Fakhro
Burden of Mendelian disorders in a large Middle Eastern biobank. Genome medicine 16 (1) (2024)
Aisha Nasser J M Al-Saei, Wared Nour-Eldine, Kashif Rajpoot, Noman Arshad, Abeer R Al-Shammari, Madeeha Kamal, Ammira Al-Shabeeb Akil, Khalid A Fakhro, Paul J Thornalley, Naila Rabbani
Validation of plasma protein glycation and oxidation biomarkers for the diagnosis of autism. Molecular psychiatry 29 (3) (2023)
Aisha Nasser J M Al-Saei, Wared Nour-Eldine, Kashif Rajpoot, Noman Arshad, Abeer R Al-Shammari, Madeeha Kamal, Ammira Al-Shabeeb Akil, Khalid A Fakhro, Paul J Thornalley, Naila Rabbani
Validation of plasma protein glycation and oxidation biomarkers for the diagnosis of autism. Molecular psychiatry 29 (3) (2023)
Alya A Al-Kurbi, Elbay Aliyev, Sana AlSa'afin, Waleed Aamer, Sasirekha Palaniswamy, Aljazi Al-Maraghi, Houda Kilani, Ammira Al-Shabeeb Akil, Mitchell A Stotland, Khalid A Fakhro
A Complex Intrachromosomal Rearrangement Disrupting IRF6 in a Family with Popliteal Pterygium and Van der Woude Syndromes. Genes 14 (4) (2023)
Alya A Al-Kurbi, Elbay Aliyev, Sana AlSa'afin, Waleed Aamer, Sasirekha Palaniswamy, Aljazi Al-Maraghi, Houda Kilani, Ammira Al-Shabeeb Akil, Mitchell A Stotland, Khalid A Fakhro
A Complex Intrachromosomal Rearrangement Disrupting IRF6 in a Family with Popliteal Pterygium and Van der Woude Syndromes. Genes 14 (4) (2023)
Mona Abdi, Elbay Aliyev, Brett Trost, Muhammad Kohailan, Waleed Aamer, Najeeb Syed, Rulan Shaath, Geethanjali Devadoss Gandhi, Worrawat Engchuan, Jennifer Howe, Bhooma Thiruvahindrapuram, Melissa Geng, Joe Whitney, Amira Syed, Jyothi Lakshmi, Sura Hussein, Najwa Albashir, Amal Hussein, Ilaria Poggiolini, Saba F Elhag, Sasirekha Palaniswamy, Marios Kambouris, Maria de Fatima Janjua, Mohamed O El Tahir, Ahsan Nazeer, Durre Shahwar, Muhammad Waqar Azeem, Younes Mokrab, Nazim Abdel Aati, Ammira Akil, Stephen W Scherer, Madeeha Kamal, Khalid A Fakhro
Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study. Genome medicine 15 (1) (2023)
Alya A Al-Kurbi, Elbay Aliyev, Sana AlSa'afin, Waleed Aamer, Sasirekha Palaniswamy, Aljazi Al-Maraghi, Houda Kilani, Ammira Al-Shabeeb Akil, Mitchell A Stotland, Khalid A Fakhro
A Complex Intrachromosomal Rearrangement Disrupting IRF6 in a Family with Popliteal Pterygium and Van der Woude Syndromes. Genes 14 (4) (2023)
Aisha Nasser J M Al-Saei, Wared Nour-Eldine, Kashif Rajpoot, Noman Arshad, Abeer R Al-Shammari, Madeeha Kamal, Ammira Al-Shabeeb Akil, Khalid A Fakhro, Paul J Thornalley, Naila Rabbani
Validation of plasma protein glycation and oxidation biomarkers for the diagnosis of autism. Molecular psychiatry 29 (3) (2023)
Alya A Al-Kurbi, Elbay Aliyev, Sana AlSa'afin, Waleed Aamer, Sasirekha Palaniswamy, Aljazi Al-Maraghi, Houda Kilani, Ammira Al-Shabeeb Akil, Mitchell A Stotland, Khalid A Fakhro
A Complex Intrachromosomal Rearrangement Disrupting IRF6 in a Family with Popliteal Pterygium and Van der Woude Syndromes. Genes 14 (4) (2023)
Aisha Nasser J M Al-Saei, Wared Nour-Eldine, Kashif Rajpoot, Noman Arshad, Abeer R Al-Shammari, Madeeha Kamal, Ammira Al-Shabeeb Akil, Khalid A Fakhro, Paul J Thornalley, Naila Rabbani
Validation of plasma protein glycation and oxidation biomarkers for the diagnosis of autism. Molecular psychiatry 29 (3) (2023)
Aisha Nasser J M Al-Saei, Wared Nour-Eldine, Kashif Rajpoot, Noman Arshad, Abeer R Al-Shammari, Madeeha Kamal, Ammira Al-Shabeeb Akil, Khalid A Fakhro, Paul J Thornalley, Naila Rabbani
Validation of plasma protein glycation and oxidation biomarkers for the diagnosis of autism. Molecular psychiatry 29 (3) (2023)
Aisha Nasser J M Al-Saei, Wared Nour-Eldine, Kashif Rajpoot, Noman Arshad, Abeer R Al-Shammari, Madeeha Kamal, Ammira Al-Shabeeb Akil, Khalid A Fakhro, Paul J Thornalley, Naila Rabbani
Validation of plasma protein glycation and oxidation biomarkers for the diagnosis of autism. Molecular psychiatry (2023)
Sahar Isa Da'as, Waseem Hasan, Rola Salem, Nadin N Younes, Doua Abdelrahman, Iman A Mohamed, Arwa Aldaalis, Ramzi Temanni, Lisa Sara Mathew, Stephan Lorenz, Magdi Yacoub, Michail Nomikos, Gheyath K Nasrallah, Khalid A Fakhro
Transcriptome Profile Identifies Actin as an Essential Regulator of Cardiac Myosin Binding Protein C3 Hypertrophic Cardiomyopathy in a Zebrafish Model. International journal of molecular sciences 23 (16) (2022)
Muhammad Kohailan, Waleed Aamer, Najeeb Syed, Sujitha Padmajeya, Sura Hussein, Amira Sayed, Jyothi Janardhanan, Sasirekha Palaniswamy, Nady El Hajj, Ammira Al-Shabeeb Akil, Khalid A Fakhro
Patterns and distribution of de novo mutations in multiplex Middle Eastern families. Journal of human genetics 67 (10) (2022)
Senthil Selvaraj, Dírcea Rodrigues, Navaneethakrishnan Krishnamoorthy, Khalid A Fakhro, Luís R Saraiva, Manuel Carlos Lemos
Clinical, Genetic and Functional Characterization of a Novel AVPR2 Missense Mutation in a Woman with X-Linked Recessive Nephrogenic Diabetes Insipidus. Journal of personalized medicine 12 (1) (2022)
Geethanjali Devadoss Gandhi, Waleed Aamer, Navaneethakrishnan Krishnamoorthy, Najeeb Syed, Elbay Aliyev, Aljazi Al-Maraghi, Muhammad Kohailan, Jamil Alenbawi, Mohammed Elanbari, null null, Borbala Mifsud, Younes Mokrab, Charbel Abi Khalil, Khalid A Fakhro
Assessing the genetic burden of familial hypercholesterolemia in a large middle eastern biobank. Journal of translational medicine 20 (1) (2022)
Hamdi Mbarek, Geethanjali Devadoss Gandhi, Senthil Selvaraj, Wadha Al-Muftah, Radja Badji, Yasser Al-Sarraj, Chadi Saad, Dima Darwish, Muhammad Alvi, Tasnim Fadl, Heba Yasin, Fatima Alkuwari, Rozaimi B Mahamad Razali, Waleed Aamer, Fatemeh Abbaszadeh, Ikhlak Ahmed, Younes Mokrab, Karsten Suhre, Omar M E Albagha, Khalid A Fakhro, Ramin Badii, Said I Ismail, Asma Althani, null null
Qatar genome: Insights on genomics from the Middle East. Human mutation 43 (4) (2022)
Daniele Merico, Yehonatan Pasternak, Mehdi Zarrei, Edward J Higginbotham, Bhooma Thiruvahindrapuram, Ori Scott, Jessica Willett-Pachul, Eyal Grunebaum, Julia Upton, Adelle Atkinson, Vy H D Kim, Elbay Aliyev, Khalid A Fakhro, Stephen W Scherer, Chaim M Roifman
Homozygous duplication identified by whole genome sequencing causes LRBA deficiency. NPJ genomic medicine 6 (1) (2021)
Rozaimi Mohamad Razali, Juan Lorenzo Rodriguez-Flores, Mohammadmersad Ghorbani, Haroon Naeem, Waleed Aamer, Elbay Aliyev, Ali Jubran, null null, Andrew G Clark, Khalid A Fakhro, Younes Mokrab
Thousands of Qatari genomes inform human migration history and improve imputation of Arab haplotypes. Nature communications 12 (1) (2021)
Navaneethakrishnan Krishnamoorthy, Khalid A Fakhro
Identification of mutation resistance coldspots for targeting the SARS-CoV2 main protease. IUBMB life 73 (4) (2021)
Niccolo' Rossi, Elbay Aliyev, Alessia Visconti, Ammira S A Akil, Najeeb Syed, Waleed Aamer, Sujitha S Padmajeya, Mario Falchi, Khalid A Fakhro
Ethnic-specific association of amylase gene copy number with adiposity traits in a large Middle Eastern biobank. NPJ genomic medicine 6 (1) (2021)
Santosh K Yadav, Ajaz Ahmad Bhat, Sheema Hashem, Sabah Nisar, Madeeha Kamal, Najeeb Syed, Mohamed-Ramzi Temanni, Rakesh K Gupta, Saddat Kamran, Muhammad Waqar Azeem, Amit K Srivastava, Puneet Bagga, Sanjeev Chawla, Ravinder Reddy, Michael P Frenneaux, Khalid A Fakhro, Mohammad Haris
Genetic variations influence brain changes in patients with attention-deficit hyperactivity disorder. Translational psychiatry 11 (1) (2021)
Sahar I Da'as, Waleed Aamer, Waseem Hasan, Aljazi Al-Maraghi, Alya Al-Kurbi, Houda Kilani, Jehan AlRayahi, Khaled Zamel, Mitchell A Stotland, Khalid A Fakhro
PGAP3 Associated with Hyperphosphatasia with Mental Retardation Plays a Novel Role in Brain Morphogenesis and Neuronal Wiring at Early Development. Cells 9 (8) (2020)
Ammira-Sarah Al-Shabeeb Akil, Laila F Jerman, Esraa Yassin, Sujitha S Padmajeya, Alya Al-Kurbi, Khalid A Fakhro
Reading between the (Genetic) Lines: How Epigenetics is Unlocking Novel Therapies for Type 1 Diabetes. Cells 9 (11) (2020)
Sheema Hashem, Sabah Nisar, Ajaz Ahmad Bhat, Santosh Kumar Yadav, Muhammad Waqar Azeem, Puneet Bagga, Khalid A Fakhro, Ravinder Reddy, Michael P Frenneaux, Mohammad Haris
Genetics of structural and functional brain changes in autism spectrum disorder. Translational psychiatry 10 (1) (2020)
Hanan F Abdul Rahim, Said I Ismail, Amel Hassan, Tasnim Fadl, Salma M Khaled, Bethany Shockley, Catherine Nasrallah, Yara Qutteina, Engi Elmaghraby, Heba Yasin, Dima Darwish, Khalid A Fakhro, Radja Badji, Wadha Al-Muftah, Nahla Afifi, Asmaa Althani
Willingness to participate in genome testing: a survey of public attitudes from Qatar. Journal of human genetics 65 (12) (2020)

Khalid A Fakhro.css-eqlu8i{font-size:small;padding-left:4px;} (Khalid Fakhro)

Publication Activity (10 Years)

Top Topics

Top Venues

Khalid A Fakhro (Khalid Fakhro)