Muhammad Zeeshan Anwar

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Bio

I am working in both clinical and academic positions simultaneously. I am flexible to work in any area whether it is academic or administrative. I mix in well with others and can communicate with people from different backgrounds. I work well as a team and on my own initiative. I see myself as a hardworking, honest, and reliable person who is committed to the care and welfare of others.

Research Interests

Papers共 198 篇Author StatisticsCo-AuthorSimilar Experts

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Biallelic Variants in BRF2 Are Associated with Craniofacial Anomalies and Cognitive Impairment

Anne Hebert, Sissy Bassani,Francesca Mattioli, Nazia Ibrahim, Flavia Palombo,Tommaso Pippucci, Nayereh Nouri, Marco Seri,Emily Farrow, Carol J. Sauders,Muhammad Ansar, Shagufta Naz, Alexandre Reymond

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 61-61

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IDENTIFICATION OF PREDISPOSING RISK FACTORS OF COVID-19 SEVERITY; A DESCRIPTIVE STUDY

Rana Muhammad Mateen,Muhammad Sohail Afzal,Sarmad Zahoor,Uzma Malik,Hafiz Muhammad Sajid Jehangir,Samara Siddique, Madiha Khalid,Imran Tipu,Ibrar Rafique,Muhammad Ansar,Rukhsana Parveen,Muhammad Arif Nadeem Saqib

Journal of Population Therapeutics and Clinical Pharmacology (2024)

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Next-generation Sequencing to Genetically Diagnose a Diverse Range of Inherited Eye Disorders in 15 Consanguineous Families from Pakistan

Rabia Basharat,Suzanne E. de Bruijn,Muhammad Zahid,Kim Rodenburg,Rebekkah J. Hitti-Malin,Maria Rodriguez-Hidalgo,Erica G. M. Boonen,Afeefa Jarral, Arif Mahmood,Jordi Corominas, Sharqa Khalil,Jawaid Ahmed Zai,Ghazanfar Ali,Javier Ruiz-Ederra,Christian Gilissen,Frans P. M. Cremers,Muhammad Ansar,Daan M. Panneman,Susanne Roosing

EXPERIMENTAL EYE RESEARCH (2024)

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Biallelic Variants in MRPL49 Cause Variable Clinical Presentations, Including Sensorineural Hearing Loss, Leukodystrophy, and Ovarian Insufficiency

Huw B Thomas,Leigh A M Demain,Alfredo Cabrera-Orefice, Isabelle Schrauwen,Hanan E Shamseldin, Alessandro Rea,Thashi Bharadwaj, Thomas B Smith,Monika Oláhová, Kyle Thompson,Langping He, Namanpreet Kaur,Anju Shukla, Musaad Abukhalid,Muhammad Ansar, Sakina Rehman, Saima Riazuddin,Firdous Abdulwahab, Janine M Smith,Zornitza Stark,Samantha Carrera, Wyatt W Yue,Kevin J Munro,Fowzan S Alkuraya, Peter Jamieson,Zubair M Ahmed,Suzanne M Leal,Robert W Taylor,Ilka Wittig, Raymond T O'Keefe,William G Newman

medRxiv the preprint server for health sciences (2024)

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Clinical and Genetic Investigation of 14 Families with Various Forms of Short Stature Syndromes

Fati Ullah Khan,Hammal Khan,Kifayat Ullah,Shoaib Nawaz,Muhammad Javed Khan,Sohail Ahmed,Muhammad Ilyas, Amjad Ali,Imran Ullah, Aamir Sohail,Shabir Hussain,Farooq Ahmad, Raza Sufyan,Amir Hayat, Tooba Hanif,Fatima Bibi, Maria Hayat, Rehmat Ullah, Inam Ullah Khan,Raja Hussain Ali,Muhammad Sharif Hasni,Hamid Ali,Muhammad Bilal,Susana Peralta,Rebecca Buchert,Zamrud Zehri, Gul Hassan, Khurrum Liaqat,Muhammad Zahid,Khadim Shah, Outi Mikitie,Tobias B. Haack,Weizhen Ji,Saquib A. Lakhani,Muhammad Ansar,Wasim Ahmad

CLINICAL GENETICSno. 3 (2024): 347-353

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Exploring the Pathological Mechanisms Underlying Cohen Syndrome

Fabrizio Vacca,Binnaz Yalcin,Muhammad Ansar

Frontiers in Neuroscience (2024)

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KIF1A Novel Frameshift Variant P.(ser887profs*64) Exhibits Clinical Heterogeneity in a Pakistani Family with Hereditary Sensory and Autonomic Neuropathy Type IIC

Saima Ghafoor,Muhammad Arshad Rafiq,Syed Tahir Abbas Shah,Muhammad Ansar,Tara Paton,Muhmmad Ajmal,Zehra Agha,Raheel Qamar,Maleeha Azam

INTERNATIONAL JOURNAL OF NEUROSCIENCEno. 6 (2024): 665-675

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Genome Sequencing Reveals Novel Causative Structural and Single Nucleotide Variants in Pakistani Families with Congenital Hypogonadotropic Hypogonadism

Yassine Zouaghi, Anbreen Mazhar Choudhary,Saba Irshad,Michela Adamo,Khaleeq ur Rehman,Ambrin Fatima, Mariam Shahid,Nida Najmi,Fernanda De Azevedo Correa,Imen Habibi,Alexia Boizot,Nicolas J. Niederländer,Muhammad Ansar,Federico Santoni,James Acierno,Nelly Pitteloud

BMC GENOMICSno. 1 (2024)

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Biallelic Variants in NSUN6 Cause an Autosomal Recessive Neurodevelopmental Disorder

Francesca Mattioli,Lina Worpenberg,Cai-Tao Li,Nazia Ibrahim,Shagufta Naz,Saima Sharif,Saghar Ghasemi Firouzabadi,Shohreh Vosoogh,Radoslava Saraeva-Lamri,Laure Raymond,Carlos Trujillo,Nicolas Guex,Stylianos Antonarakis,Muhammad Ansar,Hossein Darvish,Ru-Juan Liu,Jean-Yves Roignant,Alexandre Reymond

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 7-7

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The Genetic Cause of Neurodevelopmental Disorders in 30 Consanguineous Families

Sohail Aziz Paracha,Shoaib Nawaz,Muhammad Tahir Sarwar,Asmat Shaheen,Gohar Zaman,Jawad Ahmed, Fahim Shah, Sundus Khwaja,Abid Jan,Nida Khan,Mohammad Azhar Kamal,Qamre Alam,Safdar Abbas, Saman Farman, Ahmed Waqas,Afnan Alkathiri,Abdullah Hamadi,Federico Santoni,Naseeb Ullah, Bisma Khalid,Stylianos E. Antonarakis,Khalid A. Fakhro, Muhammad Umair,Muhammad Ansar

FRONTIERS IN MEDICINE (2024)

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Assisstant professor

Papers共 198 篇Author StatisticsCo-AuthorSimilar Experts