Mohammed Faruq (Mohd Faruq, M Faruq)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 36

Top Venues

Clinical genetics

Movement disorders : official journal of the Movement Disorder Society

Movement disorders clinical practice

Genes

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

Publications

Varun Suroliya, Bharathram Uppili, Manish Kumar, Vineet Jha, Achal K Srivastava, Mohammed Faruq
Identifying unstable CNG repeat loci in the human genome: a heuristic approach and implications for neurological disorders. Human genome variation 11 (1) (2024)
Bharathram Uppili, Mohammed Faruq
STRIDE-DB: a comprehensive database for exploration of instability and phenotypic relevance of short tandem repeats in the human genome. Database : the journal of biological databases and curation 2024 (2024)
Bharathram Uppili, Mohammed Faruq
STRIDE-DB: a comprehensive database for exploration of instability and phenotypic relevance of short tandem repeats in the human genome. Database : the journal of biological databases and curation 2024 (2024)
Divyani Garg, Himanshi Kapoor, Istaq Ahmad, Divya Goel, Sana Zahra, Pooja Sharma, Achal Kumar Srivastava, Mohammed Faruq
Cognitive Impairment, Ataxia, Dystonia, and Gaze Palsy Due to a Novel Variant in SQSTM1: New Lessons. Movement disorders : official journal of the Movement Disorder Society (2024)
Bharathram Uppili, Mohammed Faruq
STRIDE-DB: a comprehensive database for exploration of instability and phenotypic relevance of short tandem repeats in the human genome. Database : the journal of biological databases and curation 2024 (2024)
Varun Suroliya, Bharathram Uppili, Manish Kumar, Vineet Jha, Achal K Srivastava, Mohammed Faruq
Identifying unstable CNG repeat loci in the human genome: a heuristic approach and implications for neurological disorders. Human genome variation 11 (1) (2024)
Divyani Garg, Himanshi Kapoor, Istaq Ahmad, Divya Goel, Sana Zahra, Pooja Sharma, Achal Kumar Srivastava, Mohammed Faruq
Cognitive Impairment, Ataxia, Dystonia, and Gaze Palsy Due to a Novel Variant in SQSTM1: New Lessons. Movement disorders : official journal of the Movement Disorder Society 39 (2) (2024)
Varun Suroliya, Bharathram Uppili, Manish Kumar, Vineet Jha, Achal K Srivastava, Mohammed Faruq
Identifying unstable CNG repeat loci in the human genome: a heuristic approach and implications for neurological disorders. Human genome variation 11 (1) (2024)
Ayush Agarwal, Pooja Sharma, Divyani Garg, Jupita Handique, Akhilesh K Sonakar, Ajay Garg, Mohammed Faruq, Achal Kumar Srivastava
Founder SPG11 Mutation in the Baniya Community of India. Movement disorders : official journal of the Movement Disorder Society (2024)
Kana Ram Jat, Mohammed Faruq, Shishir Jindal, Shreya Bari, Akshita Soni, Pooja Sharma, Susi Mathews, Uzma Shamim, Vanshika Ahuja, Bharathram Uppilli, Subhash C Yadav, Rakesh Lodha, Sudheer K Arava, Sushil K Kabra
Genetics of 67 patients of suspected primary ciliary dyskinesia from India. Clinical genetics (2024)
Divyani Garg, Himanshi Kapoor, Istaq Ahmad, Divya Goel, Sana Zahra, Pooja Sharma, Achal Kumar Srivastava, Mohammed Faruq
Cognitive Impairment, Ataxia, Dystonia, and Gaze Palsy Due to a Novel Variant in SQSTM1: New Lessons. Movement disorders : official journal of the Movement Disorder Society 39 (2) (2024)
Kiran Narta, Manoj Ramesh Teltumbade, Mansi Vishal, Samreen Sadaf, Mohammed Faruq, Hodan Jama, Naushin Waseem, Aparna Rao, Abhijit Sen, Kunal Ray, Arijit Mukhopadhyay
Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration. Genes 14 (2) (2023)
Kiran Narta, Manoj Ramesh Teltumbade, Mansi Vishal, Samreen Sadaf, Mohammed Faruq, Hodan Jama, Naushin Waseem, Aparna Rao, Abhijit Sen, Kunal Ray, Arijit Mukhopadhyay
Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration. Genes 14 (2) (2023)
Manish Kumar, Nishu Tyagi, Mohammed Faruq
The molecular mechanisms of spinocerebellar ataxias for DNA repeat expansion in disease. Emerging topics in life sciences (2023)
Bharathram Uppili, Pooja Sharma, Istaq Ahmad, Shweta Sahni, Vivekanand Asokachandran, Anil B Nagaraja, Achal K Srivastava, Mohammed Faruq
Sequencing through hyperexpanded Friedreich's ataxia-GAA repeats by nanopore technology: implications in genotype-phenotype correlation. Brain communications 5 (2) (2023)
Kiran Narta, Manoj Ramesh Teltumbade, Mansi Vishal, Samreen Sadaf, Mohammed Faruq, Hodan Jama, Naushin Waseem, Aparna Rao, Abhijit Sen, Kunal Ray, Arijit Mukhopadhyay
Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration. Genes 14 (2) (2023)
Tsering Palmo, Bilal Ahmed Abbasi, Neha Chanana, Kavita Sharma, Mohammed Faruq, Tashi Thinlas, Malik Z Abdin, Qadar Pasha
The EDN1 Missense Variant rs5370 G > T Regulates Adaptation and Maladaptation under Hypobaric Hypoxia. International journal of environmental research and public health 19 (18) (2022)
Samhita Panda, Saksham Jain, Dhwani Dholakia, Bharath Ram Uppilli, Mohammed Faruq
Prolonged Episodic Dystonia in Tyrosine Hydroxylase Deficiency Due to Homozygous c.698G>A (p.Arg233His) Mutation-A Diagnostic Challenge. Movement disorders clinical practice 9 (8) (2022)
Pooja Sharma, Akhilesh Kumar Sonakar, Nishu Tyagi, Varun Suroliya, Manish Kumar, Rintu Kutum, Vivekananda Asokchandran, Sakshi Ambawat, Uzma Shamim, Avni Anand, Ishtaq Ahmad, Sunil Shakya, Bharathram Uppili, Aradhana Mathur, Shaista Parveen, Shweta Jain, Jyotsna Singh, Malika Seth, Sana Zahra, Aditi Joshi, Divya Goel, Shweta Sahni, Asangla Kamai, Saruchi Wadhwa, Aparna Murali, Sheeba Saifi, Debashish Chowdhury, Sanjay Pandey, Kuljeet Singh Anand, Ranganathan Lakshmi Narasimhan, Sanghamitra Laskar, Suman Kushwaha, Mukesh Kumar, Cheruvallill Velayudhan Shaji, Madakasira Vasantha Padma Srivastava, Achal K Srivastava, Mohammed Faruq, null null
Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening Tool. Advanced genetics (Hoboken, N.J.) 3 (2) (2022)
Pooja Sharma, Akhilesh Kumar Sonakar, Nishu Tyagi, Varun Suroliya, Manish Kumar, Rintu Kutum, Vivekananda Asokchandran, Sakshi Ambawat, Uzma Shamim, Avni Anand, Ishtaq Ahmad, Sunil Shakya, Bharathram Uppili, Aradhana Mathur, Shaista Parveen, Shweta Jain, Jyotsna Singh, Malika Seth, Sana Zahra, Aditi Joshi, Divya Goel, Shweta Sahni, Asangla Kamai, Saruchi Wadhwa, Aparna Murali, Sheeba Saifi, Debashish Chowdhury, Sanjay Pandey, Kuljeet Singh Anand, Ranganathan Lakshmi Narasimhan, Sanghamitra Laskar, Suman Kushwaha, Mukesh Kumar, Cheruvallill Velayudhan Shaji, Madakasira Vasantha Padma Srivastava, Achal K Srivastava, Mohammed Faruq, null null
Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening Tool. Advanced genetics (Hoboken, N.J.) 3 (2) (2022)
Divyani Garg, Sangeetha Yoganathan, Uzma Shamim, Kshitij Mankad, Parveen Gulati, Vincenzo Bonifati, Abhijeet Botre, Umesh Kalane, Arushi Gahlot Saini, Naveen Sankhyan, Kavita Srivastava, Vykuntaraju K Gowda, Monica Juneja, Mahesh Kamate, Hansashree Padmanabha, Debasis Panigrahi, Shaila Pachapure, Vrajesh Udani, Atin Kumar, Sanjay Pandey, Maya Thomas, Sumita Danda, Shaikh Atif Iqbalahmed, Annadurai Subramanian, Harish Pemde, Varinder Singh, Mohammed Faruq, Suvasini Sharma
Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian Children. Movement disorders clinical practice 9 (7) (2022)
Ankit K Pathak, Gyan Prakash Mishra, Bharathram Uppili, Safal Walia, Saman Fatihi, Tahseen Abbas, Sofia Banu, Arup Ghosh, Amol Kanampalliwar, Atimukta Jha, Sana Fatma, Shifu Aggarwal, Mahesh Shanker Dhar, Robin Marwal, Venkatraman Srinivasan Radhakrishnan, Kalaiarasan Ponnusamy, Sandhya Kabra, Partha Rakshit, Rahul C Bhoyar, Abhinav Jain, Mohit Kumar Divakar, Mohamed Imran, Mohammed Faruq, Divya Tej Sowpati, Lipi Thukral, Sunil K Raghav, Mitali Mukerji
Spatio-temporal dynamics of intra-host variability in SARS-CoV-2 genomes. Nucleic acids research 50 (3) (2022)
Ayush Agarwal, Rahul Oinam, Vinay Goel, Pooja Sharma, Mohammed Faruq, Ajay Garg, Achal Kumar Srivastava
"Ear of the Lynx" Sign in Hereditary Spastic Paraparesis (HSP) 76. Movement disorders clinical practice 10 (1) (2022)
Ayush Agarwal, Rahul Oinam, Vinay Goel, Pooja Sharma, Mohammed Faruq, Ajay Garg, Achal Kumar Srivastava
"Ear of the Lynx" Sign in Hereditary Spastic Paraparesis (HSP) 76. Movement disorders clinical practice 10 (1) (2022)
Mahesh S Dhar, Robin Marwal, Radhakrishnan Vs, Kalaiarasan Ponnusamy, Bani Jolly, Rahul C Bhoyar, Viren Sardana, Salwa Naushin, Mercy Rophina, Thomas A Mellan, Swapnil Mishra, Charles Whittaker, Saman Fatihi, Meena Datta, Priyanka Singh, Uma Sharma, Rajat Ujjainiya, Nitin Bhatheja, Mohit Kumar Divakar, Manoj K Singh, Mohamed Imran, Vigneshwar Senthivel, Ranjeet Maurya, Neha Jha, Priyanka Mehta, Vivekanand Asokachandran, Pooja Sharma, Arvinden Vr, Urmila Chaudhary, Namita Soni, Lipi Thukral, Seth R Flaxman, Samir Bhatt, Rajesh Pandey, Debasis Dash, Mohammed Faruq, Hemlata Lall, Hema Gogia, Preeti Madan, Sanket Kulkarni, Himanshu Chauhan, Shantanu Sengupta, Sandhya Kabra, null null, Ravindra Kumar Gupta, Sujeet K Singh, Anurag Agrawal, Partha Rakshit, Vinay Nandicoori, Karthik Bharadwaj Tallapaka, Divya Tej Sowpati, K Thangaraj, Murali Dharan Bashyam, Ashwin Dalal, Sridhar Sivasubbu, Vinod Scaria, Ajay Parida, Sunil K Raghav, Punit Prasad, Apurva Sarin, Satyajit Mayor, Uma Ramakrishnan, Dasaradhi Palakodeti, Aswin Sai Narain Seshasayee, Manoj Bhat, Yogesh Shouche, Ajay Pillai, Tanzin Dikid, Saumitra Das, Arindam Maitra, Sreedhar Chinnaswamy, Nidhan Kumar Biswas, Anita Sudhir Desai, Chitra Pattabiraman, M V Manjunatha, Reeta S Mani, Gautam Arunachal Udupi, Priya Abraham, Potdar Varsha Atul, Sarah S Cherian
Genomic characterization and epidemiology of an emerging SARS-CoV-2 variant in Delhi, India. Science (New York, N.Y.) 374 (6570) (2021)
Mahesh S Dhar, Vivekanand Asokachandran, Bharathram Uppili, Nishu Tyagi, Pooja Sharma, Simmi Tiwari, RadhaKrishnan V Srinivasan, Robin Marwal, Akshay Kanakan, Azka M Khan, Rajesh Pandey, Manoj Jais, Sanjib Gogoi, Ajit Shewale, Tushar Nale, Sandhya Kabra, Mohammed Faruq, Sujeet Singh, Anurag Agrawal, Partha Rakshit
Reinfection or reactivation: Genome-based two distinct SNP profile of SARS-CoV2 repositivity in an Indian case. Journal of medical virology 93 (7) (2021)
Pramod Kumar, Rajesh Pandey, Pooja Sharma, Mahesh S Dhar, Vivekanand A, Bharathram Uppili, Himanshu Vashisht, Saruchi Wadhwa, Nishu Tyagi, Saman Fatihi, Uma Sharma, Priyanka Singh, Hemlata Lall, Meena Datta, Poonam Gupta, Nidhi Saini, Aarti Tewari, Bibhash Nandi, Dhirendra Kumar, Satyabrata Bag, Deepanshi Gahlot, Surabhi Rathore, Nidhi Jatana, Varun Jaiswal, Hema Gogia, Preeti Madan, Simrita Singh, Prateek Singh, Debasis Dash, Manju Bala, Sandhya Kabra, Sujeet Singh, Mitali Mukerji, Lipi Thukral, Mohammed Faruq, Anurag Agrawal, Partha Rakshit
Integrated genomic view of SARS-CoV-2 in India. Wellcome open research 5 (2020)
Ankita Narang, Bharathram Uppilli, Asokachandran Vivekanand, Salwa Naushin, Arti Yadav, Khushboo Singhal, Uzma Shamim, Pooja Sharma, Sana Zahra, Aradhana Mathur, Malika Seth, Shaista Parveen, Archana Vats, Sara Hillman, Padma Dolma, Binuja Varma, Vandana Jain, null null, Bhavana Prasher, Shantanu Sengupta, Mitali Mukerji, Mohammed Faruq
Frequency spectrum of rare and clinically relevant markers in multiethnic Indian populations (ClinIndb): A resource for genomic medicine in India. Human mutation 41 (11) (2020)
Isha Panda, Istaq Ahmad, Shakti Sagar, Sana Zahra, Uzma Shamim, Suvasini Sharma, Mohammed Faruq
Encephalopathy due to defective mitochondrial and peroxisomal fission 2 caused by a novel MFF gene mutation in a young child. Clinical genetics 97 (6) (2020)
Radha Mahadevan, Rahul C Bhoyar, Natarajan Viswanathan, Raskin Erusan Rajagopal, Bobby Essaki, Varun Suroliya, Rachel Chelladurai, Saravanan Sankaralingam, Ganesan Shanmugam, Sriramakrishnan Vayanakkan, Uzma Shamim, Aradhana Mathur, Abhinav Jain, Mohamed Imran, Mohammed Faruq, Vinod Scaria, Sridhar Sivasubbu, Shantaraman Kalyanaraman
Genomic analysis of patients in a South Indian Community with autosomal dominant cortical tremor, myoclonus and epilepsy suggests a founder repeat expansion mutation in the SAMD12 gene. Brain communications 3 (1) (2020)
Mohammed Faruq, Deepak Kumar, Saruchi Wadhwa, Uzma Shamim, Aradhana Mathur, Shaista Parveen, Ajay Garg, Achal K Srivastava
Intrafamilial variable spastic paraplegia/ataxia/ALS phenotype linked to a novel KIF5A mutation. Clinical genetics 96 (3) (2019)
Sunil Shakya, Renu Kumari, Varun Suroliya, Nishu Tyagi, Aditi Joshi, Ajay Garg, Inder Singh, Divya Kalikavil Puthanveedu, Ajith Cherian, Mitali Mukerji, Achal K Srivastava, Mohammed Faruq
Whole exome and targeted gene sequencing to detect pathogenic recessive variants in early onset cerebellar ataxia. Clinical genetics 96 (6) (2019)
Monica Juneja, Uzma Shamim, Aditi Joshi, Aaradhna Mathur, Bharathram Uppili, Smitha Sairam, Sakshi Ambawat, Rashmi Dixit, Mohammed Faruq
A novel mutation in SLC39A14 causing hypermanganesemia associated with infantile onset dystonia. The journal of gene medicine 20 (4) (2018)
S K Vellarikkal, R Jayarajan, A Verma, R Ravi, V Senthilvel, A Kumar, L Saini, S Gulati, M Lal, A Mathur, M K Chhetri, Mohammed Faruq, Vinod Scaria, Sridhar Sivasubbu
A founder mutation MLC1 c.736delA associated with megalencephalic leukoencephalopathy with subcortical cysts-1 in north Indian kindred. Clinical genetics 94 (2) (2018)
Sweta Jain, Vamsee Chaitanya, Mohammed Faruq
A novel frameshift deletion in NAGLU causing sanfilipo type III-B in an Indian family. Clinical case reports 6 (12) (2018)
Mohammed Faruq, Jonathan J Magaña, Varun Suroliya, Ankita Narang, Nadia M Murillo-Melo, Oscar Hernández-Hernández, Achal K Srivastava, Mitali Mukerji
A Complete Association of an intronic SNP rs6798742 with Origin of Spinocerebellar Ataxia Type 7-CAG Expansion Loci in the Indian and Mexican Population. Annals of human genetics 81 (5) (2017)

Mohammed Faruq.css-eqlu8i{font-size:small;padding-left:4px;} (Mohd Faruq, M Faruq)

Publication Activity (10 Years)

Top Topics

Top Venues

Mohammed Faruq (Mohd Faruq, M Faruq)