Mohammed Faruq

2.2k citations

91 papers · 718 indexed · h-index 15

Cellular and Molecular Neuroscience top 10%
- Genetic Neurodegenerative Diseases 38
Genetics top 10%
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 5
- Glioma Diagnosis and Treatment 4
Neurology top 10%
- Neurological disorders and treatments 9
- Neurological diseases and metabolism 6
Neurology
- Neurological disorders and treatments 9
- Neurological diseases and metabolism 6
Molecular Biology
- Mitochondrial Function and Pathology 36
- DNA Repair Mechanisms 12

Co-authors: Achal Kumar Srivastava Vaishali Suri Pankaj Pathak Mehar Chand Sharma Chitra Sarkar Mitali Mukerji Ajay Garg Uzma Shamim
Cited by: Cellular and Molecular Neuroscience Genetics Neurology
Journals: SHILAP Revista de lepidopterología (2 papers)Brain (1 paper)Scientific Reports (2 papers)
Partner nations: India United States United Kingdom

In The Last Decade

Mohammed Faruq

80 papers receiving 711 citations

Peers

Countries citing papers authored by Mohammed Faruq

Since Specialization

Citations

This map shows the geographic impact of Mohammed Faruq's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Mohammed Faruq with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mohammed Faruq more than expected).

Fields of papers citing papers by Mohammed Faruq

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mohammed Faruq. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Mohammed Faruq. The network helps show where Mohammed Faruq may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Mohammed Faruq, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mohammed Faruq Line = papers co-authored together Mohammed Faruq links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Clinical utility of plasma cell-free DNA (cfDNA) in diffuse gliomas for the detection of IDH1 R132H mutation Pathology - Research and Practice ·Swati Singh,Supriya Bhardwaj,Iman Dandapath,Jyotsna Singh,Sumanta Das,Trishala Mohan,Santanu Kumar Bora,Shweta Kedia,Ashish Suri,Mehar Chand Sharma,Chitra Sarkar,Mohammed Faruq,Vaishali Suri	2024	0
2	Drug-refractory epilepsy due to a novel CLN5 mutation: A report of three patients from an Indian family Seizure ·Shiny Joy,Ayush Agarwal,Jupita Handique,Mahino Fatima,Divyani Garg,Pooja Sharma,Roopa Rajan,Ajay Garg,Mohammed Faruq,Achal Kumar Srivastava	2024	0
3	Genetics of 67 patients of suspected primary ciliary dyskinesia from India Clinical Genetics ·Kana Ram Jat,Mohammed Faruq,Shishir Jindal,Shreya Bari,Akshita Soni,Pooja Sharma,Susi Mathews,Uzma Shamim,Vanshika Ahuja,Bharathram Uppilli,Subhash Chandra Yadav,Rakesh Lodha,Sudheer Kumar Arava,Sushil Kumar Kabra	2024	0
4	Genetic and in silico analysis of Indian sporadic young onset patient with amyotrophic lateral sclerosis Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·Saileyee Roychowdhury,Deepika Joshi,Vinay Kumar Singh,Mohammed Faruq,Parimal Das	2024	0
5	Spectrum of Alport syndrome in an Indian cohort Pediatric Nephrology ·Menka Yadav,Trishla Jadon,Geetika Singh,Kshetrimayum Ghanapriya Devi,Monica Chandan,Priyanka Khandelwal,Jitendra Meena,Thenral S. Geetha,Mohammed Faruq,Pankaj Hari,Aditi Sinha,Arvind Bagga	2024	0
6	Co-occurrence of Parkinson’s disease and Retinitis Pigmentosa: A genetic and in silico analysis Neuroscience ·Archana Dwivedi,Anand Kumar,Mohammed Faruq,Varun Kumar Singh,Nidhi Dwivedi,Kamaljeet Singh,Ibrahim Hussain,Swati Parida,Girish Kumar Jha,Neeraj Kumar,Deepika Joshi	2024	2
7	Investigation of RFC1 tandem nucleotide repeat locus in diverse neurodegenerative outcomes in an Indian cohort Neurogenetics ·Nishu Tyagi,Bharathram Uppili,Pooja Sharma,Shaista Parveen,Sheeba Saifi,Abhinav Jain,Akhilesh Kumar Sonakar,Istaq Ahmed,Shweta Sahni,Uzma Shamim,Avni Anand,Varun Suroliya,A Vivekanand,Achal Kumar Srivastava,Sridhar Sivasubbu,Vinod Scaria,Mohammed Faruq	2023	4
8	Variants in complement genes are uncommon in patients with anti-factor H autoantibody-associated atypical hemolytic uremic syndrome Pediatric Nephrology ·Priyanka Khandelwal,Aditi Joshi,Aradhana Mathur,Mamta Puraswani,Bahadur Singh Gurjar,Aditi Sinha,Pankaj Hari,Mohammed Faruq,Arvind Bagga	2023	2
9	Widening the clinical, radiological and genetic spectrum of autosomal recessive ataxia of Charlevoix-Saguenay in Indian patients Acta Neurologica Belgica ·K. P. Divya,Ajith Cherian,(unknown),Savith Kumar,Bejoy Thomas,Mohammed Faruq	2023	1
10	Next Generation Sequencing and Cytogenetic Based Evaluation of Indian Pierre Robin Sequence Families Reveals CNV Regions of Modest Effect and a NovelLOXL3Mutation The Cleft Palate-Craniofacial Journal ·Anubhuti Sood,Uzma Shamim,Om Prakash Kharbanda,Madhulika Kabra,Neerja Gupta,Aradhana Mathur,Aditi Joshi,Shaista Parveen,Sana Zahra,Pooja Sharma,Malika Seth,Afreen Khan,Mohammed Faruq,Deepika Mishra	2021	2
11	Next-Generation Sequencing for Congenital Nephrotic Syndrome: A Multi-Center Cross-Sectional Study from India Indian Pediatrics ·Aditi Joshi,Aditi Sinha,Aakanksha Sharma,Uzma Shamim,Bharathram Uppilli,Pooja Sharma,Sana Zahra,Shaista Parveen,Aradhana Mathur,Monica Chandan,Prachi Tewari,Priyanka Khandelwal,Pankaj Hari,Mitali Mukerji,Mohammed Faruq,Arvind Bagga	2021	8
12	Encephalopathy due to defective mitochondrial and peroxisomal fission 2 caused by a novel MFF gene mutation in a young child Clinical Genetics ·Isha Panda,Istaq Ahmad,Shakti Sagar,Sana Zahra,Uzma Shamim,Suvasini Sharma,Mohammed Faruq	2020	18
13	Seven novel genetic variants in a North Indian cohort with classical homocystinuria Scientific Reports ·Rajdeep Kaur,Savita Verma Attri,Arushi Gahlot Saini,Naveen Sankhyan,Satwinder Singh,Mohammed Faruq,Vedam L. Ramprasad,Sheetal Sharda,Sakthivel Murugan	2020	6
14	Whole exome and targeted gene sequencing to detect pathogenic recessive variants in early onset cerebellar ataxia Clinical Genetics ·Sunil Shakya,Renu Kumari,Varun Suroliya,Nishu Tyagi,Aditi Joshi,Ajay Garg,Inder Singh,Divya Kalikavil Puthanveedu,Ajith Cherian,Mitali Mukerji,Achal Kumar Srivastava,Mohammed Faruq	2019	17
15	Spectrum of Pathogenic Variants in <b><i>SRD5A2</i></b> in Indian Children with 46,XY Disorders of Sex Development and Clinically Suspected Steroid 5α-Reductase 2 Deficiency Sexual Development ·Anil Kumar,Rajni Sharma,Mohammed Faruq,Varun Suroliya,Manoj Kumar,Shilpa Sharma,Ralf Werner,Olaf Hiort,Vandana Jain	2019	9
16	Loss of SMARCB1/INI1 Immunoexpression in Chordoid Meningiomas Neurology India ·MeharC Sharma,Prit Benny Malgulwar,Aanchal Kakkar,Ranajoy Ghosh,Pankaj Pathak,Chitra Sarkar,Vaishali Suri,Manmohan Singh,ShashankS Kale,Mohammed Faruq	2019	1
17	Genetic variations in olfactory receptor gene OR2AG2 in a large multigenerational family with asthma Scientific Reports ·Samarpana Chakraborty,Pushkar Dakle,Anirban Sinha,Sangeetha Vishweswaraiah,Aditya Nagori,Shivalingaswamy Salimath,Y. S. Prakash,Rakesh Lodha,S. K. Kabra,Balaram Ghosh,Mohammed Faruq,P A Mahesh,Anurag Agrawal	2019	11
18	Study of β-catenin and BRAF alterations in adamantinomatous and papillary craniopharyngiomas: mutation analysis with immunohistochemical correlation in 54 cases Journal of Neuro-Oncology ·Prit Benny Malgulwar,Aruna Nambirajan,Pankaj Pathak,Mohammed Faruq,Vaishali Suri,Chitra Sarkar,Amandeep Jagdevan,Bhawani Shankar Sharma,Mehar Chand Sharma	2017	19
19	Clinical behaviour of spinocerebellar ataxia type 12 and intermediate length abnormal CAG repeats inPPP2R2B Brain ·Achal Kumar Srivastava,Amit Takkar,Ajay Garg,Mohammed Faruq	2016	35
20	Prognostic value of MIB-1, p53, epidermal growth factor receptor, and INI1 in childhood chordomas Neuro-Oncology ·Rajni Yadav,Mehar Chand Sharma,Prit Benny Malgulwar,Pankaj Pathak,E. Sigamani,Vaishali Suri,Chiranjit Sarkar,Amandeep Kumar,Manmohan Singh,Bhawani S. Sharma,Ajay Garg,Sameer Bakhshi,Mohammed Faruq	2013	48

About Mohammed Faruq

Mohammed Faruq is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology, having authored 91 papers that have together received 718 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (38 papers), Mitochondrial Function and Pathology (36 papers), DNA Repair Mechanisms (12 papers), Neurological disorders and treatments (9 papers), Genetics and Neurodevelopmental Disorders (7 papers), Neurological diseases and metabolism (6 papers), Genomics and Rare Diseases (5 papers) and Glioma Diagnosis and Treatment (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (259 citations), Genetics (123 citations) and Neurology (163 citations). Mohammed Faruq has collaborated with scholars based in India, United States and United Kingdom. Frequent co-authors include Achal Kumar Srivastava, Vaishali Suri, Pankaj Pathak, Mehar Chand Sharma, Chitra Sarkar, Mitali Mukerji, Ajay Garg, Uzma Shamim, Prit Benny Malgulwar and Prerana Jha. Their work appears in journals such as SHILAP Revista de lepidopterología, Brain and Scientific Reports.

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