Atchayaram Nalini

4.8k citations

239 papers · 2.9k indexed · h-index 30

Neurology top 0.5%
- Amyotrophic Lateral Sclerosis Research 59
- Parkinson's Disease Mechanisms and Treatments 19
- Peripheral Neuropathies and Disorders 11
Genetics top 1%
- Neurogenetic and Muscular Disorders Research 54
Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases 17
Neurology top 5%
- Amyotrophic Lateral Sclerosis Research 59
- Parkinson's Disease Mechanisms and Treatments 19
- Peripheral Neuropathies and Disorders 11
Pathology and Forensic Medicine top 5%
Molecular Biology
- Muscle Physiology and Disorders 49
- Nuclear Structure and Function 12
Cardiology and Cardiovascular Medicine
- Cardiomyopathy and Myosin Studies 22

Co-authors: T.R. Raju M. Gourie‐Devi Narayanappa Gayathri Talakad N. Sathyaprabha Phalguni Anand Alladi K. Vijayalakshmi Seena Vengalil Kiran Polavarapu
Cited by: Neurology Genetics Cellular and Molecular Neuroscience
Partner nations: India Canada United States

In The Last Decade

Atchayaram Nalini

217 papers receiving 2.8k citations

Peers

Countries citing papers authored by Atchayaram Nalini

Since Specialization

Citations

This map shows the geographic impact of Atchayaram Nalini'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 Atchayaram Nalini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Atchayaram Nalini more than expected).

Fields of papers citing papers by Atchayaram Nalini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Atchayaram Nalini. 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 Atchayaram Nalini. The network helps show where Atchayaram Nalini may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Atchayaram Nalini, 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 Atchayaram Nalini Line = papers co-authored together Atchayaram Nalini links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Acute myeloneuropathy due to Glutaric aciduria-1: Expanding the phenotypic spectrum Dipti Baskar,Rita Christopher,Gautham Arunachal,Davuluri Durga Srinivas Anudeep,Ambati Mounika,TA Sangeeth,Kiran Polavarapu,BS Shalini,Tarachand Joshi,Sai Bhargava Sanka,Saraswati Nashi,Pritam Raja,Ravindranadh Mundlamuri Chowdary,Ravi Yadav,Atchayaram Nalini,Seena Vengalil	2025	0
2	A Multinational Study of Patient and Caregiver‐Reported Insights Into ADSS1 Myopathy Merve Koç Yekedüz,Yunjung Choi,Soo‐Hyun Kim,Raquel van Gool,Hanne van der Heijden,Lise Vrolix,Buket Sonbas Cobb,Seward B. Rutkove,Julie Shulman,Alan H. Beggs,Atchayaram Nalini,Dipti Baskar,Naveen Baweja,Priyanka Kakkar,Walla Al‐Hertani,Hyung Jun Park,Jaymin Upadhyay	2025	0
3	“Chocolate Chip Sign” on Susceptibility-Weighted Imaging Shoichiro Ando,Rie Saito,Sho Kitahara,Masahiro Uemura,Yuya Hatano,Masaki Watanabe,Taisuke Kato,Yosuke Ito,Atchayaram Nalini,Tomohiko Ishihara,Shigeo Murayama,Hironaka Igarashi,Akiyoshi Kakita,Osamu Onodera	2025	0
4	Low Complexity Model with Single Dimensional Feature for Speech Based Classification of Amyotrophic Lateral Sclerosis Patients and Healthy Individuals Anjali Jayakumar,Tanuka Bhattacharjee,Seena Vengalil,Yamini Belur,Atchayaram Nalini,Prasanta Kumar Ghosh	2024	0
5	Phenotype-Genotype Correlation of a Cohort of Patients with Congenital Myopathy: A Single Centre Experience from India Ganaraja Valakunja Harikrishna,Hansashree Padmanabha,Kiran Polavarapu,Ram Murthy Anjanappa,Veeramani Preethish‐Kumar,Bevinahalli N. Nandeesh,Seena Vengalil,‬Saraswati Nashi,Dipti Baskar,Aneesha Thomas,Mainak Bardhan,Gautham Arunachal,Deepak Menon,Sai Bhargava Sanka,N. Manjunath,Atchayaram Nalini	2024	1
6	Neuropalliative Care Needs Checklist for Motor Neuron Disease and Parkinson’s Disease: A Biopsychosocial Approach Lithin Zacharias,Priya Treesa Thomas,Manjusha G. Warrier,Ravi Yadav,Suvarna Alladi,Atchayaram Nalini,Pramod Kumar Pal	2024	0
7	Childhood-Onset Myopathy With Preserved Ambulation Caused by a Recurrent ADSSL1 Missense Variant Dipti Baskar,Kiran Polavarapu,Veeramani Preethish‐Kumar,Seena Vengalil,Saraswati Nashi,Ana Töpf,Aneesha Thomas,Sai Bhargava Sanka,Deepak Menon,Kosha Srivastava,Gautham Arunachal,Bevinahalli N. Nandeesh,Hanns Lochmüller,Atchayaram Nalini	2024	5
8	MYH2-related Myopathy: Expanding the Clinical Spectrum of Chronic Progressive External Ophthalmoplegia (CPEO) Dipti Baskar,Seena Vengalil,Saraswati Nashi,Mainak Bardhan,Kosha Srivastava,Sai Bhargava Sanka,Kiran Polavarapu,Deepak Menon,Veeramani Preethish‐Kumar,Hansashree Padmanabha,Gautham Arunachal,Atchayaram Nalini	2023	1
9	Resting heart rate variability as a diagnostic marker of cardiovascular dysautonomia in postural tachycardia syndrome Ganagarajan Inbaraj,Kaviraja Udupa,Prathyusha P. Vasuki,Atchayaram Nalini,Talakad N. Sathyaprabha	2022	5
10	A Novel L1 Linker Mutation in DES Resulted in Total Absence of Protein Rashmi Santhoshkumar,Veeramani Preethish‐Kumar,Kiran Polavarapu,Dinesh Reghunathan,Sima Chaudhari,Kapaettu Satyamoorthy,Seena Vengalil,Saraswati Nashi,Muhammed Faruq,Aditi Joshi,Atchayaram Nalini,Narayanappa Gayathri	2021	8
11	Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Mutations: The First Report from South Asia and Comprehensive Literature Review Kiran Polavarapu,Mainak Bardhan,Ram Murthy Anjanappa,Seena Vengalil,Veeramani Preethish‐Kumar,Leena Shingavi,Tanushree Chawla,Saraswati Nashi,Dhaarini Mohan,Gautham Arunachal,Thenral S. Geetha,Vedam L. Ramprasad,Atchayaram Nalini	2021	1
12	Muscle ultrasonography in detecting fasciculations: A noninvasive diagnostic tool for amyotrophic lateral sclerosis Rahul Reddy Rajula,Jitender Saini,Gopikrishnan Unnikrishnan,Seena Vengalil,Saraswati Nashi,Mainak Bardhan,Akshata Huddar,Tanushree Chawla,Dodmalur Malikarjuna Sindhu,Valakunja Harikrishna Ganaraja,Kiran Polavarapu,Veeramani Preethish‐Kumar,Kandavel Thennarasu,Atchayaram Nalini	2021	4
13	Recessive VAMP1 mutations associated with severe congenital myasthenic syndromes – A recognizable clinical phenotype Kiran Polavarapu,Seena Vengalil,Veeramani Preethish‐Kumar,Gautham Arunachal,Saraswati Nashi,Dhaarini Mohan,Tanushree Chawla,Mainak Bardhan,Bevinahalli N. Nandeesh,Priya Gupta,Vykuntaraju K. Gowda,Hanns Lochmüller,Atchayaram Nalini	2021	7
14	Diaphragmatic ultrasound: Prospects as a tool to assess respiratory muscle involvement in amyotrophic lateral sclerosis Rahul Reddy Rajula,Jitender Saini,Gopikrishnan Unnikrishnan,Seena Vengalil,Saraswati Nashi,Mainak Bardhan,Akshata Huddar,Tanushree Chawla,Dodmalur Mallikarjuna Sindhu,Valakunja Harikrishna Ganaraja,Kiran Polavarapu,Veeramani Preethish‐Kumar,Kandavel Thennarasu,Talakad N. Sathyaprabha,Atchayaram Nalini	2021	4
15	Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome Mainak Bardhan,Kiran Polavarapu,Nandeesh Bevinahalli,Veeramani Preethish‐Kumar,Ram Murthy Anjanappa,Gautham Arunachal,Leena Shingavi,Seena Vengalil,Saraswati Nashi,Tanushree Chawla,Divya Nagabushana,Dhaarini Mohan,Rita Horváth,Ichizo Nishino,Atchayaram Nalini	2021	8
16	Expanding the Phenotypic Spectrum of ECEL1-Associated Distal Arthrogryposis Akshata Huddar,Kiran Polavarapu,Veeramani Preethish‐Kumar,Mainak Bardhan,Gopikrishnan Unnikrishnan,Saraswati Nashi,Seena Vengalil,Priyanka Priyadarshini,Karthik Kulanthaivelu,Gautham Arunachal,Hanns Lochmüller,Atchayaram Nalini	2021	4
17	Whole‐exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations Shamita Sanga,Arnab Ghosh,Krishna Kumar,Kiran Polavarapu,Veeramani Preethish‐Kumar,Seena Vengalil,Saraswati Nashi,Mainak Bardhan,Gautham Arunachal,Sanita Raju,Narayanappa Gayathri,Nidhan K. Biswas,Saikat Chakrabarti,Atchayaram Nalini,Sudipto Roy,Moulinath Acharya	2020	9
18	MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India Sekar Deepha,Seena Vengalil,Veeramani Preethish‐Kumar,Kiran Polavarapu,Atchayaram Nalini,Narayanappa Gayathri,Meera Purushottam	2017	18
19	Proximal MR Neurography in Hansen’s Neuritis (P6.030) Manjunath Poojar,Ravinder Singh,Atchayaram Nalini,Jitender Saini,Anita Mahadevan,Veeranna Gadad	2015	1
20	Cortical Blindness As A Sequelae Of Horpes Simplex Encephalitis : A Case Report Atchayaram Nalini,Rangasetty Srinivasa,Acharya P.T	2000	0

About Atchayaram Nalini

Atchayaram Nalini is a scholar working on Neurology, Genetics and Cellular and Molecular Neuroscience, having authored 239 papers that have together received 2.9k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (59 papers), Neurogenetic and Muscular Disorders Research (54 papers), Muscle Physiology and Disorders (49 papers), Cardiomyopathy and Myosin Studies (22 papers), Parkinson's Disease Mechanisms and Treatments (19 papers), Genetic Neurodegenerative Diseases (17 papers), Nuclear Structure and Function (12 papers) and Peripheral Neuropathies and Disorders (11 papers). The work is most often cited by research in Neurology (1.3k citations), Genetics (642 citations) and Cellular and Molecular Neuroscience (625 citations). Atchayaram Nalini has collaborated with scholars based in India, Canada and United States. Frequent co-authors include T.R. Raju, M. Gourie‐Devi, Narayanappa Gayathri, Talakad N. Sathyaprabha, Phalguni Anand Alladi, K. Vijayalakshmi, Seena Vengalil, Kiran Polavarapu, Veeramani Preethish‐Kumar and Kandavel Thennarasu.

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