Mohnish Suri

7.4k citations

82 papers · 2.2k indexed · h-index 24

Impact in

Sensory Systems top 2%
- Ion Channels and Receptors
Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Connective tissue disorders research

Papers in

Genetics 33
- Connective tissue disorders research 9
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 9
- Genomics and Rare Diseases 8
- Genetic Syndromes and Imprinting 5
Developmental Biology 2

Co-authors: Pradeep Vasudevan Ruth Newbury‐Ecob Jane Ravenscroft Charles E. Schwartz Andrew O.M. Wilkie Abhijit Dixit John Kendrick‐Jones Éva Morava
Journals: Orphanet Journal of Rare Diseases (3 papers)Developmental Medicine & Child Neurology (3 papers)European Journal of Paediatric Neurology (3 papers)Archives of Disease in Childhood (3 papers)The American Journal of Human Genetics (2 papers)
Partner nations: United Kingdom India United States

In The Last Decade

Mohnish Suri

80 papers receiving 2.1k citations

Peers

Countries citing papers authored by Mohnish Suri

Since Specialization

Citations

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

Fields of papers citing papers by Mohnish Suri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Pathogenic FLNA variants affecting the hinge region of filamin A are associated with male survival American Journal of Medical Genetics Part A ·清水圭一, Tim Morgan, Grégory Gimenez, Zandra A. Jenkins, Hannah Titheradge, Marie O’Donnell, David Skidmore, Mohnish Suri, Stephen P. Robertson	2024	0
2	Whole‐body MRI for cancer surveillance in ataxia–telangiectasia: A qualitative study of the perspectives of people affected by A‐T and their families Health Expectations ·Huanxiao Shi, Ja’far Isfahani, Brian Hu, J HOLLAND, Rafał Panek, Sophie Wilne, Mohnish Suri, William Whitehouse, FEDERICO CUEVAS-PÉREZ, Madhumita Dandapani, Robert A. Dineen, Cris Glazebrook	2023	4
3	Traboulsi syndrome caused by mutations in ASPH: An autosomal recessive disorder with overlapping features of Marfan syndrome European Journal of Medical Genetics ·Gabriela Jones, Sandra Trianadewi Lucin, Jacqueline Eason, Mark Hamilton, Deborah Osio, Nae-Yeou Jih, Júlia Baptista, Mohnish Suri	2022	10
4	Novel missense ACAN gene variants linked to familial osteochondritis dissecans cluster in the C-terminal globular domain of aggrecan Scientific Reports ·Eva‐Lena Stattin, Karin Lindblom, André Struglics, Patrik Önnerfjord, Jack Goldblatt, Abhijit Dixit, Ajoy Sarkar, Tabitha Randell, Mohnish Suri, Cathleen Raggio, Jessica G. Davis, Erin Carter, Anders Aspberg	2022	7
5	Maintenance Intravenous Immunoglobulin Treatment for Multiple Sclerosis Coexisting with Ehlers-Danlos Syndrome and Muir-Torre Syndrome: A Case Study Neurology and Therapy ·de Branco Fm, Mohnish Suri, Cris S. Constantinescu	2020	1
6	Exploring the genetic basis of 3MC syndrome: Findings in 12 further families American Journal of Medical Genetics Part A ·Jill Urquhart, R. C. Roberts, Kai Wang, Stavit A. Shalev, 実加納, Sheela Nampoothiri, Yves Sznajer, Nicole Revençu, علي عوض آل قطب, Mohnish Suri, Jamie M. Ellingford, Simon G. Williams, Sanjeev S. Bhaskar, Jill Clayton‐Smith	2016	22
7	Approach to the Diagnosis of Overgrowth Syndromes The Indian Journal of Pediatrics ·Mohnish Suri	2015	2
8	An emerging phenotype of Xq22 microdeletions in females with severe intellectual disability, hypotonia and behavioral abnormalities Journal of Human Genetics ·Toshiyuki Yamamoto, Anna Wilsdon, Shelagh Joss, Bertrand Isidor, Anna Erlandsson, Mohnish Suri, Noriko Sangu, Shino Shimada, Keiko Shimojima, Cédric Le Caignec, Lena Samuelsson, M Stefanova	2014	38
9	Denys–Drash syndrome and gonadoblastoma in a patient with Klinefelter syndrome Clinical Dysmorphology ·George A. Tanteles, Susan H. Oakley, Martin Christian, D.H. O’Neill, Mohnish Suri	2011	4
10	The phenotypic spectrum of ARX mutations Developmental Medicine & Child Neurology ·Mohnish Suri	2007	9
11	A presenilin 1 mutation (Arg278Ser) associated with early onset Alzheimer’s disease and spastic paraparesis Journal of the Neurological Sciences ·Ashok Raman, Xia Lin, Mohnish Suri, N. Yorifuji, Cris S. Constantinescu, Margaret Phillips	2007	12
12	Novel CDH3 mutations in hypotrichosis with juvenile macular dystrophy Clinical and Experimental Dermatology ·L. A. Aribisala, M Foglia, Marybeth Hummel, A Gagern, Mohnish Suri, Mohammad Khan, Marvin Bayne, Frank Schwartz, Eli Sprecher	2007	26
13	A microdeletion in Xp11.3 accounts for co‐segregation of retinitis pigmentosa and mental retardation in a large kindred American Journal of Medical Genetics Part A ·Lilei Zhang, Shesilia Putri Deani, Alan F. Wright, Mohnish Suri, Charles E. Schwartz, Roger E. Stevenson, David Valle	2006	19
14	L-2-hydroxyglutaric aciduria: novel mutations in the L-2-hydroxyglutarate dehydrogenase gene Journal of Inherited Metabolic Disease ·まなびあテラス, Shu min He, Nelida Jeanette Sánchez Ramos, Nasrin Mohassel Akhlaghi, Antònia Ribes, G. R. Voots, Tran Quoc Toan, Bernd A. Neubauer, Stanley H. Korman, Till Rümenapf, Yeswanth Akula, Hui-qin Tao, S H Seyedi, Vishnu Hegde, Christine Vianey‐Saban, Dimitrios Zafeiriou, Mohnish Suri, Reschi Dwi Fitri, S H Cook, C. Jakobs	2005	1
15	OPD-spectrum Disorders Clinical Collaborative Group. Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans Lirias (KU Leuven) ·季志忠, N. Gaillard, Alejandro Garofali Acosta, Andi Astuti Wulandari, R J Gorlin, David Horn, Belialova Ns, Merry Susanti Jonathan Suhanto, Éva Morava, Ruth Newbury‐Ecob, Wei Chen, Dunya Habash, CE Schwartz, Shaily Bhardwaj, Mohnish Suri, John Kendrick‐Jones, Andrew O.M. Wilkie	2003	34
16	What's new in Neurogenetics? Focus on ‘primary microcephaly’ European Journal of Paediatric Neurology ·Mohnish Suri	2003	5
17	Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans Nature Genetics ·Stephen P. Robertson, Stephen R.F. Twigg, Andrew J. Sutherland‐Smith, Valérie Biancalana, Robert J. Gorlin, Denise Horn, Susan Kenwrick, Chong Ae Kim, Éva Morava, Ruth Newbury‐Ecob, Karen Helene Ørstavik, Oliver Quarrell, Charles E. Schwartz, Deborah Shears, Mohnish Suri, John Kendrick‐Jones, Andrew O.M. Wilkie	2003	297
18	What's new in … neurogenetics? Focus on neurodegenerative disorders European Journal of Paediatric Neurology ·Mohnish Suri	2001	1
19	A profile of childhood neurocysticercosis The Indian Journal of Pediatrics ·关晶, Mohnish Suri, B. L. Jailkhani	1994	11
20	Thin ribs, thin tubular bones, abnormal facies and intrauterine growth retardation: a lethal syndrome British Journal of Radiology ·Mervyn Elliott, 熊宪光, K Saito, S Thirupuram, Mohnish Suri	1990	1

About Mohnish Suri

Mohnish Suri is a scholar working on Genetics, Developmental Biology, Molecular Biology, Cell Biology and Rheumatology, having authored 82 papers that have together received 2.2k indexed citations. Recurring topics across this work include Connective tissue disorders research (9 papers), Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (9 papers), Genomics and Rare Diseases (8 papers), DNA Repair Mechanisms (8 papers), Cellular transport and secretion (6 papers), Genetic Syndromes and Imprinting (5 papers) and Folate and B Vitamins Research (5 papers). The work is most often cited by research in Sensory Systems (158 citations), Genetics (736 citations), Molecular Biology (1.2k citations), Cell Biology (260 citations) and Developmental Biology (28 citations). Mohnish Suri has collaborated with scholars based in United Kingdom, India and United States. Frequent co-authors include Pradeep Vasudevan, Ruth Newbury‐Ecob, Jane Ravenscroft, Charles E. Schwartz, Andrew O.M. Wilkie, Abhijit Dixit, John Kendrick‐Jones, Éva Morava, Mark Hamilton and Marcin Szynkiewicz. Their work appears in journals such as Orphanet Journal of Rare Diseases, Developmental Medicine & Child Neurology, European Journal of Paediatric Neurology, Archives of Disease in Childhood and The American Journal of Human Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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