Mohnish Suri

7.6k citations

83 papers · 2.2k · 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
- Connective tissue disorders research
- Genomics and Rare Diseases

Papers in

Molecular Biology 37
- DNA Repair Mechanisms 7
- RNA regulation and disease 4
Genetics 30
- Genomic variations and chromosomal abnormalities 9
- Connective tissue disorders research 9
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 5
- Genetic Syndromes and Imprinting 5

Co-authors: Pradeep Vasudevan (3 shared papers)Jane Ravenscroft (2 shared papers)Ruth Newbury‐Ecob (3 shared papers)John Kendrick‐Jones (2 shared papers)Charles E. Schwartz (2 shared papers)Éva Morava (2 shared papers)Andrew O.M. Wilkie (2 shared papers)Abhijit Dixit (7 shared papers)
Journals: Developmental Medicine & Child Neurology (3 papers)Orphanet Journal of Rare Diseases (3 papers)European Journal of Paediatric Neurology (3 papers)Archives of Disease in Childhood (3 papers)Advances in 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-authors

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

Showing the 20 most-cited of 83 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	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	298
2	Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosis Proceedings of the National Academy of Sciences ·Vasyl Nesin, Graham B. Wiley, Maria Kousi, E‐Ching Ong, Thomas Lehmann, David Nicholl, Mohnish Suri, Nortina Shahrizaila, Nicholas Katsanis, Patrick M. Gaffney, Klaas J. Wierenga, Leonidas Tsiokas	2014	187
3	Mutation Analysis of Core Binding Factor A1 in Patients with Cleidocranial Dysplasia The American Journal of Human Genetics ·Ivo Quack, Birgitta Vonderstraß, Michael Stock, A.S Aylsworth, Achim Becker, L A Brueton, Peter J. Lee, F. Majewski, JB Mulliken, Mohnish Suri, Martin Zenker, Stefan Mundlos, F Otto	1999	172
4	A novel recurrent mutation in ATP1A3 causes CAPOS syndrome Orphanet Journal of Rare Diseases ·Michelle Demos, Clara DM van Karnebeek, Colin J.D. Ross, Shelin Adam, Yaoqing Shen, Shing H. Zhan, Casper Shyr, Gabriella Horváth, Mohnish Suri, Alan Fryer, Steven J.M. Jones, Jan M. Friedman	2014	137
5	Autosomal dominant inheritance of a heterozygous mutation in SAMHD1 causing familial chilblain lupus American Journal of Medical Genetics Part A ·Jane Ravenscroft, Mohnish Suri, Gillian Rice, Marcin Szynkiewicz, Yanick J. Crow	2010	88
6	Identification of the First ATRIP–Deficient Patient and Novel Mutations in ATR Define a Clinical Spectrum for ATR–ATRIP Seckel Syndrome PLoS Genetics ·Tomoo Ogi, Sarah Walker, Tom Stiff, Emma Hobson, Siripan Limsirichaikul, Gillian Carpenter, Katrina Prescott, Mohnish Suri, Philip J. Byrd, Michiko Matsuse, Norisato Mitsutake, Yuka Nakazawa, Pradeep Vasudevan, Margaret Barrow, Grant S. Stewart, A. Malcolm R. Taylor, Mark O’Driscoll, Penny A. Jeggo	2012	79
7	A clinical approach to developmental delay and intellectual disability Clinical Medicine ·Pradeep Vasudevan, Mohnish Suri	2017	73
8	Genetic Heterogeneity and Clinical Variability in Musculocontractural Ehlers-Danlos Syndrome Caused by Impaired Dermatan Sulfate Biosynthesis Human Mutation ·Delfien Syx, Tim Van Damme, Sofie Symoens, Merel Maiburg, Ingrid M.B.H. van de Laar, Jenny Morton, Mohnish Suri, Miguel Del Campo, Ingrid Haußer, Trinh Hermanns‐Lê, Anne De Paepe, Fransiska Malfait	2015	64
9	Pseudohypoparathyroidism Type 1b due to Paternal Uniparental Disomy of Chromosome 20q The Journal of Clinical Endocrinology & Metabolism ·Abhijit Dixit, Kate Chandler, Margaret Lever, Rebecca Poole, H. Bullman, M.Z. Mughal, Margaret Steggall, Mohnish Suri	2012	61
10	Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans European Journal of Human Genetics ·A. Gulhan Ercan‐Sencicek, Samira Jambi, Daniel Franjic, S. Nishimura, Mingfeng Li, Paul El-Fishawy, Thomas M. Morgan, Stephan Sanders, Kaya Bilgüvar, Mohnish Suri, Michele H. Johnson, Abha R. Gupta, Zafer Yüksel, Shrikant Mane, Elena L. Grigorenko, Marina R. Picciotto, Arthur S. Alberts, Murat Günel, Nenad Šestan, Matthew W. State	2014	56
11	Genotype, extrapyramidal features, and severity of variant ataxia‐telangiectasia Annals of Neurology ·Katherine Schon, Nienke J.H. van Os, Nicholas Oscroft, Helen Baxendale, Daniel Scoffings, Julian Ray, Mohnish Suri, William Whitehouse, Puja R. Mehta, Natasha Everett, Leonardo Bottolo, Bart P.C. van de Warrenburg, Philip J. Byrd, Corry M.R. Weemaes, Michèl A.A.P. Willemsen, Marc Tischkowitz, A. Malcolm R. Taylor, Anke Hensiek	2018	55
12	WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations American Journal of Medical Genetics Part A ·Mohnish Suri, P. Kelehan, David O’Neill, S. Vadeyar, Judith Grant, S. Faisal Ahmed, John Tolmie, Emma McCann, Wayne Lam, Shirley I. Smith, David Fitzpatrick, Nicholas D. Hastie, William Reardon	2007	50
13	Brittle cornea syndrome: recognition, molecular diagnosis and management Orphanet Journal of Rare Diseases ·Emma Mm Burkitt Wright, Louise F. Porter, Helen Spencer, Jill Clayton‐Smith, Leon Au, Francis L. Munier, Sarah Smithson, Mohnish Suri, Marianne Rohrbach, Forbes Manson, Graeme C. Black	2013	47
14	Clinical and radiographic findings in multiple epiphyseal dysplasia caused by MATN3 mutations: Description of 12 patients American Journal of Medical Genetics Part A ·Outi Mäkitie, Geert Mortier, Malwina Czarny‐Ratajczak, Michael Wright, Mohnish Suri, Piotr Rogala, M. Freund, Gail C. Jackson, Eveliina Jakkula, Leena Ala‐Kokko, Michael D. Briggs, William G. Cole	2003	45
15	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
16	17q12 microdeletion syndrome: Three patients illustrating the phenotypic spectrum American Journal of Medical Genetics Part A ·Abhijit Dixit, Chirag Patel, Rachel Harrison, Joanna Jarvis, Sally A. Hulton, Nigel Smith, Katherine Yates, Lee Silcock, Dominic McMullan, Mohnish Suri	2012	37
17	7q11.23 Microduplication: a recognizable phenotype Clinical Genetics ·Abhijit Dixit, Shane McKee, Sahar Mansour, SG Mehta, George A. Tanteles, Violetta Anastasiadou, PC Patsalis, Katherine Martin, Simon McCullough, Mohnish Suri, Ajoy Sarkar	2012	37
18	Homozygous Loss-of-Function Mutations in AP1B1, Encoding Beta-1 Subunit of Adaptor-Related Protein Complex 1, Cause MEDNIK-like Syndrome The American Journal of Human Genetics ·Hessa S. Alsaif, Mohammad Al-Owain, Martin E. Barrios‐Llerena, Ghada Gosadi, Yousef Binamer, David Devadason, Jane Ravenscroft, Mohnish Suri, Fowzan S. Alkuraya	2019	37
19	Rubinstein–Taybi syndrome type 2: report of nine new cases that extend the phenotypic and genotypic spectrum Clinical Dysmorphology ·Mark Hamilton, Ruth Newbury‐Ecob, Muriel Holder‐Espinasse, Shu Yau, Suzanne Lillis, Jane A. Hurst, Emma Clement, William Reardon, Shelagh Joss, Emma Hobson, Moira Blyth, Maryam Al-Shehhi, Sally Ann Lynch, Mohnish Suri	2016	36
20	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) ·Sp Robertson, Twigg, AJ Sutherland-Smith, Biancalana, R J Gorlin, David Horn, SJ Kenwrick, Kim CA, Éva Morava, Ruth Newbury‐Ecob, Orstavik Kh, OW Quarrell, CE Schwartz, Dj Shears, Mohnish Suri, John Kendrick‐Jones, Andrew O.M. Wilkie	2003	34

About Mohnish Suri

Mohnish Suri is a scholar working on Molecular Biology, Genetics, Cell Biology, Rheumatology and Surgery, having authored 83 papers that have together received 2.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Connective tissue disorders research (9 papers), DNA Repair Mechanisms (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Cellular transport and secretion (5 papers), Genomics and Rare Diseases (5 papers), Genetic Syndromes and Imprinting (5 papers) and RNA regulation and disease (4 papers). The work is most often cited by research in Sensory Systems (159 citations), Genetics (650 citations), Molecular Biology (1.1k citations), Cell Biology (239 citations) and Cellular and Molecular Neuroscience (195 citations). Mohnish Suri has collaborated with scholars based in United Kingdom, India and United States. Frequent co-authors include Pradeep Vasudevan, Jane Ravenscroft, Ruth Newbury‐Ecob, John Kendrick‐Jones, Charles E. Schwartz, Éva Morava, Andrew O.M. Wilkie, Abhijit Dixit, Valérie Biancalana and Mark Hamilton. Their work appears in journals such as Developmental Medicine & Child Neurology, Orphanet Journal of Rare Diseases, European Journal of Paediatric Neurology, Archives of Disease in Childhood and Advances in 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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Mohnish Suri

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Mohnish Suri

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About Mohnish Suri

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