Saranya Suriyanarayanan

Author

University Hospital of Zurich ORCID

Also Known As

S. Suriyanarayanan, Saranya Suriyanarayanan, SuriyaNarayanan S., Suriyanarayanan, S, Suriyanarayanan, Saranya

Publications

579

Citations

H-Index

Concepts

All Affiliations

University Hospital of Zurich University of Zurich Swiss Integrative Center for Human Health Ludwig-Maximilians-Universität München University of Helsinki

About

Saranya Suriyanarayanan is an author at University Hospital of Zurich specializing in medicine, genetics, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	252
2	Molecular Genetics	3	3	133
3	Molecular Biology	2	2	112
4	Natural Sciences	1	1	88
5	Biochemistry	1	1	88

Saranya Suriyanarayanan

Publications

564

Citations

H-Index

Page 1

	Year	Citations
DEGS1-associated aberrant sphingolipid metabolism impairs nervous system function in humans Gergely Karsai, Florian Kraft, Natja Haag, Journal of Clinical Investigation	2019	127
Randomized trial of <scp>l</scp> -serine in patients with hereditary sensory and autonomic neuropathy type 1 Vera Fridman, Saranya Suriyanarayanan, Péter Novák, Neurology	2019	111
HSAN1 mutations in serine palmitoyltransferase reveal a close structure–function–phenotype relationship Heiko Bode, Florence Bourquin, Saranya Suriyanarayanan, Human Molecular Genetics Peripheral NeuropathyBiochemistryHsan1 MutationsNatural SciencesGenetics	2015	88
Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies Maike F. Dohrn, Nicola Glöckle, Lejla Mulahasanovic, Journal of Neurochemistry Hereditary NeuropathiesFrequent GenesGeneticsPathologyDisease Gene Identification	2017	77
1-Deoxysphingolipid-induced neurotoxicity involves N-methyl-d-aspartate receptor signaling Tanja Güntert, Pascal Hänggi, Alaa Othman, Neuropharmacology 1-Deoxysphingolipid-induced NeurotoxicityMedicineNeuropharmacologyNeuroprotectionPharmacology	2016	42
Clinical and metabolic consequences of L-serine supplementation in hereditary sensory and autonomic neuropathy type 1C Mari Auranen, Jussi Toppila, Saranya Suriyanarayanan, Molecular Case Studies	2017	34
Development of MRC Centre MRI calf muscle fat fraction protocol as a sensitive outcome measure in Hereditary Sensory Neuropathy Type 1 Umaiyal Kugathasan, Matthew R. Evans, Jasper M. Morrow, Journal of Neurology Neurosurgery & Psychiatry	2019	28
The Variant p.(Arg183Trp) in SPTLC2 Causes Late-Onset Hereditary Sensory Neuropathy Saranya Suriyanarayanan, Mari Auranen, Jussi Toppila, NeuroMolecular Medicine Molecular NeuroscienceVariant InterpretationGenetic DisorderGeneticsClinical Genetics	2015	24
A Novel Variant (Asn177Asp) in SPTLC2 Causing Hereditary Sensory Autonomic Neuropathy Type 1C Saranya Suriyanarayanan, Alaa Othman, Bianca Dräger, NeuroMolecular Medicine Novel VariantGenetic DisorderGeneticsPathologyDegenerative Disease	2019	21
Influence of self-assembling peptide nanofibre scaffolds on retinal differentiation potential of stem/progenitor cells derived from ciliary pigment epithelial cells Srilatha Jasty, Saranya Suriyanarayanan, Subramanian Krishnakumar Journal of Tissue Engineering and Regenerative Medicine	2014	12

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