S
Sneh Lata
Researcher at Celgene
Publications - 32
Citations - 1433
Sneh Lata is an academic researcher from Celgene. The author has contributed to research in topics: Biology & Engineering. The author has an hindex of 12, co-authored 17 publications receiving 1163 citations. Previous affiliations of Sneh Lata include Columbia University & Bristol-Myers Squibb.
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Journal ArticleDOI
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
Krzysztof Kiryluk,Yifu Li,Francesco Scolari,Simone Sanna-Cherchi,Murim Choi,Miguel Verbitsky,David Fasel,Sneh Lata,Sindhuri Prakash,Samantha Shapiro,Clara Fischman,Holly J. Snyder,Gerald B. Appel,Claudia Izzi,Battista Fabio Viola,Nadia Dallera,Lucia Del Vecchio,Cristina Barlassina,Erika Salvi,Francesca Bertinetto,Antonio Amoroso,Silvana Savoldi,Marcella Rocchietti,Alessandro Amore,Licia Peruzzi,Rosanna Coppo,Maurizio Salvadori,Pietro Ravani,Riccardo Magistroni,Gian Marco Ghiggeri,Gianluca Caridi,Monica Bodria,Francesca Lugani,Landino Allegri,Marco Delsante,Mariarosa Maiorana,Andrea Magnano,Giovanni M. Frascà,Emanuela Boer,Giuliano Boscutti,Claudio Ponticelli,Renzo Mignani,Carmelita Marcantoni,Domenico Di Landro,Domenico Santoro,Antonello Pani,Rosaria Polci,Sandro Feriozzi,Silvana Chicca,Marco Galliani,Maddalena Gigante,Loreto Gesualdo,Pasquale Zamboli,Giovanni Giorgio Battaglia,Maurizio Garozzo,Dita Maixnerova,Vladimir Tesar,Frank Eitner,Thomas Rauen,Jürgen Floege,Tibor Kovács,Judit Nagy,Krzysztof Mucha,Leszek Pączek,Marcin Zaniew,Małgorzata Mizerska-Wasiak,Maria Roszkowska-Blaim,Krzysztof Pawlaczyk,Daniel P. Gale,Jonathan Barratt,Lise Thibaudin,François Berthoux,Guillaume Canaud,Anne Boland,Marie Metzger,Ulf Panzer,Hitoshi Suzuki,Shin Goto,Ichiei Narita,Yasar Caliskan,Jingyuan Xie,Ping Hou,Nan Chen,Hong Zhang,Robert J. Wyatt,Jan Novak,Bruce A. Julian,John Feehally,Bénédicte Stengel,Daniele Cusi,Richard P. Lifton,Ali G. Gharavi +91 more
TL;DR: A genome-wide association study of IgA nephropathy (IgAN), the most common form of glomerulonephritis, with discovery and follow-up in 20,612 individuals of European and East Asian ancestry is performed, suggesting a possible role for host–intestinal pathogen interactions in shaping the genetic landscape of IgAN.
Journal ArticleDOI
Analysis and prediction of antibacterial peptides
TL;DR: There is preference for certain residues at N and C termini, which helps to demarcate them from non-antibacterial peptides, which the authors hope will prove to be a boon to combat the dreadful antibiotic resistant bacteria.
Journal ArticleDOI
AntiBP2: improved version of antibacterial peptide prediction
TL;DR: Among antibacterial peptides, there is preference for certain residues at N and C terminus, which helps to discriminate them from non-antibacterial peptide and their further classification in source and family is studied.
Journal ArticleDOI
Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.
Sneh Lata,Maddalena Marasa,Yifu Li,David Fasel,Emily E. Groopman,Vaidehi Jobanputra,Hila Milo Rasouly,Adele Mitrotti,Rik Westland,Miguel Verbitsky,Jordan G. Nestor,Lindsey M. Slater,Vivette D. D'Agati,Marcin Zaniew,Anna Materna-Kiryluk,Francesca Lugani,Gianluca Caridi,Luca Rampoldi,Aditya Mattoo,Chad A. Newton,Maya K. Rao,Jai Radhakrishnan,Wooin Ahn,Pietro A. Canetta,Andrew S. Bomback,Gerald B. Appel,Corinne Antignac,Glen S. Markowitz,Christine Kim Garcia,Krzysztof Kiryluk,Simone Sanna-Cherchi,Ali G. Gharavi +31 more
TL;DR: Whole-exome sequencing is a genome-wide testing approach that allows selective sequencing of the protein-coding regions of the genome, which are enriched for disease-associated variants and is emerging as a preferred diagnostic tool for hereditary disorders.
Journal ArticleDOI
Next-generation sequencing of endoscopic biopsies identifies ARID1A as a tumor-suppressor gene in Barrett's esophagus.
M. M. Streppel,Sneh Lata,M. Delabastide,Elizabeth A. Montgomery,Jean S. Wang,Marcia I. Canto,Anne Macgregor-Das,Shweta G. Pai,Folkert H.M. Morsink,G. J. A. Offerhaus,E. Antoniou,Anirban Maitra,W. R. McCombie +12 more
TL;DR: ARID1A is identified as a novel tumor-suppressor gene in BE pathogenesis, reiterating the importance of aberrant chromatin in the metaplasia–dysplasia sequence and establishing the feasibility of using mucosal biopsies for NGS, which should enable the comparative analysis of larger ‘progressor’ versus ‘non-progressor' cohorts.