Publications by authors named "Claudio Castellan"

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Second-harmonic generation in periodically poled silicon waveguides with lateral p-i-n junctions.
Riccardo Franchi, Claudio Castellan, Mher Ghulinyan, Lorenzo Pavesi

Opt Lett· June 2020

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Second-harmonic generation in periodically poled silicon waveguides with lateral p-i-n junctions: publisher's note.
Riccardo Franchi, Claudio Castellan, Mher Ghulinyan, Lorenzo Pavesi

Opt Lett· June 2020

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On the origin of second harmonic generation in silicon waveguides with silicon nitride cladding.
Claudio Castellan, Alessandro Trenti, Chiara Vecchi, Alessandro Marchesini, Mattia Mancinelli

Sci Rep· January 2019

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Tuning the strain-induced resonance shift in silicon racetrack resonators by their orientation.
Claudio Castellan, Astghik Chalyan, Mattia Mancinelli, Pierre Guilleme, Massimo Borghi

Opt Express· February 2018

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Single-nucleotide polymorphism array-based characterization of ring chromosome 18.
Ana Spreiz, Roberta S Guilherme, Claudio Castellan, Andrew Green, Olaf Rittinger

J Pediatr· October 2013

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[Genomics in medicine: challenges and perspectives for the nursing care].
Maria Grazia Romanelli, Laura Pressi, Maria Regele, Claudio Castellan

Assist Inferm Ric· November 2010

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Interesting suggestions about Yq deletions.
Francesco Benedicenti, Claudio Castellan

Fertil Steril· January 2009

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Characterization of interstitial Xp duplications in two families by tiling path array CGH.
Andreas Tzschach, Wei Chen, Fikret Erdogan, Adelheid Hoeller, Hans-Hilger Ropers, Claudio Castellan

Am J Med Genet A· January 2008

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Infantile encephalopathy and defective mitochondrial DNA translation in patients with mutations of mitochondrial elongation factors EFG1 and EFTu.
Lucia Valente, Valeria Tiranti, Rene Massimiliano Marsano, Edoardo Malfatti, Erika Fernandez-Vizarra, Claudio Castellan

Am J Hum Genet· January 2007

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CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.
Susanne Kohl, Balazs Varsanyi, Gesine Abadin Antunes, Britta Baumann, Carel B Hoyng, Claudio Castellan

Eur J Hum Genet· March 2005

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Utilization of genetic counseling by parents of a child or fetus with congenital malformation in North-East Italy.
Isabella Mammi, Rosaria Teresa Basile, Silvano Bellato, Serena Belli, Francesco Benedicenti, Claudio Castellan

Am J Med Genet A· September 2003

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Neurofibromatosis type 1 (NF1): Identification of eight unreported mutations in NF1 gene in Italian patients [corrected].
Paola Origone, Carlo Bellini, Debora Sambarino, Barbara Banelli, Guido Morcaldi, Claudio Castellan

Hum Mutat· August 2003

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Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet-Biedl patients with two mutations at a second BBS locus.
Jose L Badano, Jun Chul Kim, Bethan E Hoskins, Richard Alan Lewis, Stephen J Ansley, Claudio Castellan

Hum Mol Genet· July 2003

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Mutations spectrum of GNE in hereditary inclusion body myopathy sparing the quadriceps.
Iris Eisenberg, Gil Grabov-Nardini, Hagit Hochner, Mira Korner, Menachem Sadeh, Claudio Castellan

Hum Mutat· January 2003

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Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene.
Tamio Suzuki, Wei Li, Qing Zhang, Amna Karim, Edward K Novak, Claudio Castellan

Nat Genet· March 2002

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