1 - 25 of
35
results
for author:"Colombo C."
in Literature Citations
| Genetic modifiers of liver disease in cystic fibrosis. Bartlett J.R., Friedman K.J., Ling S.C., Pace R.G., Bell S.C., Bourke B., Castaldo G., Castellani C., Cipolli M., Colombo C. et al. JAMA 302:1076-1083(2009) · Mapped (24) |
| 5-HT2A gene variants influence specific and different aspects of antidepressant response in Japanese and Italian mood disorder patients. Kato M., Zanardi R., Rossini D., De Ronchi D., Okugawa G., Kinoshita T., Colombo C., Serretti A. Psychiatry Res 167:97-105(2009) · Mapped (3) |
| Expression of apoptosis-related proteins and of mRNA for dopaminergic receptors in peripheral blood mononuclear cells from patients with Alzheimer disease. Cosentino M., Colombo C., Mauri M., Ferrari M., Corbetta S., Marino F., Bono G., Lecchini S. Alzheimer Dis Assoc Disord 23:88-90(2009) · Mapped (20) |
| The catechol-O-methyltransferase Val(108/158)Met polymorphism affects antidepressant response to paroxetine in a naturalistic setting. Benedetti F., Colombo C., Pirovano A., Marino E., Smeraldi E. Psychopharmacology (Berl.) 203:155-160(2009) · Mapped (8) |
| Interaction between SERTPR and stressful life events on response to antidepressant treatment. Mandelli L., Marino E., Pirovano A., Calati R., Zanardi R., Colombo C., Serretti A. Eur Neuropsychopharmacol 19:64-67(2009) · Mapped (4) |
| Serotonin 5-HT2A receptor gene variants influence antidepressant response to repeated total sleep deprivation in bipolar depression. Benedetti F., Barbini B., Bernasconi A., Fulgosi M.C., Colombo C., Dallaspezia S., Gavinelli C., Marino E., Pirovano A., Radaelli D. et al. Prog. Neuropsychopharmacol. Biol. Psychiatry 32:1863-1866(2008) · Mapped (3) |
| A length polymorphism in the circadian clock gene Per3 influences age at onset of bipolar disorder. Benedetti F., Dallaspezia S., Colombo C., Pirovano A., Marino E., Smeraldi E. Neurosci. Lett. 445:184-187(2008) · Mapped (7) |
| Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus. Colombo C., Porzio O., Liu M., Massa O., Vasta M., Salardi S., Beccaria L., Monciotti C., Toni S., Pedersen O. et al. J. Clin. Invest. 118:2148-2156(2008) · Mapped (1) |
| Molecular and clinical features associated with CFTR gene rearrangements in Italian population: identification of a new duplication and recurrent deletions. Paracchini V., Seia M., Coviello D., Porcaro L., Costantino L., Capasso P., Degiorgio D., Padoan R., Corbetta C., Claut L. et al. Clin. Genet. 73:346-352(2008) · Mapped (46) |
| The G53D mutation in Kir6.2 (KCNJ11) is associated with neonatal diabetes and motor dysfunction in adulthood that is improved with sulfonylurea therapy. Koster J.C., Cadario F., Peruzzi C., Colombo C., Nichols C.G., Barbetti F. J. Clin. Endocrinol. Metab. 93:1054-1061(2008) · Mapped (4) |
| Association between GSK-3beta -50T/C polymorphism and personality and psychotic symptoms in mood disorders. Serretti A., Benedetti F., Mandelli L., Calati R., Caneva B., Lorenzi C., Fontana V., Colombo C., Smeraldi E. Psychiatry Res 158:132-140(2008) · Mapped (3) |
| Missense mutations in the TGM2 gene encoding transglutaminase 2 are found in patients with early-onset type 2 diabetes. Porzio O., Massa O., Cunsolo V., Colombo C., Malaponti M., Bertuzzi F., Hansen T., Johansen A., Pedersen O., Meschi F. et al. |
| Molecular characterization and structural implications of 25 new ABCB4 mutations in progressive familial intrahepatic cholestasis type 3 (PFIC3). Degiorgio D., Colombo C., Seia M., Porcaro L., Costantino L., Zazzeron L., Bordo D., Coviello D.A. Eur. J. Hum. Genet. 15:1230-1238(2007) · Mapped (8) |
| 5-HT2A SNPs and the Temperament and Character Inventory. Serretti A., Calati R., Giegling I., Hartmann A.M., Moller H.J., Colombo C., Rujescu D. Prog. Neuropsychopharmacol. Biol. Psychiatry 31:1275-1281(2007) · Mapped (3) |
| Clock genes beyond the clock: CLOCK genotype biases neural correlates of moral valence decision in depressed patients. Benedetti F., Radaelli D., Bernasconi A., Dallaspezia S., Falini A., Scotti G., Lorenzi C., Colombo C., Smeraldi E. Genes Brain Behav. 7:20-25(2008) · Mapped (7) |
| Synaptophysin I selectively specifies the exocytic pathway of synaptobrevin 2/VAMP2. Bonanomi D., Rusconi L., Colombo C.A., Benfenati F., Valtorta F. Biochem. J. 404:525-534(2007) · Mapped (6) |
| An ATP-binding mutation (G334D) in KCNJ11 is associated with a sulfonylurea-insensitive form of developmental delay, epilepsy, and neonatal diabetes. Masia R., Koster J.C., Tumini S., Chiarelli F., Colombo C., Nichols C.G., Barbetti F. Diabetes 56:328-336(2007) · Mapped (4) |
| Actimetric evidence that CLOCK 3111 T/C SNP influences sleep and activity patterns in patients affected by bipolar depression. Benedetti F., Dallaspezia S., Fulgosi M.C., Lorenzi C., Serretti A., Barbini B., Colombo C., Smeraldi E. Am. J. Med. Genet. B Neuropsychiatr. Genet. 144B:631-635(2007) · Mapped (7) |
| Serotonin transporter gene influences the time course of improvement of "core" depressive and somatic anxiety symptoms during treatment with SSRIs for recurrent mood disorders. Serretti A., Mandelli L., Lorenzi C., Pirovano A., Olgiati P., Colombo C., Smeraldi E. Psychiatry Res 149:185-193(2007) · Mapped (4) |
| Interaction between serotonin transporter gene, catechol-O-methyltransferase gene and stressful life events in mood disorders. Mandelli L., Serretti A., Marino E., Pirovano A., Calati R., Colombo C. Int. J. Neuropsychopharmacol. 10:437-447(2007) · Mapped (75) |
| Insomnia improvement during antidepressant treatment and CLOCK gene polymorphism. Serretti A., Cusin C., Benedetti F., Mandelli L., Pirovano A., Zanardi R., Colombo C., Smeraldi E. Am. J. Med. Genet. B Neuropsychiatr. Genet. 137B:36-39(2005) · Mapped (7) |
| Fcgamma receptor IIA genotype and susceptibility to P. aeruginosa infection in patients with cystic fibrosis. De Rose V., Arduino C., Cappello N., Piana R., Salmin P., Bardessono M., Goia M., Padoan R., Bignamini E., Costantini D. et al. Eur. J. Hum. Genet. 13:96-101(2005) · Mapped (49) |
| A glycogen synthase kinase 3-beta promoter gene single nucleotide polymorphism is associated with age at onset and response to total sleep deprivation in bipolar depression. Benedetti F., Serretti A., Colombo C., Lorenzi C., Tubazio V., Smeraldi E. Neurosci. Lett. 368:123-126(2004) · Mapped (3) |
| Genetic background (C57BL/6J versus FVB/N) strongly influences the severity of diabetes and insulin resistance in ob/ob mice. Haluzik M., Colombo C., Gavrilova O., Chua S., Wolf N., Chen M., Stannard B., Dietz K.R., Le Roith D., Reitman M.L. Endocrinology 145:3258-3264(2004) · Mapped (2) |
| A single nucleotide polymorphism in glycogen synthase kinase 3-beta promoter gene influences onset of illness in patients affected by bipolar disorder. Benedetti F., Bernasconi A., Lorenzi C., Pontiggia A., Serretti A., Colombo C., Smeraldi E. Neurosci. Lett. 355:37-40(2004) · Mapped (3) |
