Physics of life reviews Che Jincan, etal High-order interaction modeling of tumor-microenvironment crosstalk for tumor growth 2025
European archives of psychiatry and clinical neuroscience Amin Mutaz, etal Secondary analysis of GenRED data (Genetics of Recurrent Early-Onset major Depression) using MERLIN 2025
Physics reports Feng Li, etal Network modeling and topology of aging 1101, p. 1 - 65 2025
Clinical nutrition open science Gragnoli Claudia, etal Cinnamon treatment shows promise for glycemic control but may cause adverse effects in some people 2025
Journal of ovarian research Wu Rongling, etal The melanocortin receptor genes are linked to and associated with the risk of polycystic ovary syndrome in Italian families 17:1, p. 242 - 5 2024
Aspects of molecular medicine Amin Mutaz, etal Genome-wide linkage and association of novel genes and pathways with type 2 diabetes in Italian families 4 2024
Drug discovery today Che Jincan, etal IdopNetwork as a genomic predictor of drug response, p. 104252 2024
Journal of ovarian research Goparaju Pruthvi, etal Implication of vasopressin receptor genes (AVPR1A and AVPR1B) in the susceptibility to polycystic ovary syndrome 17:1, p. 214 2024
Proceedings of the National Academy of Sciences - PNAS Feng Li, etal Hypernetwork modeling and topology of high-order interactions for complex systems 121:40, p. e2412220121 2024
Aspects of molecular medicine Wu Rongling, etal Linkage and association of rs3110045 and rs28499085 variants in the thyrotropin-releasing hormone receptor (TRHR) gene with the risk of familial type 2 diabetes 3 2024
Journal of ovarian research Postolache Teodor T, etal The melatonin receptor genes are linked and associated with the risk of polycystic ovary syndrome 17:1, p. 17 - 17 2024
Journal of ovarian research Syed Shumail, etal The glucocorticoid receptor gene (NR3C1) is linked to and associated with polycystic ovarian syndrome in Italian families 17:1, p. 13 - 13 2024
European archives of psychiatry and clinical neuroscience Del Bosque-Plata Laura, etal LD block disorder-specific pleiotropic roles of novel CRHR1 in type 2 diabetes and depression disorder comorbidity 2023
Journal of ovarian research Amin Mutaz, etal The prolactin receptor gene (PRLR) is linked and associated with the risk of polycystic ovarian syndrome 16:1, p. 222 - 222 2023
Proceedings of the National Academy of Sciences - PNAS Wu Shuang, etal The metabolomic physics of complex diseases 120:42, p. e2308496120 - e2308496120 2023
European review for medical and pharmacological sciences Amin M, etal Author Correction: Linkage and association of novel DRD2 variants to the comorbidity of type 2 diabetes and depression 27:18, p. 8322 - 8322 2023
Drug discovery today Wang Yu, etal A pleiotropic–epistatic entangelement model of drug response, p. 103790 2023
Journal of ovarian research Amin Mutaz, etal Linkage and association of variants in the dopamine receptor 2 gene (DRD2) with polycystic ovary syndrome 16:1, p. 158 - 158 2023
Genes & diseases Amin Mutaz, etal The role of melatonin receptor 1B gene (MTNR1B) in the susceptibility to depression and type 2 diabetes comorbidity 2023
Drug discovery today Feng Li, etal A personalized pharmaco-epistatic network model of precision medicine 28:7, p. 103608 - 103608 2023
European review for medical and pharmacological sciences Amin M, etal Melatonin receptor 1A (MTNR1A) gene linkage and association to type 2 diabetes in Italian families 27:10, p. 4688 2023
International journal of molecular sciences Amin Mutaz, etal Novel Risk Variants in the Oxytocin Receptor Gene (OXTR) Possibly Linked to and Associated with Familial Type 2 Diabetes 24:7, p. 6282 2023
European review for medical and pharmacological sciences Amin M., etal Oxytocin receptor (OXTR) is a risk gene for polycystic ovarian syndrome 27:6, p. 2634 - 2638 2023
European review for medical and pharmacological sciences Amin M., etal The mineralocorticoid receptor gene (NR3C2) is linked to and associated with polycystic ovarian in Italian families 27:3, p. 942 - 948 2023
Aspects of Molecular Medicine Amin Mutaz, etal Novel linkage and association of the mineralocorticoid receptor gene (NR3C2) with familial type 2 diabetes and depression and their comorbidity 1 2023
Journal of the Endocrine Society Amin Mutaz, etal ODP258 CRHR1 gene shows extensive linkage to major depression and type 2 diabetes in Italian families 6:Supplement_1, p. A339 - A340 2022
International journal of molecular sciences Amin Mutaz, etal Familial Linkage and Association of the NR3C1 Gene with Type 2 Diabetes and Depression Comorbidity 23:19, p. 11951 2022
International journal of molecular sciences Amin Mutaz, etal Comorbidity of Novel CRHR2 Gene Variants in Type 2 Diabetes and Depression 23:17 2022
International journal of molecular sciences Amin Mutaz, etal Implication of Melanocortin Receptor Genes in the Familial Comorbidity of Type 2 Diabetes and Depression 23:15 2022
Journal of Cellular Physiology del Bosque-Plata Laura, etal The broad pathogenetic role of TCF7L2 in human diseases beyond type 2 diabetes 237:1, p. 301 - 312 2022
Diabetes Del Bosque-Plata Laura, etal The Role of TCF7L2 in Type 2 Diabetes 70:6, p. 1220 - 1228 2021
Gut Microbes Jiang Libo, etal A behavioral model for mapping the genetic architecture of gut-microbiota networks 13:1 2021
Cancers Sun Lidan, etal Computational identification of gene networks as a biomarker of neuroblastoma risk 12:8, p. 1 - 17 2020
Journal of Psychiatric Research Akram Faisal, etal Seasonal affective disorder and seasonal changes in weight and sleep duration are inversely associated with plasma adiponectin levels 122, p. 97 - 104 2020
Computational and Structural Biotechnology Journal Sang Mengmeng, etal A rewiring model of intratumoral interaction networks 18, p. 45 - 51 2020
iScience Jiang Libo, etal A Drive to Driven Model of Mapping Intraspecific Interaction Networks 22, p. 109 - 122 2019
Biological psychiatry (1969) Wadhawan Abhishek, etal S144. Obesity is Associated With Anhedonia Only in the Younger Amish Women 85:10, p. S352 - S352 2019
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Postolache Teodor T., etal Co-shared genetics and possible risk gene pathway partially explain the comorbidity of schizophrenia, major depressive disorder, type 2 diabetes, and metabolic syndrome 180:3, p. 186 - 203 2019
Drug Discovery Today Wang Qian, etal A unified mapping framework of multifaceted pharmacodynamic responses to hypertension interventions 24:3, p. 883 - 889 2019
Drug Discovery Today Wei Kun, etal Mapping genes for drug chronotherapy 23:11, p. 1883 - 1888 2018
Gragnoli Claudia, etal Breastfeeding and future maternal health- no causal evidence 2018
Pteridines Ahmad Zaki, etal Sleep onset insomnia, daytime sleepiness and sleep duration in relationship to Toxoplasma gondii IgG seropositivity and serointensity 28:3-4, p. 195 - 204 2017
Pteridines Mohyuddin Hira, etal Seasonality of blood neopterin levels in the Old Order Amish 28:3-4, p. 163 - 176 2017
Frontiers in Public Health Mathai Ashwin Jacob, etal Blood Levels of Monoamine Precursors and Smoking in Patients with Schizophrenia 4 2016
Trends in Genetics Zhu Xuli, etal Integrating Evolutionary Game Theory into Mechanistic Genotype-Phenotype Mapping 32:5, p. 256 - 268 2016
Translational Psychiatry Gragnoli C., etal Dopamine–prolactin pathway potentially contributes to the schizophrenia and type 2 diabetes comorbidity 6:4 2016
Scientific Reports Hao Han, etal T2D and Depression Risk Gene Proteasome Modulator 9 is Linked to Insomnia 5 2015
Journal of Cellular Physiology Gragnoli Claudia, Proteasome modulator 9 gene SNPs, responsible for anti-depressant response, are in linkage with generalized anxiety disorder 229:9, p. 1157 - 1159 2014
Application of Clinical Genetics Gragnoli Claudia, Hypothesis of the neuroendocrine cortisol pathway gene role in the comorbidity of depression, type 2 diabetes, and metabolic syndrome 7, p. 43 - 53 2014
Cardiovascular Diabetology Gragnoli Claudia, Overweight condition and waist circumference and a candidate gene within the 12q24 locus 12:1 2013
Current Medicinal Chemistry Gragnoli C., Proteasome modulator 9 and depression in type 2 diabetes 19:30, p. 5178 - 5180 2012
Journal of Cellular Physiology Oberweis Brandon, etal Potential role of prolactin in antipsychotic-mediated association of schizophrenia and type 2 diabetes 227:8, p. 3001 - 3006 2012
Journal of Cellular Physiology Gragnoli Claudia, Proteasome modulator 9 is linked to microvascular pathology of T2D 227:8, p. 3116 - 3118 2012
Journal of Cellular Physiology Gragnoli Claudia, Depression and type 2 diabetes 227:6, p. 2318 - 2322 2012
Diabetes Research and Clinical Practice Gragnoli Claudia, Proteasome modulator 9 and carpal tunnel syndrome 94:2, p. e47 - e49 2011
Ophthalmic Genetics Gragnoli Claudia, Proteasome modulator 9 gene is linked to diabetic and non-diabetic retinopathy in T2D 32:4, p. 228 - 230 2011
Journal of Diabetes and its Complications Gragnoli Claudia, PSMD9 is linked to type 2 diabetes neuropathy 25:5, p. 329 - 331 2011
Cardiovascular Diabetology Gragnoli Claudia, Proteasome Modulator 9 SNPs are linked to hypertension in type 2 diabetes families 10 2011
Diabetes Research and Clinical Practice Gragnoli Claudia, T2D-nephropathy linkage within 12q24 locus 92:3, p. e73 - e75 2011
Cardiovascular Diabetology Gragnoli Claudia, Hypercholesterolemia and a candidate gene within the 12q24 locus 10 2011
Cardiovascular Diabetology Gragnoli Claudia, Proteasome modulator 9 and macrovascular pathology of T2D 10 2011
Journal of diabetes & metabolism Gragnoli Claudia, Insomnia linked to a T2D Gene 1:S1 2011
Journal of Cellular Physiology Gragnoli Claudia, PSMD9 is linked to MODY3 223:1, p. 1 - 5 2010
Journal of Cellular Physiology Gragnoli Claudia, PSMD9 gene in the NIDDM2 locus is linked to type 2 diabetes in Italians 222:2, p. 265 - 267 2010
Journal of Cellular Physiology Meenakshisundaram Ramachandran, etal CDK4 IVS4-nt40G→A and T2D-associated obesity in Italians rapid communication 221:2, p. 273 - 275 2009
Diabetes Research and Clinical Practice Meenakshisundaram Ramachandran, etal CDK4 IVS4-nt40G → A SNP and type 2 diabetes in Italians 86:2, p. e28 - e30 2009
Obesity Surgery Spanakis Elias, etal Successful medical management of status post-roux-en-y-gastric-bypass hyperinsulinemic hypoglycemia 19:9, p. 1333 - 1334 2009
Obesity Surgery Spanakis Elias, etal Bariatric surgery, safety and type 2 diabetes 19:3, p. 363 - 368 2009
Journal of Experimental and Clinical Cancer Research Meenakshisundaram Ramachandran, etal CDK4 IVS4-nt40 AA genotype and obesity-associated tumors/cancer in Italians - A case-control study 28:1 2009
Journal of Experimental and Clinical Cancer Research Meenakshisundaram Ramachandran, etal CHOP 5'UTR-c.279TC and +nt30CT variants are not associated with overweight condition or with tumors/cancer in Italians-a case-control study 28:1 2009
Journal of Cellular Physiology Spanakis Elias, etal AVPR2 variants and mutations in nephrogenic diabetes insipidus 217:3, p. 605 - 617 2008
Journal of Cellular Physiology Gragnoli Claudia, CHOP T/C and C/T haplotypes contribute to early-onset type 2 diabetes in Italians 217:2, p. 291 - 295 2008
Journal of Cellular Physiology Jonnakuty Catherine, etal What do we know about serotonin? 217:2, p. 301 - 306 2008
Journal of Cellular Physiology Gragnoli Claudia, The CM cell line derived from liver metastasis of malignant human insulinoma is not a valid beta cell model for in vitro studies 216:2, p. 569 - 570 2008
Journal of Cellular Physiology Jonnakuty Catherine, etal Karyotype of the human insulinoma CM cell line - Beta cell model in vitro? 213:3, p. 661 - 662 2007
Journal of Cellular Physiology Gragnoli Claudia, etal Linkage studies for T2D in chop and C/EBPbeta chromosomal regions in Italians 213:2, p. 552 - 555 2007
Journal of Cellular Physiology Gragnoli C., etal PSMD9 gene variants within NIDDM2 may rarely contribute to type 2 diabetes 212:3, p. 568 - 571 2007
Obesity and metabolism Gragnoli Claudia, etal PPAR gamma P12A variant in type 2 diabetes in Italians 3:3, p. 99 - 100 2007
Obesity and metabolism Gragnoli Claudia, Kir6.2 (KCNJ11) E23K variant in Type 2 diabetes in Italians 3:2, p. 97 - 98 2007
Minerva Medica Gragnoli C., etal Meta-analysis of the IPF1 D76N polymorphism in a worldwide type 2 diabetes population 98:3, p. 163 - 166 2007
Obesity and metabolism Milord Edrice, etal Chromosome 10 locus in linkage to type 2 diabetes in Italians 3:1, p. 44 - 47 2007
Minerva Medica Milord E., etal NEUROG3 variants and type 2 diabetes in Italians 97:5, p. 373 - 378 2006
Metabolism: Clinical and Experimental Gragnoli Claudia, etal IPF-1/MODY4 gene missense mutation in an Italian family with type 2 and gestational diabetes 54:8, p. 983 - 988 2005
Metabolism: Clinical and Experimental Gragnoli Claudio, etal Linkage study of the glucagon receptor gene with type 2 diabetes mellitus in Italians 54:6, p. 786 - 787 2005
Metabolism: Clinical and Experimental Gragnoli Claudia, etal Triple genetic variation in the HNF-4α gene is associated with early-onset type 2 diabetes mellitus in a Philippino family 53:8, p. 959 - 963 2004
Diabetologia Gragnoli C., etal Early-onset Type II diabetes mellitus in Italian families due to mutations in the genes encoding hepatic nuclear factor 1α and glucokinase 44:10, p. 1326 - 1329 2001
Human mutation Godart François, etal Identification of seven novel nucleotide variants in the hepatocyte nuclear factor-1α (TCF1) promoter region in MODY patients 15:2, p. 173 - 180 2000
Diabetes Gragnoli Claudia, etal Maturity-onset diabetes of the young due to a mutation in the hepatocyte nuclear factor-4α binding site in the promoter of the hepatocyte nuclear factor-1α gene 46:10, p. 1648 - 1651 1997
Journal of Clinical Investigation Lindner Tom, etal Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4α/MODY1 gene 100:6, p. 1400 - 1405 1997
Diabetes Lindner Tom, etal The 31-cM region of chromosome 11 including the obesity gene tubby and ATP-sensitive potassium channel genes, SUR1 and Kir6.2, Does not contain a major susceptibility locus for NIDDM in 127 non-hispanic white affected sibships 46:7, p. 1227 - 1229 1997
Diabetologia Pozzilli P., etal Double blind trial of nicotinamide in recent-onset IDDM (the IMDIAB III study) 38:7, p. 848 - 852 1995
Journal of Endocrinology Pozzilli P., etal New and old trends for treating organ-specific autoimmune endocrinopathies 145:2, p. 195 - 199 1995
Human Genetics Baroni Marco G., etal Affected sib-pair analysis of the GLUT1 glucose transporter gene locus in non-insulin-dependent diabetes mellitus (NIDDM) 93:6, p. 675 - 680 1994
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Presentations
Amin M and Gragnoli C. Genome-Wide Linkage and Association Study Identifies Novel Genes and Pathways Implicated in Polycystic Ovarian Syndrome. European Society of Human Genetics Hybrid Meeting, Glasgow, Scotland, UK, June10-13, 2023, submitted 2023
del Bosque-Plata L, Amin M, Wu R, Postolache T, and Gragnoli C. Novel TCF7L2 Familial Linkage and Association with Type 2 Diabetes, Depression, and Their Comorbidity. European Society of Human Genetics Hybrid Meeting, Glasgow, Scotland, UK, June10-13, 2023, submitted 2023
Amin M, del Bosque-Plata L, Gonzalez-Ramirez R, Wu R, Postolache TT, Vergare M, Gordon, Ott J, PhD, and Gragnoli C. CRHR1 Gene Shows Extensive Linkage to Major Depression and Type 2 Diabetes in Italian families. Endocrine Society 2022, Atlanta, GA-June 11-14, 2022 2022
Amin M, Ott J, Wu R, Postolache T, Vergare M, Gragnoli C. Comorbidity of CRHR2 Gene Variants in Type 2 Diabetes and Depression. 30th European Congress of Psychiatry (EPA), Budapest, Hungary-April 2-5, 2022 2022
Amin M, Ott J, Wu R, Postolache T, Vergare M, Gragnoli C. Association of CRHR2 Gene Variants with Type 2 Diabetes and Depression. Psych Congress Europe 2022, Barcelona, Spain-February 23-25, 2022 2022
Leadership Speaker Series, CUSOM 2022
Invited speakers for Endocrine Grand Round and Medicine Grand Round to present on R adiofrequency Ablation (RFA) Technique used to cure benign thyroid nodules andm alignant thyroid nodules 2021