Biography
Dr. K. Gus Kousoulas received his BS in Physics from Fairleigh Dickinson University in Teaneck, NJ, and his MS and PhD degrees from Pennsylvania State University in Biophysics and Molecular Cell Biology, respectively. Dr. K. Gus Kousoulas received postdoctoral training at the University of Chicago working in Dr. Bernard Roizman’s laboratory and at the University of California at San Francisco with Dr. Lenore Pereira, where later he was promoted to Research Assistant Professor. Dr. K. Gus Kousoulas joined Louisiana State University in Baton Rouge, LA in 1988 and became full professor in 1994. Dr. K. Gus Kousoulas is currently Professor of Virology at the LSU School of Veterinary Medicine with adjunct appointments at the Department of Biological Sciences, College of Basic Sciences, the Department of Microbiology and Immunology at the LSU Health Sciences Center in New Orleans, and the LSU Health Sciences Center’s Gene Therapy Program and the Stanley S. Scott Cancer Center in New Orleans. He is also an affiliate member of the Tulane National Primate Research Center located in Covington, LA. Dr. Kousoulas has been independently funded by NIH with R01 grants since 1990 working on the molecular biology of herpes simplex virus. Dr. K. Gus Kousoulas is the Principal Investigator of the LSU-Tulane Center for Experimental Infectious Diseases, which is funded by the NIH:NCRR: COBRE mechanism and a mentor of a junior investigator in the LSU Health Sciences Center School of Dentistry COBRE (PI: Paul Fidel). Dr. Kousoulas is a member of the Steering Committee of the LSU Baton Rouge-led NCRR: INBRE program and leads the molecular and cellular biology core of the INBRE. Dr. Kousoulas has served on a number of NIH panels including the NCRR Comparative Medicine Panel and other NIH panels and site visit teams of National Primate Research Centers.
Research Interest
Dr. K. Gus Kousoulas primary research interests are focused on the molecular biology and pathogenesis of herpes simplex viruses (HSV) and human herpesvirus 8 (HHV-8) or Kaposi’s Sarcoma-Associated Herpesvirus (KSHV). Specifically, he seeks to define the molecular mechanisms that control attachment and penetration of these viruses into susceptible cells (including cells of neuronal origin for HSV), their ability to replicate and spread from cell to cell, and the role of membrane fusion events in intracellular virion transport and egress. His experimental approach utilizes advanced molecular biology, molecular genetics and cell biology. Briefly, mutant herpesviruses deficient in a particular function are isolated through generalized mutagenesis, site-specific mutagenesis of viral genomes cloned into bacterial artificial chromosomes (BAC). These engineered viruses are studied to learn about the role of specific virus encoded proteins in host cell attachment, penetration, virus induced cell fusion virion assembly and egress. To analyze the role of specific viral genes in virus penetration and virus-induced cell fusion these genes are expressed in transient, eukaryotic expression systems and the expressed proteins are detected using specific monoclonal antibodies produced in my laboratory. In addition, monoclonal and monospecific sera against viral proteins are utilized to locate their target proteins in infected cells using confocal and immunoelectron microscopy and to analyze their structure and function. A major finding from our studies has implicated multiple protein-protein interactions among viral membrane proteins of both HSV-1 and KSHV in regulation of virus-induced membrane fusion phenomena. Similarly, multiple interactions among membrane proteins and tegument proteins have been found to regulate cytoplasmic virion envelopment. A second major recent interest of his laboratory is the use of viral vectors for gene and ancer therapy and vaccine purposes. Currently funded projects include the generation of oncolytic recombinant herpes simplex virus vectors to combat breast cancer (Louisiana Board of Regents and Louisiana Gene Therapy and Cancer Consortia). These viruses are tested in zenograft mouse models using human breast cancer cells. A significant effort is focused on the production of vaccines for West Nile virus, herpes B virus and Simian Retrovirus using vesicular stomatitis virus (VSV) and adenovirus-based vectors. This work is carried out in collaboration with the Tulane National Research Primate Center (Dr. Preston Marx). A fourth research interest of Dr. K. Gus Kousoulas laboratory is the molecular biology and pathogenesis of human and bovine coronaviruses. Dr. K. Gus Kousoulas has derived and compared the entire genomic nucleotide sequence of several respiratory and enteric bovine coronaviruses and identified specific nucleotide changes, which may be associated with virus tropism. Dr. K. Gus Kousoulas is particularly interested in the structure and function of the viral spike glycoproteins encoded by the SARS coronavirus and respiratory bovine coronaviruses, which are known to promote virus entry into susceptible cells and virus-induced membrane fusion phenomena.
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 Gottfried Baier
 
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 F I D Konotey-Ahulu
 
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 Katherine S Ancell and Deborah A Bruns
 
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 Filiptsova OV and Atramentova LA
 
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 DOI: 10.4172/2327-5790.1000149
 Iwanicka-Pronicka K, Pajdowska M, Dariusz Rokicki, Piekutowska-Abramczuk D, Kozlowski D,Wisniewska-Ligier D, Ksiazyk JB, Krajewska-Walasek M, Wolf B and Pronicka E
 
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 Farid Ahmed
 
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 Mich González
 
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 William J. Rowe
 
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 Nasser Khan
 
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 Dalton Smith
 
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 RAUSCHER ALEXANDER
 
-  Young Scientist Awards at Genome Editing 2020 for the best researches in Genome Editing and Gene TherapyYoung Research Forum: J Genet Disor Genet Rep
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 William J. Rowe
 
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 Alireza Heidari
 
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 Dan Hauzenberger*
 
-  Molecular Genetic Testing for Carrier - Prenatal Diagnosis and Computational Analysis of Oculocutaneous Albinism Type 1Research Article: J Genet Disor Genet Rep 2014, 3:2
 DOI: 10.4172/2327-5790.1000117
 Kathirvel Renugadevi, John Asnet Mary, Vijayalakshmi Perumalsamy, Suresh Seshadri, Sujatha Jagadeesh, Beena Suresh, Sheela Nampoothiri, Rajaiah Shenbagarathai, Sankaran Krishnaswamy and Periasamy Sundaresan
 
-  Molecular characterization of Galactosemia in Iran: identification of Eleven mutations.Research Article: J Genet Disor Genet Rep
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 Mehrnoosh Moody
 
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 Cipta Mahendra
 
-  Endometrial Disease in AdultsOpinion Article: J Genet Disor Genet Rep
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 Thomas Aldy
 
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 David Farooq
 
-  Drawn out Pregnancy is Related with an Increment in Perinatal Horribleness during Child BirthOpinion Article: J Genet Disor Genet Rep
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 Laura Lewis
 
-  How Menopause Causes Health Issues in Women after PregnencyCommentary: J Genet Disor Genet Rep
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 Lambrinoudaki Caty
 
-  Thyroid Issues can be Difficult to Analyze in PregnancyPerspective: J Genet Disor Genet Rep
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 Chan Li
 
-  Chromosomal Abnormalities: Causes and Effects on DevelopmentPerspective:
 DOI:
 Mustafa Gokhan Ertosun
 
-  A Rare Familial Paracentric Inversion in the Long Arm of Chromosome 8: Case Report and Review of the LiteratureResearch Article: J Genet Disor Genet Rep, 6:2
 DOI: 10.4172/2327-5790.1000152
 Kouvidi E, Tsarouha H, Zachaki S, Mitrakos A, Sfakianoudis K, Kanavakis E, Mavrou A
 
-  Homozygous Point Mutation in a Patient with Spinal Muscular Atrophy Type 1Case Report: J Genet Disor Genet Rep 2016, 5:3
 DOI: 10.4172/2327-5790.1000137
 Isa Abdi Rad, Ali Vahabi and Ahad Ghazavi
 
-  Investigation of the Origin of Common LDLR Mutation Alleles in New Zealand Familial Hypercholesterolemia PatientsResearch Article: J Genet Disor Genet Rep, 7:1
 DOI: 10.4172/2327-5790.1000167
 Laurie AD, Spain RJ, Reid N and George PM
 
-  Challenging Reproductive Genetic Counseling in Families at High Risk for Rare Genetic Syndromes â A Case Report with Possible Denys-Drash SyndromeCase Report: J Genet Disor Genet Rep, 7:2
 DOI: 10.4172/2327-5790.1000172
 Hachmeriyan M, Andonova S, Levkova M, Stoyanova M, Kalchev K, Vasilev P, Miteva V, Tsvetkova M, Bradinova I and Angelova L
 
-  Severe Expressive-Language Delay and Congenital Malformations in a Boy with Microduplication 7q11.23 Diagnosed by Molecular Cytogenetic AnalysisResearch Article: J Genet Disor Genet Rep 2016, 5:1
 DOI: 10.4172/2327-5790.1000127
 Inesse Ben-Abdallah-Bouhjar, Amal Al Hashem, Samia Sobki, Brahim Tabarki, Yasser Hassen Babair and Hatem Elghezal
 
-  Mutational Analysis in Gaucher Disease: Implications in Genetic Counseling and Management.Research Article: J Genet Disor Genet Rep 2016, 5:2
 DOI: 10.4172/2327-5790.1000132
 Inusha Panigrahi, Jaswinder Kalra, Prasoon Goyad, Preeti Khetarpal and Anjana Munshi
 
-  Treatment with Agalsidase Alfa during Pregnancy in a Heterozygous Female with Fabry DiseaseCase Report: J Genet Disor Genet Rep, 5:4
 DOI: 10.4172/2327-5790.1000143
 Antonio Pisani, Giuseppe Bifulco, Attilio Di Spiezio Sardo and Eleonora Riccio
 
-  A Rett Syndrome Case with Mutation in MECP2 and Deletion of 16p11.2Case Report: J Genet Disor Genet Rep, 6:3
 DOI: 10.4172/2327-5790.1000158
 Bossolani-Martins AL, Moreira DP, Lourenço NCV, Magalhaes ML, Ribeiro CM, Griesi-Oliveira K and Fett-Conte AC
 
-  Intergenerational De Novo Spinocerebellar Ataxia 7 CAG Enlargement in a Moroccan Family Detected by Triplet Primed PCRResearch Article: J Genet Disor Genet Rep, 6:4
 DOI: 10.4172/2327-5790.1000163
 Martínez-Laso J, Giménez-Pardo A Jimenez E, Gallego J, Cervera I, Ayuso C, Lorda I and Trujillo-Tiebas MJ
 
-  Evidence that lithium Inhibits Export of N-Acetyl-L-Aspartate from Neurons: A Retrospective Study of Canavan Disease and Bipolar Disorder PatientsResearch Article: J Genet Disor Genet Rep 2014, 3:1
 DOI: 10.4172/2327-5790.1000110
 Morris H Baslow and David N Guilfoyle
 
-  Hereditary Thrombocytosis in 3 Kuwaiti Siblings with Homozygous MPL Pro106Leu Mutation and Abnormal Platelet AggregationCase Report: J Genet Disor Genet Rep 2013, 2:2
 DOI: 10.4172/2327-5790.1000105
 Preethi Reddy Marri, Salman Kirmani and Vilmarie Rodriguez
 
-  Whole Exome Sequencing found a Novel Truncating Mutation within CNTNAP2 Gene in an Iranian Patient with Mental RetardationCase Report: J Genet Disor Genet Rep, 7:3
 DOI: 10.4172/2327-5790.1000177
 Mehrnoosh Shokoohi, Mohammadreza Hajjari, Javad Mohammadiasl J and Maryam Tahmasebi Birgani MT
 
-  Inherited Unbalanced Chromosome from Parent with Balanced Translocation: A Case Report and Review of LiteratureCase Report: J Genet Disor Genet Rep 2016, 5:3
 DOI: 10.4172/2327-5790.1000138
 Kumari P, Mishra VV and Tewari S
 
-  TLR4 and NOD2/CARD15 Polymorphisms and Their Association with Dietary Factors in Colorectal CancerResearch Article: J Genet Disor Genet Rep, 7:1
 DOI: 10.4172/2327-5790.1000168
 Omrane I, Baroudi O, Medimegh I, Ayari H, Kourda N, Mezlini A and Benammar-Elgaaied A
 
-  Phenylketonuria and GeneticsReview Article: J Genet Disor Genet Rep, 7:2
 DOI: 10.4172/2327-5790.1000173
 Ittan SP
 
-  Screening of Genetic Mutations in GBA1, GIGYF2 and VPS35 in Parkinson Disease Patients from IndiaResearch Article: J Genet Disor Genet Rep, 5:4
 DOI: 10.4172/2327-5790.1000144
 Tamali Halder, Janak Raj, Sharad Pandey, Ajay Kumar, Sagar Kawale, Sandeep Chaudhary, Vivek Sharma, Deepika Joshi and Parimal Das
 
-  The Genomic Novel and Priority Mapping Tool: Using Empathic Design to Develop Innovative Patient-Centered Decision-Making Tools for the Genomic Testing ExperienceResearch Article: J Genet Disor Genet Rep 2016, 5:1
 DOI: 10.4172/2327-5790.1000128
 Kiley J Johnson, Kimberly A Schahl, Pamela S Sinicrope, Tammy M McAllister, Jennifer B McCormick, Leslie E Ruckman, Mekayla I Beaver and Noralane M Lindor
 
-  Comprehensive Review of Rare Hereditary Autoinflammatory DisordersReview Article: J Genet Disor Genet Rep 2013, 2:2
 DOI: 10.4172/2327-5790.1000106
 Nobuo Kanazawa
 
-  The Interpretation of Genetic Data - Considering the Effect of Changes to Gene Conformation - If the Facts Donât Support the Theory, Change the Theory â How Does This Contribute to Understanding Diabetes?Commentary: J Genet Disor Genet Rep, 6:4
 DOI: 10.4172/2327-5790.1000164
 Ewing GW
 
-  Cerebellar Hypoplasıa as a Manıfestatıon of 6q25 Deletıon in a Preterm NewbornCase Report: J Genet Disor Genet Rep, 7:3
 DOI: 10.4172/2327-5790.1000178
 Demırel G, Vatansever B, Karavar H, Gundogdu S, Ertan G and Tastekın A
 
-  Resistance of Culex pipiens (Diptera: Culicidae) to Chlorpyrifos Insecticide in Central TunisiaResearch Article: J Genet Disor Genet Rep, 6:3
 DOI: 10.4172/2327-5790.1000159
 Jaber Daaboub, Ahmed Tabbabi, Raja Ben Cheikh, Ali Lamari, Ibtissem Ben Jha and Hassen Ben Cheikh
 
-  Growth Abnormalities Resulting in Short Stature in Genetic SyndromesReview Article: J Genet Disor Genet Rep 2014, 3:1
 DOI: 10.4172/2327-5790.1000111
 Lena Dain1 and Stavit A Shalev
 
-  Pallister-Killian Syndrome: Undetected by Percutaneous Umbilical Blood Karyotyping and Neonatal Blood Microarray Comparative Genomic HybridizationResearch Article: J Genet Disor Genet Rep, 6:2
 DOI: 10.4172/2327-5790.1000153
 Huang MH, Yang IF, Lee C, Chang JS, Wang HC, Tou WS, Ling FC, Lai HL, Tsai LP and Ho SP
 
-  A Case of Wolf-Hirschhorn Syndrome and Familial Mediterranean FeverCase Report: J Genet Disor Genet Rep 2016, 5:2
 DOI: 10.4172/2327-5790.1000133
 Kazuaki Matsumoto* and Masayasu Ohta
 
-  A case of Tuberous Sclerosis Complex Masquerading as Birt-Hogg-Dubé SyndromeCase Report: J Genet Disor Genet Rep, 7:1
 DOI: 10.4172/2327-5790.1000169
 Kong YL, Oon HH, Choudhury Y, Tan MH and Ng SK
 
-  A Rare Case of Isodicentric Xq28 that Causes Mental Retardation: Molecular Characterization and ReviewResearch Article: J Genet Disor Genet Rep, 6:2
 DOI: 10.4172/2327-5790.1000154
 Gonzalez C, Gutierrez M, Ruiz ML, Huete B, Gonzalez S, Gallego J and Cava F
 
-  Are Antimullerian Hormone and its Receptor Genes Associated with Low Ovarian Response?Research Article: J Genet Disor Genet Rep 2014, 3:1
 DOI: 10.4172/2327-5790.1000112
 Chelsi Goodman, Hosam Zaki, Larry Fischel, Hisham Greiss and Carolyn Coulam
 
-  Evaluation of Genomic Evidence for Oxidative Stress in Experimental Radiation NephropathyResearch Article: J Genet Disor Genet Rep 2013, 2:1
 DOI: 10.4172/2327-5790.1000101
 Eric P Cohen, Marek Lenarczyk, Brian L Fish, Shuang Jia, Martin J Hessner and John E Moulder
 
-  Left Ventricular Noncompaction in Noonan SyndromeCase Report: J Genet Disor Genet Rep 2016, 5:2
 DOI: 10.4172/2327-5790.1000134
 Robert B Hinton, Paula Goldenberg, Richard C Godby, Ashley Parrott, Amy G Shikany, Benjamin J Landis, Jeanne F James, Erin M Miller, Stephanie M Ware
 
-  Hearing in Williams Syndrome: From Input to ProcessingReview Article: J Genet Disor Genet Rep, 7:2
 DOI: 10.4172/2327-5790.1000174
 Fagundes Silva LA, Kim CA and Matas CG
 
-  Anti-Ige (Omalizumab) Improved Trombotic Emboli by Elevating Activated Protein C, Protein S, and Antithrombin III in a Case of Prothrombin G20210A Mutation: Long Term Follow-UpLetter to Editor: J Genet Disor Genet Rep 2016, 5:1
 DOI: 10.4172/2327-5790.1000129
 Arzu Didem Yalcin and Betul Celik
 
-  Congenital Cerebral Ischemic Lesions in Monochorionic TwinsCase Report: J Genet Disor Genet Rep 2013, 2:2
 DOI: 10.4172/2327-5790.1000107
 Olajide Dolapo and Ravi Kudumula
 
-  Rare Unusual Coincidence of LeriâWeill Dyschondrosteosis Resulting from a Downstream Enhancer Deletion of SHOX Gene and Neurofibromatosis Type 1Case Report: J Genet Disor Genet Rep, 6:4
 DOI: 10.4172/2327-5790.1000165
 Peleg A, Adir V, Larom-Khan G, Harari Shaham A and Sagi-Dain L
 
-  Clinical and Molecular Assessment in a Female with Fragile X Syndrome and Tuberous SclerosisResearch Article: J Genet Disor Genet Rep 2016, 5:3
 DOI: 10.4172/2327-5790.1000139
 Carolyn M Yrigollen, Laura Pacini, Veronica Nobile, Reymundo Lozano, Randi J Hagerman, Claudia Bagni and Flora Tassone
 
-  Smith-Magenis Syndrome Treated with Ramelteon and Amphetamine-dextroamphetamine: Case Report and Review of the LiteratureCase Report: J Genet Disor Genet Rep, 5:4
 DOI: 10.4172/2327-5790.1000145
 Baek WS, Elsea SH
 
-  Non-Viral Vectors for Cystic Fibrosis Therapy: Recent AdvancesReview Article: J Genet Disor Genet Rep, 7:3
 DOI: 10.4172/2327-5790.1000179
 Faisal Qaisar, Anum Habib, Noor Muhammad and Zia ur Rehman
 
-  A New Case of Microdeletion 5q11.2 with Segmental 5q Isodisomy and Review of the LiteratureCase Report: J Genet Disor Genet Rep, 6:3
 DOI: 10.4172/2327-5790.1000160
 Pecile V, Devescovi R, Cappellani S, Faletra F and Lenzini E
 
-  Long-Term Follow-Up of a Patient with Sitosterolemia and Hemolytic Anemia with Excellent Response to EzetimibeCase Report: J Genet Disor Genet Rep 2013, 2:1
 DOI: 10.4172/2327-5790.1000102
 Alfonso Quint?s-Cardama and John J. McCarthy
 
-  Same Mutation in Two Patients with Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome) Coming from Different Municipalities in the Department of Cauca, Southwestern ColombiaResearch Article: J Genet Disor Genet Rep, 5:4
 DOI: 10.4172/2327-5790.1000146
 Acosta MA, Lago RM, Barros F and Carracedo AM
 
-  Lipoprotein Glomerulopathy: Molecular Characterization of Three Italian Patients and Literature SurveyResearch Article: J Genet Disor Genet Rep 2014, 3:1
 DOI: 10.4172/2327-5790.1000113
 Antonio Pasquariello, Livia Pisciotta, Tiziana Sampietro, Giovanna Pasquariello, Pellegrino Masiello, Matilde Masini, Francesco Sbrana, Mariarita Puntoni, Roberto Miccoli, Sebastiano Calandra and Stefano Bertolini
 
-  Association of HLA Typing with Nicotine Dependence by Extraction of Salivary DNA among Indian PopulationResearch Article: J Genet Disor Genet Rep, 7:1
 DOI: 10.4172/2327-5790.1000170
 Purohit A, Purohit BM, Mani A and Bhambal A
 
-  Patterns of Utilization of Genetic Services Following the Initiation of Community based Primary Care Carrier Screening in a Traditional Muslim CommunityResearch Article: J Genet Disor Genet Rep, 7:2
 DOI: 10.4172/2327-5790.1000175
 Abu-Rabia R, Abo Rabia A, Birk O and Elana Shoham-Vardi
 
-  Spectrum of CFTR Mutations in the Algerian Population: Molecular and Computational AnalysisResearch Article: J Genet Disor Genet Rep 2016, 5:1
 DOI: 10.4172/2327-5790.1000130
 Fatima Zohra Sediki, Abdelkarim Radoui, Abdallah Boudjema, Meriem Abdi, Faouzia Zemani-Fodil, Nadhira Saidi-Mehtar and Faiza Cabet
 
-  The Prevalence of Three Common MEFV Gene Mutations in West Bank Population among Students of Najah National University, PalestineResearch Article: J Genet Disor Genet Rep, 6:4
 DOI: 10.4172/2327-5790.1000166
 Tanbour RG, Sawafta TS and Basha WS
 
-  Phenylketonuria (PKU) - What Next? Mini-ReviewReview Article: J Genet Disor Genet Rep 2013, 2:2
 DOI: 10.4172/2327-5790.1000108
 WB Hanley
 
-  Cerebrovascular and Brain Abnormalities in Autosomal- Dominant Polycystic Kidney Disease: Role of 3d Time-of-Flight Magnetic Resonance AngiographyResearch Article: J Genet Disor Genet Rep 2016, 5:3
 DOI: 10.4172/2327-5790.1000140
 Carmela Russo, Ferdinando Caranci, Massimo Imbriaco, Manuela Napoli, Antonio Pisani, Eleonora Riccio, Michele Santangelo, Sirio Cocozza, Enrico Tedeschi, Francesco Briganti and Arturo Brunetti
 
-  Atypical Hypotonia-Cystinuria a New Case: Genotype-Phenotype, DescriptionCase Report: J Genet Disor Genet Rep, 7:3
 DOI: 10.4172/2327-5790.1000180
 Preka Evgenia, Ariane Paoloni-Giacobino, Frédérique Sloan-Béna, Paloma Parvex and Alexandra Wilhelm-Bals
 
-  Pirimiphos-methyl Resistance in Culex pipiens (Diptera: Culicidae) in Southern TunisiaResearch Article: J Genet Disor Genet Rep, 6:2
 DOI: 10.4172/2327-5790.1000155
 Tabbabi Ahmed, Daaboub Jaber, Laamari Ali, Ben Cheikh Raja and Ben Cheikh Hassen
 
-  Variation of Abnormal Hemoglobins Concentrated in Durg, Chhattisgarh: A Brief Note Based on Cross-Sectional StudyCase Report: J Genet Disor Genet Rep 2016, 5:2
 DOI: 10.4172/2327-5790.1000135
 Devendra Lingojwar, Pramod Gupta, Savita Bhutoria, Sarita Lingojwar, Nikhil Mishra, Anil Kumar
 
-  Chlorpyrifos Resistance Characteristics of Culex pipiens (Diptera: Culicidae) from Northern TunisiaResearch Article: J Genet Disor Genet Rep, 6:3
 DOI: 10.4172/2327-5790.1000161
 Jaber Daaboub, Ahmed Tabbabi, Ali Lamari, Mohamed Feriani, Chokri Boubaker and Hassen Ben Cheikh
 
-  Erring on the Side of Life: Children with Rare Trisomy Conditions, Medical Interventions and Quality of LifeReview Article: J Genet Disor Genet Rep 2013, 2:1
 DOI: 10.4172/2327-5790.1000103
 Deborah A. Bruns
 
-  Involvement of TLR4 Polymorphisms on Colorectal Cancer TreatmentResearch Article: J Genet Disor Genet Rep, 7:1
 DOI: 10.4172/2327-5790.1000171
 Omrane I, Baroudi O, Medimegh I, Ayari H, Kourda N, Mezlini A, Bougatef K and Benammar-Elgaaied A
 
-  Advances of Programmed Death-1/Programmed Death-1 Ligand Signal Pathway and its Blockers in Nasopharyngeal CarcinomaReview Article: J Genet Disor Genet Rep, 7:2
 DOI: 10.4172/2327-5790.1000176
 Zhou Q, Assani G, Ling H, Xiong Y and Zhou Y
 
-  Telomeres in Cancer: Length, Positioning and EpigeneticsReview Article: J Genet Disor Genet Rep 2016, 5:1
 DOI: 10.4172/2327-5790.1000131
 Patel TN, Sulekha R Nair, Lekshmi Mohan, Fahmina Y, Ashwini, Devi S and VA Saimadhukiran Dabbiru
 
-  Expression of TCTP-Related GenesResearch Article: J Genet Disor Genet Rep, 6:2
 DOI: 10.4172/2327-5790.1000156
 Jun-ichi Kashiwakura and Toshiaki Kawakami
 
-  Genotype and Allele Frequencies of Calcium-Sensing Receptor Gene a986s (rs1801725) Polymorphism in Saudi AdultsResearch Article: J Genet Disor Genet Rep 2016, 5:3
 DOI: 10.4172/2327-5790.1000141
 Sonbol HS and Al Otaibi WF
 
-  Genotype-phenotype characteristics of β thalassemia children in the Gaza Strip, PalestineResearch Article: J Genet Disor Genet Rep 2013, 2:2
 DOI: 10.4172/2327-5790.1000109
 Maged M Yassin, Mahmoud M Sirdah, Rami M Al Haddad, Abdel-Monem H. Lubbad and Mansour S Al-Yazji
 
-  Cleidocranial Dysplasia in a Mother and her New-born DaughterCase Report: J Genet Disor Genet Rep 2016, 5:2
 DOI: 10.4172/2327-5790.1000136
 Ma?gorzata Napieralska, Aleksandra Modlinska, Tomasz Rybkiewicz, Regina ?uralska
 
-  Parental Consanguinity and Birth Defects in Lebanon: The National Collaborative Perinatal Neonatal Network (NCPNN)Research Article: J Genet Disor Genet Rep, 7:3
 DOI: 10.4172/2327-5790.1000181
 Farra C, El Rafei R, Mumtaz G, Charafeddine L, Tlays F and Yunis K
 
-  Morbid Obesity and Psychiatric Disorders Hiding a Sex Aneuploidy: A Case of Late Diagnosis of 48,XXYY SyndromeCase Report: J Genet Disor Genet Rep, 6:3
 DOI: 10.4172/2327-5790.1000162
 Antía Fernández-Pombo, Pablo San Millán-Tejedor, Cristina Guillín-Amarelle, Ana I. Castro, Juan Carlos Guinarte-Cabada, Margarita Ventura-Victoria and David Araújo-Vilar
 
-  Evaluation of Fenitrothion against Culex pipiens (Diptera: Culicidae) Larvae in Grand Tunis Area of TunisiaResearch Article: J Genet Disor Genet Rep, 6:2
 DOI: 10.4172/2327-5790.1000157
 Ahmed Tabbabi, Jaber Daaboub, Ali Lamari, Raja Ben Cheikh, Ibtissem Ben Jha and Hassen Ben Cheikh
 
-  Mini Review: HLA B27 and its Immunogenetics in Ankylosing SpondylitisReview Article: J Genet Disor Genet Rep 2013, 2:1
 DOI: 10.4172/2327-5790.1000104
 Hamid Nawaz Tipu
 
