DOI: 10.1055/s-00046370

Global Medical Genetics

Ausgabe 02 · Volume 09 · Juni 2022 DOI: 10.1055/s-012-53944

Editorial

057
Ruan, Ji: Quantitative In Vivo Genetic Analysis Reveals Novel Genetic Determinants of Tumor Initiation, Overall Growth, and Exceptional Growth in KRAS-Driven Lung Cancer
060
Qiu, Haibo: Genomic and Immunologic Markers of Intrinsic Resistance to Pembrolizumab Monotherapy in Microsatellite Instability-High Gastric Cancer: Observations from a Prospective Phase II Study

Review Article

063
Rizvi, Aliya A.; Abbas, Mohammad; Verma, Sushma; Verma, Shrikant; Khan, Almas; Raza, Syed T.; Mahdi, Farzana: Determinants in Tailoring Antidiabetic Therapies: A Personalized Approach
072
Paul, Lizzy Teleboshe; Ergoren, Mahmut Cerkez: Comparison of Bioinformatics Approaches for Fetal Microdeletions and Monogenic Variations Estimation in Non-invasive Prenatal Testing
076
Khan, Mahamad Irfanulla; Ahmed, Nadeem; Neela, Praveen Kumar; Unnisa, Nayeem: The Human Genetics of Dental Anomalies
082
Kocaaga, Ayca; Kocaaga, Mustafa: Psoriasis: An Immunogenetic Perspective
090
Khan, Almas; Abbas, Mohammad; Verma, Sushma; Verma, Shrikant; Rizvi, Aliya Abbas; Haider, Fareya; Raza, Syed Tasleem; Mahdi, Farzana: Genetic Variants and Drug Efficacy in Tuberculosis: A Step toward Personalized Therapy

Original Article

097
Huang, Lei; Ding, Zequn; Zhang, Yan: CD24+ MDSC-DCs Induced by CCL5-Deficiency Showed Improved Antitumor Activity as Tumor Vaccines
Supplementary Material
110
Kenanoglu, Sercan; Kandemir, Nefise; Akalin, Hilal; Gokce, Nuriye; Gol, Mehmet F.; Gultekin, Murat; Koseoglu, Emel; Mirza, Meral; Dundar, Munis: Evaluation of Utilizing the Distinct Genes as Predictive Biomarkers in Late-Onset Alzheimer's Disease
118
Kafshnouchi, Maghsoud; Safari, Marzieh; Khodavirdipour, Amir; Bahador, Abbas; Hashemi, Seyed Hamid; Alikhani, Mohammad Sina; Saidijam, Massoud; Alikhani, Mohammad Yousef: Molecular Detection of blaOXA-type Carbapenemase Genes and Antimicrobial Resistance Patterns among Clinical Isolates of Acinetobacter baumannii
124
Sills, E. Scott; Wood, Samuel H.: Phenotype from SAMD9 Mutation at 7p21.2 Appears Attenuated by Novel Compound Heterozygous Variants at RUNX2 and SALL1
129
Pratap, Pushpendra D.; Raza, Syed Tasleem; Zaidi, Ghazala; Kunwar, Shipra; Ahmad, Sharique; Charles, Mark Rector; Eba, Ale; Rajput, Muneshwar: Genetic Variants in Interleukin-10 Gene Association with Susceptibility and Cervical Cancer Development: A Case Control Study
141
Zheng, Xinhui; Lv, Liwei; Li, Xiangjun; Jiang, Erlie: Efficacy and Safety of Hypomethylating Agents in Chronic Myelomonocytic Leukemia: A Single-Arm Meta-analysis
Supplementary Material
152
Hegde, Smita; Hegde, Rajat; Kulkarni, Suyamindra S.; Das, Kusal K.; Gai, Pramod B.; Bulagouda, Rudragouda S.: Analysis of Genetic Variations in Connexin 26 (GJB2) Gene among Nonsyndromic Hearing Impairment: Familial Study
159
Jayaseelan, Vijayashree Priyadharsini; Arumugam, Paramasivam: A Computational Data Mining Strategy to Identify the Common Genetic Markers of Temporomandibular Joint Disorders and Osteoarthritis
166
Xie, Xiaolei; Chai, Hongyan; DiAdamo, Autumn; Grommisch, Brittany; Wen, Jiadi; Zhang, Hui; Li, Peining: Genotype–Phenotype Correlations for Putative Haploinsufficient Genes in Deletions of 6q26-q27: Report of Eight Patients and Review of Literature

Case Report

175
Alotaibi, Maha; Aldhubaiban, Deema; Alasmari, Ahmed; Alotaibi, Leena: A Case of Geroderma Osteodysplasticum Syndrome: Unique Clinical Findings
179
Kocaaga, Ayca; Yimenicioglu, Sevgi: Presentation of an Infant with Chromosome 18p Deletion Syndrome and Asymmetric Septal Hypertrophy

Rapid Communication

182
Kanduc, Darja: Nucleotide Sequence Sharing between the Human Genome and Primers for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Detection
185
Tukek, Tufan; Pehlivan, Sacide; Oyaci, Yasemin; Isoglu-Alkac, Ummuhan: Mannose-Binding Lectin 2 Gene Polymorphism during Pandemic: COVID-19 Family

Letter to the Editor

189
Poon, Kok-Siong; Tan, Karen Mei-Ling: Pitfalls of PCR-RFLP in Detecting SARS-CoV-2 D614G Mutation