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

    Open Access
  • 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

    Open Access

    • 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

    Open Access
  • 072
    Paul, Lizzy Teleboshe; Ergoren, Mahmut Cerkez:

    Comparison of Bioinformatics Approaches for Fetal Microdeletions and Monogenic Variations Estimation in Non-invasive Prenatal Testing

    Open Access
  • 076
    Khan, Mahamad Irfanulla; Ahmed, Nadeem; Neela, Praveen Kumar; Unnisa, Nayeem:

    The Human Genetics of Dental Anomalies

    Open Access
  • 082
    Kocaaga, Ayca; Kocaaga, Mustafa:

    Psoriasis: An Immunogenetic Perspective

    Open Access
  • 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

    Open Access

    • Original Article

  • 097
    Huang, Lei; Ding, Zequn; Zhang, Yan:

    CD24+ MDSC-DCs Induced by CCL5-Deficiency Showed Improved Antitumor Activity as Tumor Vaccines

    Open Access
    Supplementary Material (PDF)
  • 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

    Open Access
  • 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

    Open Access
  • 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

    Open Access
  • 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

    Open Access
  • 141
    Zheng, Xinhui; Lv, Liwei; Li, Xiangjun; Jiang, Erlie:

    Efficacy and Safety of Hypomethylating Agents in Chronic Myelomonocytic Leukemia: A Single-Arm Meta-analysis

    Open Access
    Supplementary Material (PDF)
  • 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

    Open Access
  • 159
    Jayaseelan, Vijayashree Priyadharsini; Arumugam, Paramasivam:

    A Computational Data Mining Strategy to Identify the Common Genetic Markers of Temporomandibular Joint Disorders and Osteoarthritis

    Open Access
  • 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

    Open Access

    • Case Report

  • 175
    Alotaibi, Maha; Aldhubaiban, Deema; Alasmari, Ahmed; Alotaibi, Leena:

    A Case of Geroderma Osteodysplasticum Syndrome: Unique Clinical Findings

    Open Access
  • 179
    Kocaaga, Ayca; Yimenicioglu, Sevgi:

    Presentation of an Infant with Chromosome 18p Deletion Syndrome and Asymmetric Septal Hypertrophy

    Open Access

    • 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

    Open Access
  • 185
    Tukek, Tufan; Pehlivan, Sacide; Oyaci, Yasemin; Isoglu-Alkac, Ummuhan:

    Mannose-Binding Lectin 2 Gene Polymorphism during Pandemic: COVID-19 Family

    Open Access

    • Letter to the Editor

  • 189
    Poon, Kok-Siong; Tan, Karen Mei-Ling:

    Pitfalls of PCR-RFLP in Detecting SARS-CoV-2 D614G Mutation

    Open Access