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遺伝性疾患および遺伝レポートのジャーナル |オープンアクセスジャーナル
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class="font-size-30 fweight-400 color-white">遺伝障害と遺伝レポートのジャーナル </h1> </div> </div> </div> </div> <nav class="navbar navbar-expand-lg bg-navbar navbar-light mega-menu journal-menu topbar-shadow" id="mainNavbar"> <div class="container"> <button class="navbar-toggler" type="button" data-bs-toggle="collapse" data-bs-target="#navbarSupportedContent" aria-controls="navbarSupportedContent" aria-expanded="false" aria-label="Toggle navigation"> <span class="navbar-toggler-icon"></span> </button> <div class="collapse navbar-collapse justify-content-center" id="navbarSupportedContent"> <ul class="navbar-nav mb-auto mb-2 mb-lg-0"> <li class="nav-item"><a class="nav-link" href="https://japanese.scitechnol.com/journals/genetic-disorders-genetic-reports.html" title="ここをクリック"><i class="fa fa-home" aria-hidden="true"></i></a></li> <li class="nav-item dropdown"> <a class="nav-link dropdown-toggle" href="#" id="navbarDropdown" role="button" data-bs-toggle="dropdown" aria-expanded="false">説明書</a> <ul 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#a13132!important;padding-left:1%;"> <ul class="nav row journal-highlights"> <li class="col-lg-12"> <b>ジャーナル h- インデックス:</b> 6<br> </li> <li class="col-lg-12"> <b>ジャーナルの引用スコア:</b> 0.55 </li> <li class="col-lg-12"> <b>ジャーナルのインパクトファクター:</b> 0.32 </li> </ul> </div> </div> </div> <div class="contnet-home"> <h2>雑誌について</h2> <p><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">Journal of </font></font><a href="https://www.scitechnol.com/genetics-disorders/best-journals-on-genetic-disorders.php" title="遺伝性疾患"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">Genetic Disorders</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;"> and </font></font><a href="https://www.scitechnol.com/genetic-reports/scientific-journals-on-genetic-reports.php" title="遺伝レポート"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">Genetic Reports は</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;"> 査読済みの学術雑誌であり、原著論文、総説論文、症例報告、短いコミュニケーションなどの形式で、発見と現在の開発に関する最も完全で信頼できる情報源を出版することを目的としています。</font></font><a href="https://www.scitechnol.com/genetics/best-journals-on-genetics.php" title="遺伝学"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">遺伝学</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">、 </font></font><a href="https://www.scitechnol.com/medical-genetics/scholarly-articles-on-medical-genetics.php" title="医療遺伝学"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">医療遺伝学</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">のすべての分野で </font><font style="vertical-align: inherit;"> 、世界中の研究者が制限やその他の購読なしでオンラインで自由に利用できるようにします。</font></font></p> <p><strong><a href="https://www.scholarscentral.org/submissions/genetic-disorders-genetic-reports.html"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">原稿はオンライン投稿システム</font></font></a></strong><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">に投稿する </font><font style="vertical-align: inherit;"> か、電子メールの添付ファイルとして編集部 ( </font></font><a href="mailto:manuscript@scitechnol.com"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">manuals@scitechnol.com ) に送信してください。</font></font></a></p> <p><font style="vertical-align: inherit;"><font style="vertical-align: inherit;"> Journal of </font></font><a href="https://www.scitechnol.com/genetics-disorders/research-journals-in-genetic-disorders.php" title="遺伝性疾患"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">Genetic Disorders</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;"> and Genetic Reports は、主に次のようなトピックに焦点を当てています。</font></font></p> <ul> <li><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">突然変異と機能的結果</font></font></li> <li><a href="https://www.scitechnol.com/chromosome/journal-on-chromosome.php" title="染色体"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">染色体</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">、 </font></font><a href="https://www.scitechnol.com/genetics-disorders/genetics-disorders-journals-ranking.php" title="遺伝子"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">遺伝子</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;"> 、 </font></font><a href="https://www.scitechnol.com/dna-variations/journals-on-DNA-variations.php" title="DNAの変異"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">DNA 変異</font></font></a></li> <li><a href="https://www.scitechnol.com/evironmental-genetics/evironmental-genetics.php" title="環境遺伝学"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">環境遺伝学</font></font></a></li> <li><a href="https://www.scitechnol.com/population-genetics/journals-on-population-genetics.php" title="集団遺伝学"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">集団遺伝学</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;"> と </font></font><a href="https://www.scitechnol.com/evolution/journals-on-evolution.php" title="進化"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">進化</font></font></a></li> <li><a href="https://www.scitechnol.com/multifactorial-disorders/journals-on-multifactorial-disorders.php" title="多因子性"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">多因子性</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;"> および </font></font><a href="https://www.scitechnol.com/polygenic-disorders/journals-on-polygenic-disorders.php" title="多遺伝子性"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">多遺伝子性</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;"> （複合）障害</font></font></li> <li><a href="https://www.scitechnol.com/chromosomes/scholarly-articles-on-chromosomes.php" title="染色体"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">染色体</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;"> 異常: 発生率と種類</font></font></li> <li><a href="https://www.scitechnol.com/genetic-conseling/journals-on-genetic-counseling.php" title="遺伝カウンセリング"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">遺伝カウンセリング</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;"> と </font></font><a href="https://www.scitechnol.com/genetic-education/journals-on-genetic-education.php" title="教育"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">教育</font></font></a></li> <li><a href="https://www.scitechnol.com/chromosome-types/journals-on-chromosome-types.php" title="染色体"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">染色体</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;"> 症候群</font></font></li> <li><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">DNA修復におけるエラー</font></font></li> <li><a href="https://www.scitechnol.com/genetics-disorders/best-journals-on-genetic-disorders.php" title="遺伝性疾患"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">遺伝性疾患</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;"> と治療介入</font></font></li> <li><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">バイオインフォマティクス</font></font></li> </ul> <p><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">このジャーナルは、査読プロセスの品質のために編集追跡システムを使用しています。 </font></font><a href="https://www.scholarscentral.org/submissions/genetic-disorders-genetic-reports.html"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">オンライン投稿システムは、</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;"> オンライン原稿投稿、レビューおよび追跡システムのモードです。査読処理は、Journal of </font></font><a href="https://www.scitechnol.com/genetics-disorders/scientific-journals-on-genetics-disorders.php" title="遺伝性疾患"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">Genetic Disorders</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;"> and </font></font><a href="https://www.scitechnol.com/genetic-reports/research-journals-in-genetic-reports.php" title="遺伝レポート"><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">Genetic Reports</font></font></a><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">の編集委員 </font><font style="vertical-align: inherit;"> または外部の専門家によって実行されます。引用可能な原稿を受理するには、少なくとも 2 人の独立した査読者の承認とその後の編集者の承認が必要です。著者は原稿を提出し、システムを通じて進捗状況を追跡できます。査読者は原稿をダウンロードして編集者に意見を送信できます。編集者は、投稿/レビュー/改訂/出版のプロセス全体を管理できます。</font></font></p> <p><strong><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">遺伝性疾患</font></font></strong></p> <p>A <a href="https://www.scitechnol.com/genetics-disorders/best-journals-on-genetic-disorders.php" title="遺伝性疾患">genetic disorder</a> is a genetic problem caused by one or more abnormalities in the <a href="https://www.scitechnol.com/genetics/best-journals-on-genetics.php">genome</a>, especially a condition that is present from birth.</p> <p><strong>Molecular Genetics</strong></p> <p>Molecular <a href="https://www.scitechnol.com/genetics/best-journals-on-genetics.php">genetics</a> is the field of biology and genetics that studies the structure and function of <a href="https://www.scitechnol.com/genetic-reports/genetic-reports-journals.php">genes</a> at a molecular level.</p> <p><strong>Down syndrome</strong></p> <p>Down syndrome is a <a href="https://www.scitechnol.com/genetics-disorders/genetics-disorders-journals.php">genetic disorder</a> caused by the presence of all or part of a third copy of <a href="https://www.scitechnol.com/chromosomes/scholarly-articles-on-chromosomes.php">chromosome</a>. It is typically associated with physical growth delays, characteristic facial features, and mild to moderate intellectual disability.</p> <p><strong>Gene Therapy</strong></p> <p><a href="https://www.scitechnol.com/gene-variations/journals-on-gene-variations.php">Gene therapy</a> is a therapeutic delivery of nucleic acid polymer into a patient’s cell as a drug to treat disease. Gene therapy could be a way to fix a <a href="https://www.scitechnol.com/genetics/best-journals-on-genetics.php">genetic</a> problem at its source.</p> <p><strong>Genetic Medicine</strong></p> <p>Medicine that involves the diagnosis and management of hereditary <a href="https://www.scitechnol.com/genetics-disorders/genetics-disorders-journals.php">disorders</a>. It is the study of genetic mechanisms, including the <a href="https://www.scitechnol.com/genetics/genetics-journals.php">genetic</a> basis of human disease, and the development of genetically based tests and therapies.</p> <p><strong>Personal Genomics</strong></p> <p>It is the branch of <a href="https://www.scitechnol.com/genetics/best-journals-on-genetics.php">genomics</a> concerned with the sequencing and analysis of the genome of an individual and then giving them their <a href="https://www.scitechnol.com/genetics/current-research-in-genetics.php">genomic</a> information.</p> <p><strong>Genetic Brain Disorders</strong></p> <p>A genetic brain disorder is caused by a variation or a <a href="https://www.scitechnol.com/gene-variations/journals-on-gene-variations.php">mutation</a> in a gene. A variation is a different form of a gene. <a href="https://www.scitechnol.com/genetics/genetics-journals.php">Genetic</a> brain disorders specifically affect the development and function of the brain.</p> <p><strong>Autism</strong></p> <p>Autism is <a href="https://www.scitechnol.com/genetics-disorders/genetics-disorders-journals.php">neurodevelopmental disorder</a> characterized by impaired social interaction, verbal and non-verbal communication, and restricted and repetitive behavior. It is a <a href="https://www.scitechnol.com/genetics-epidemiology/journals-on-genetics-epidemiology.php">birth defect</a> and it is treatable.</p> <p><strong>Statistical Genetics</strong></p> <p>Statistical <a href="https://www.scitechnol.com/genetics/best-journals-on-genetics.php">genetics</a> is a scientific field concerned with the development and application of statistical methods for drawing inferences from genetic data. It is most commonly used in the context of human<a href="https://www.scitechnol.com/genetics/current-research-in-genetics.php"> genetics</a>.</p> <p><strong>Medical Genetics</strong><br /> Medical <a href="https://www.scitechnol.com/genetics/best-journals-on-genetics.php">genetics</a> is the specialty of medicine that involves the diagnosis and management of hereditary <a href="https://www.scitechnol.com/genetics-disorders/best-journals-on-genetic-disorders.php">disorders</a>. Medical genetics differs from human genetics.</p> <p><strong>Genetic Epidemiology</strong></p> <p><a href="https://www.scitechnol.com/genetics-epidemiology/journals-on-genetics-epidemiology.php">Genetic Epidemiology</a> is the study of the role of genetic factors in determining the health and disease in families and in populations, and interplay of such <a href="https://www.scitechnol.com/genetics/genetics-journals.php">genetic</a> factors with environmental factors.</p> <p><strong>Mutations & Functional Consequences</strong></p> <p>A <a href="https://www.scitechnol.com/gene-variations/journals-on-gene-variations.php">mutation</a> occurs when a DNA gene is damaged or changed in such a way as to alter the <a href="https://www.scitechnol.com/genetics/genetics-journals.php">genetic</a> message carried by that gene.</p> <p><strong>Chromosomes, Genes and DNA variations</strong></p> <p><a href="https://www.scitechnol.com/gene-variations/journals-on-gene-variations.php">Genetic variation</a> refers to differences between members of the same species or those of different species. <a href="https://www.scitechnol.com/dna-variations/journals-on-DNA-variations.php">Genetic variation</a> also refers to diversity in gene frequencies related to heredity of individuals.</p> <p><strong>Environmental Genetics</strong></p> <p><a href="https://www.scitechnol.com/evironmental-genetics/evironmental-genetics.php">Gene-environment</a> correlations can arise by both casual and non-casual mechanisms. <a href="https://www.scitechnol.com/gene-variations/journals-on-gene-variations.php">Genetic variants</a> influence environmental exposure indirectly via behavior.</p> <p><strong>Population Genetics and Evolution</strong></p> <p>It is a field of <a href="https://www.scitechnol.com/population-genetics/journals-on-population-genetics.php">biology</a> that studies genetic composition of <a href="https://www.scitechnol.com/evolution/journals-on-evolution.php">biological population</a> and the changes in the genetic composition that result from the operation of various factors, including natural selection.</p> <p><strong>Multifactorial and polygenic (complex) disorders</strong></p> <p><a href="https://www.scitechnol.com/multifactorial-disorders/journals-on-multifactorial-disorders.php">Multifactorial disorders</a> involve variations in multiple genes, often coupled with environmental causes. <a href="https://www.scitechnol.com/polygenic-disorders/journals-on-polygenic-disorders.php">Polygenic disorder</a> caused by the combined action of more than one gene.</p> <p><strong>Chromosomal Abnormalities: Incidence & Types</strong></p> <p><a href="https://www.scitechnol.com/chromosomes/scholarly-articles-on-chromosomes.php">Chromosome</a> abnormality is a missing, extra or irregular portion of <a href="https://www.scitechnol.com/chromosome-types/journals-on-chromosome-types.php">chromosomal DNA</a>. There are many types. However, they can be organized into two basic groups. Those are Numerical and structural abnormalities.</p> <p><strong>Genetic Counseling & Education</strong></p> <p><a href="https://www.scitechnol.com/genetic-conseling/journals-on-genetic-counseling.php">Genetic counseling</a> is a communication process, which aims to help individuals, couples and families understand and adapt to the medical, psychological, familial, and reproductive implications of the <a href="https://www.scitechnol.com/genetics/genetics-journals.php">genetic</a> contributions to specific health conditions.</p> <p><strong>Chromosomal Syndromes</strong></p> <p>A syndrome is a set of medical signs and symptoms that are correlated with each other and, often, with a specific <a href="https://www.scitechnol.com/genetic-disorders/current-research-in-genetic-disorders.php">disease</a>. General designation for syndromes due to <a href="https://www.scitechnol.com/chromosomes/scholarly-articles-on-chromosomes.php">chromosomal</a> aberrations; typically associated with mental retardation and multiple congenital anomalies.</p> <p><strong>DNA Repair</strong></p> <p><a href="https://www.scitechnol.com/dna-variations/journals-on-DNA-variations.php">DNA</a> repair is collection of process by which a cell identifies and corrects damage to the DNA molecules that encode its <a href="https://www.scitechnol.com/genetics/best-journals-on-genetics.php">genome</a>.</p> <p><strong><font style="vertical-align: inherit;"><font style="vertical-align: inherit;">迅速な編集実行およびレビュー プロセス (FEE レビュー プロセス):</font></font></strong><br /> <font style="vertical-align: inherit;"><font style="vertical-align: inherit;">Journal of Genetic Disorders & Genetic Reports は、通常の論文処理料金とは別に 99 ドルを追加の前払いで、高速編集実行およびレビュー プロセス (FEE レビュー プロセス) に参加しています。高速編集実行およびレビュー プロセスは、査読者からのレビューだけでなく担当編集者からのレビュー前段階での応答も迅速に得ることができる、記事のための特別なサービスです。著者は投稿後最大 3 日で事前レビューの応答を得ることができ、査読者によるレビュープロセスは最大 5 日で得られ、その後改訂/出版は 2 日で完了します。記事が担当編集者から改訂の通知を受けた場合、前の査読者または代替査読者による外部レビューにさらに 5 日かかります。</font></font><br /> <br /> <font style="vertical-align: inherit;"><font style="vertical-align: inherit;">原稿の受理は、編集チームの考慮事項と独立した査読の処理によって完全に決定され、定期的な査読出版へのルートや迅速な編集レビュープロセスに関係なく、最高の基準が維持されることが保証されます。担当編集者と記事寄稿者は、科学的基準を遵守する責任があります。論文審査手続きの手数料 99 ドルは、論文が拒否または出版が取り下げられた場合でも返金されません。</font></font><br /> <br /> <font style="vertical-align: inherit;"><font style="vertical-align: inherit;">責任著者または機関/組織は、原稿の査読プロセスの料金を支払う責任があります。追加料金レビュープロセスの支払いは、迅速なレビュー処理と迅速な編集上の決定をカバーし、定期的な論文の出版はオンライン出版のためのさまざまな形式での準備をカバーし、HTML、XML、PDF などの多数の永久アーカイブに全文を確実に含めることができます。そしてさまざまなインデックス作成機関にフィードします。</font></font></p> </div> <!-- recent publications --> <div class="bg-color-sky-light"> <div class="content-xs container"> <div class="divider-v4 divider-v4-center-double text-center margin-b-30"> <h2 class="divider-v4-title">最近の記事</h2> </div> <div class="row"> <div class="masonry-grid-item col-md-4"> <article class="news-v1"> <div class="news-v1-heading padding-tb-5"> <p class="news-v1-heading-tag">研究論文</p> <span class="news-v1-element"><i class="news-v1-element-icon fa fa-circle"></i></span> <h3 class="news-v1-heading-title"><a href="https://japanese.scitechnol.com/abstract/involvement-of-precancerous-lesions-risk-factors-in-epigenetic-peculiarity-of-oncogenic-viruses-of-emalphapapillomavirusem-genus-b-24637.html" title="Involvement of Precancerous Lesions Risk Factors in Epigenetic Peculiarity of Oncogenic Viruses of <em>Alphapapillomavirus</em> Genus Based on the CpG Dinucleotides Island Variability">Involvement of Precancerous Lesions Risk Factors in Epigenetic Peculiarity of Oncogenic Viruses of <em>Alphapapillomavirus</em> Genus Based on the CpG Dinucleotides Island Variability</a></h3> <ul class="list-inline blog-sidebar-tags margin-t-10"> <li><a class="btn btn-xs" href="https://japanese.scitechnol.com/abstract/involvement-of-precancerous-lesions-risk-factors-in-epigenetic-peculiarity-of-oncogenic-viruses-of-emalphapapillomavirusem-genus-b-24637.html" title="ここをクリック">抽象的な</a></li> </ul> </div> <div class="news-v1-content padding-tb-5"> <ul class="list-inline news-v1-lists"> <i class="fa fa-user" aria-hidden="true"></i> <li class="news-v1-lists-item"> <p>Embolo Enyegue Elisee Libert*, Ndipho Tatou Christian Kitchener, Awalou Halidou, Ananga Noah Sidonie, Halmata Mohamadou, Godwe Celestion, Eyebe Richard Honore, Evina Evina Basile, Bell Eric Michel and Essame Oyono Jean Louis </p> </li> </ul> </div> </article> </div> <div class="masonry-grid-item col-md-4"> <article class="news-v1"> <div class="news-v1-heading padding-tb-5"> <p class="news-v1-heading-tag">症例報告</p> <span class="news-v1-element"><i class="news-v1-element-icon fa fa-circle"></i></span> <h3 class="news-v1-heading-title"><a href="https://japanese.scitechnol.com/abstract/penile-sebaceous-adenoma-with-sporadic-loss-of-imlh1i-and-ipms2i-protein-expression-a-case-report-and-review-of-literature-24522.html" title="Penile Sebaceous Adenoma with Sporadic Loss of <i>MLH-1</i> and <i>PMS2</i> Protein Expression: A Case Report and Review of Literature">Penile Sebaceous Adenoma with Sporadic Loss of <i>MLH-1</i> and <i>PMS2</i> Protein Expression: A Case Report and Review of Literature</a></h3> <ul class="list-inline blog-sidebar-tags margin-t-10"> <li><a class="btn btn-xs" href="https://japanese.scitechnol.com/abstract/penile-sebaceous-adenoma-with-sporadic-loss-of-imlh1i-and-ipms2i-protein-expression-a-case-report-and-review-of-literature-24522.html" title="ここをクリック">抽象的な</a></li> </ul> </div> <div class="news-v1-content padding-tb-5"> <ul class="list-inline news-v1-lists"> <i class="fa fa-user" aria-hidden="true"></i> <li class="news-v1-lists-item"> <p>Blaire A. 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