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  1. Coronavirus disease 2019 (COVID-19) caused a series of biological changes in cancer patients which have rendered the original treatment ineffective and increased the difficulty of clinical treatment. However, ...

    Authors: Changpeng Hu, Yue Dai, Huyue Zhou, Jing Zhang, Dandan Xie, Rufu Xu, Mengmeng Yang and Rong Zhang
    Citation: Hereditas 2022 159:45
  2. Nonalcoholic Fatty Liver Disease (NAFLD) is a chronic Liver Disease prevalent all over the world. It has become more and more common in Japan, China and most western developed countries. The global prevalence ...

    Authors: Chun-Yong Sun, Le-Le Yang, Pan Zhao, Pei-Zheng Yan, Jia Li and Dong-Sheng Zhao
    Citation: Hereditas 2022 159:44
  3. Ulcerative colitis (UC) refers to an intractable intestinal inflammatory disease. Its increasing incidence rate imposes a huge burden on patients and society. The UC etiology has not been determined, so screen...

    Authors: Ying Li, Mengyao Tang, Feng Jun Zhang, Yihan Huang, Jing Zhang, Junqi Li, Yunpeng Wang, Jinguang Yang and Shu Zhu
    Citation: Hereditas 2022 159:42
  4. ATM (ataxia-telangiectasia mutated) protein kinase is highly conserved in metazoan, and plays a critical role at DNA damage response, oxidative stress, metabolic stress, immunity, RNA biogenesis etc. Systemic ...

    Authors: Jun Liu, Tianyu Jin, Lanxi Ran, Ze Zhao, Rui Zhu, Gangcai Xie and Xiaolin Bi
    Citation: Hereditas 2022 159:41
  5. Endometrial cancer (EC) is the most common gynecologic malignancy in developed countries and its prevalence is increasing. As an emerging therapy with a promising efficacy, immunotherapy has been extensively a...

    Authors: Zesi Liu, Hongxia Yang, Ziyu Chen and Chunli Jing
    Citation: Hereditas 2022 159:40
  6. The prevalence of Alzheimer's disease (AD) varies based on gender. Due to the lack of early stage biomarkers, most of them are diagnosed at the terminal stage. This study aimed to explore sex-specific signalin...

    Authors: Wencan Ji, Ke An, Canjun Wang and Shaohua Wang
    Citation: Hereditas 2022 159:38
  7. C-C chemokine receptor 5 (CCR5) has recently been recognized as an underlying therapeutic target for various malignancies. However, the association of CCR5 with prognosis in the head and neck squamous cell car...

    Authors: Chunhong Li, Shanlin Chen, Chuanyu Liu, Chune Mo, Weiwei Gong, Jiahua Hu, Min He, Lei Xie, Xianliang Hou, Jianhong Tang and Minglin Ou
    Citation: Hereditas 2022 159:37
  8. Diabetic nephropathy (DN) is the major cause of end-stage renal disease worldwide. The mechanism of tubulointerstitial lesions in DN is not fully elucidated. This article aims to identify novel genes and clari...

    Authors: Haiyan Cao, Xiaosheng Rao, Junya Jia, Tiekun Yan and Dong Li
    Citation: Hereditas 2022 159:36
  9. Preeclampsia, a multisystem disorder of unknown etiology, is one of the leading causes of maternal and perinatal morbidity and mortality. Identifying sensitive, noninvasive markers can aid its prevention and i...

    Authors: Gang Zou, Qingfang Ji, Zixiang Geng, Xiling Du, Lingyan Jiang and Te Liu
    Citation: Hereditas 2022 159:35
  10. Inflammation and long noncoding RNAs (lncRNAs) are gradually becoming important in the development of bladder cancer (BC). Nevertheless, the potential of inflammatory response-related lncRNAs (IRRlncRNAs) as a...

    Authors: Fucai Tang, Jiahao Zhang, Zechao Lu, Haiqin Liao, Chuxian Hu, Yuexue Mai, Yongchang Lai, Zeguang Lu, Zhicheng Tang, Zhibiao Li and Zhaohui He
    Citation: Hereditas 2022 159:32
  11. Apple production in Sweden and elsewhere is being threatened by the fungus, Neonectria ditissima, which causes a disease known as European canker. The disease can cause extensive damage and the removal of disease...

    Authors: Heriberto Vélëz, Jonas Skytte af Sätra, Firuz Odilbekov, Salim Bourras, Larisa Garkava-Gustavsson and Kerstin Dalman
    Citation: Hereditas 2022 159:31
  12. Gout is a chronic metabolic disease that seriously affects human health. It is also a major challenge facing the world, which has brought a heavy burden to patients and society. Hyperuricemia (HUA) is the most...

    Authors: Yue-Li Nian and Chong-Ge You
    Citation: Hereditas 2022 159:30
  13. Arecoline is a well-known risk factor for oral submucosal fibrosis and cancer. However, the mechanistic correlation between arecoline and hepatocellular cancer remains elusive. Here, we investigated the effect...

    Authors: Hai Xie, Ren Jing, Xiaoting Liao, Haishao Chen, Xianlong Xie, Huijun Dai and Linghui Pan
    Citation: Hereditas 2022 159:29
  14. Sepsis is a life-threatening multi-organ dysfunction caused by the dysregulated host response to infection. Sepsis remains a major global concern with high mortality and morbidity, while management of sepsis p...

    Authors: Jing-Xiang Zhang, Wei-Heng Xu, Xin-Hao Xing, Lin-Lin Chen, Qing-Jie Zhao and Yan Wang
    Citation: Hereditas 2022 159:27
  15. Human leukocyte antigen (HLA)-A*03, hemochromatosis ancestral haplotype marker, was associated with greater iron overload in hemochromatosis cohorts reported before discovery of the HFE gene. We sought to learn w...

    Authors: James C. Barton, J. Clayborn Barton and Ronald T. Acton
    Citation: Hereditas 2022 159:25
  16. Mechanisms underlying ischemia/reperfusion injury-acute kidney injury (IRI-AKI) are not fully elucidated. We conducted an integrative analysis of IRI-AKI by bioinformatics methods.

    Authors: Ruilian You, Zhige Heyang, Yixin Ma, Peng Xia, Hua Zheng, Jianfeng Lin, Peili Ji and Limeng Chen
    Citation: Hereditas 2022 159:24
  17. Hox proteins finely coordinate antero-posterior axis during embryonic development and through their action specific target genes are expressed at the right time and space to determine the embryo body plan. As ...

    Authors: Gustavo Jiménez-Mejía, Rubén Montalvo-Méndez, Carolina Hernández-Bautista, Claudia Altamirano-Torres, Martha Vázquez, Mario Zurita and Diana Reséndez-Pérez
    Citation: Hereditas 2022 159:23
  18. Ancestry informative markers are regarded as useful tools for inferring the ancestral information of an individual, which have been widely used in the criminal investigations and population genetic studies. Pr...

    Authors: Wei Cui, Shengjie Nie, Yating Fang, Man Chen, Ming Zhao, Qiong Lan, Chunmei Shen and Bofeng Zhu
    Citation: Hereditas 2022 159:22
  19. Ferroptosis, a novel manner of cell death depended on iron ion, contributed to goat mammary epithelial cell dysfunction. Interleukin-6 (IL-6) is a major pro-inflammatory factor during many inflammation-related...

    Authors: Guangqin Zhu, Shaopu Sui, Fengyun Shi and Qinglin Wang
    Citation: Hereditas 2022 159:21
  20. Spindle and kinetochore‑associated complex subunit 3 (SKA3) has recently been considered a key regulator of carcinogenesis. However, the connection between SKA3 and immune cell infiltration remains unknown.

    Authors: Chenyang Wang, Shasha Liu, Xinhong Zhang, Yan Wang, Peng Guan, Fanyou Bu, Hao Wang, Dawen Wang, Yi Fan, Sichuan Hou and Zhilei Qiu
    Citation: Hereditas 2022 159:20
  21. The historian studies revealed during Mendel’s later research period when mainly focusing on the constant hybrid in Hieracium, he had to be intervened to conduct the controlled pollination experiments in Mirabili...

    Authors: Hui Zhang, Xiaoxi Zhao, Fan Zhao, Jianshan Han and Kun Sun
    Citation: Hereditas 2022 159:19
  22. Lysophosphatidic acid (LPA) and its receptors play a key role in regulating cancer progression. Upregulation of LPA receptor 2 (LPAR2) plays a role in carcinogenesis; however, the exact role of LPAR2 in tumors re...

    Authors: Kai Sun, Ri-xin Chen, Jing-zhang Li and Zhan-xiong Luo
    Citation: Hereditas 2022 159:16
  23. The efficacy of moxibustion in treating rheumatoid arthritis is recognized, but its molecular mechanism is still unclear. This study aimed to characterize the molecular map and potential key genes in the proce...

    Authors: Li Zeng, Jing Guo, Ping Du, Shuguang Yu and Haiyan Yin
    Citation: Hereditas 2022 159:15
  24. Sepsis is a life-threatening condition in which the immune response is directed towards the host tissues, causing organ failure. Since sepsis does not present with specific symptoms, its diagnosis is often del...

    Authors: Mingliang Li, He Huang, Chunlian Ke, Lei Tan, Jiezhong Wu, Shilei Xu and Xusheng Tu
    Citation: Hereditas 2022 159:14
  25. A chronic progressive degenerative joint disease, such as osteoarthritis (OA) is positively related to age. The medical economy is facing a major burden, because of the high disability rate seen in patients wi...

    Authors: Yaguang Han, Jun Wu, Zhenyu Gong, Yiqin Zhou, Haobo Li, Yi Chen and Qirong Qian
    Citation: Hereditas 2022 159:10
  26. The goal of this study was to evaluate marker-assisted selection (MAS) in broiler chickens using previously mapped gene regions associated with ascites syndrome incidence. The second-generation MAS products we...

    Authors: Katie Pepper Lee, Nicholas B. Anthony, Sara K. Orlowski and Douglas D. Rhoads
    Citation: Hereditas 2022 159:9
  27. Niemann-Pick disease type C (NPC) is a rare lysosomal neurovisceral storage disease caused by mutations in the NPC 1 (95%) or NPC2 (5%) genes. The products of NPC1 and NPC2 genes play considerable roles in glycol...

    Authors: Rezvan Abtahi, Parvaneh Karimzadeh, Omid Aryani, Diba Akbarzadeh, Shadab Salehpour, Alireza Rezayi, Seyed Hassan Tonekaboni, Reza Zolfaghari Emameh and Massoud Houshmand
    Citation: Hereditas 2022 159:8
  28. This study aimed to explore the mRNA and protein expression of SLC3A2 in laryngeal carcinoma cells and tissues, and functional regulatory mechanism of SLC3A2 in cell ferroptosis of laryngeal carcinoma.

    Authors: Fangxing Wu, Gaoyun Xiong, Zejun Chen, Chenyang Lei, Qianqian Liu and Yundan Bai
    Citation: Hereditas 2022 159:6
  29. To explore the role and effects of the single-nucleotide polymorphisms (SNPs) of the two functionally related indoleamine 2,3-dioxygenase (IDO) isoforms on IDO activity in the Chinese Han ethnic population.

    Authors: Tingming Cao, Guangming Dai, Hongqian Chu, Chengcheng Kong, Huijuan Duan, Na Tian and Zhaogang Sun
    Citation: Hereditas 2022 159:5
  30. Maffucci syndrome (MS, OMIM 166000) is an extremely unusual, nonhereditary, multisystemic disorder that is characterized with multiple enchondromas and vascular lesions, most of which are spindle cell hemangio...

    Authors: Yi Sun, Xindong Fan, Yamin Rao, Zhenfeng Wang, Deming Wang, Xitao Yang, Lianzhou Zheng, Mingzhe Wen, Ren Cai and Lixin Su
    Citation: Hereditas 2022 159:4
  31. MicroRNAs (miRNAs) are involved in the prognosis of nasopharyngeal carcinoma (NPC). This study used clinical data and expression data of miRNAs to develop a prognostic survival signature for NPC patients to de...

    Authors: Bo Tu, Ling Ye, Qingsong Cao, Sisi Gong, Miaohua Jiang and Hui Li
    Citation: Hereditas 2022 159:3
  32. The homeobox gene homeobrain (hbn) is located in the 57B region together with two other homeobox genes, Drosophila Retinal homeobox (DRx) and orthopedia (otp). All three genes encode transcription factors with im...

    Authors: Kirsten Hildebrandt, Dieter Kolb, Christine Klöppel, Petra Kaspar, Fabienne Wittling, Olga Hartwig, Jannic Federspiel, India Findji and Uwe Walldorf
    Citation: Hereditas 2022 159:2
  33. PIK3CA-related overgrowth spectrum (PROS) is a series of congenital, sporadic disorders that are associated with segmental overgrowth phenotypes and postzygotic, somatic gene mutations in the PIK3CA-ATK-mTOR pat...

    Authors: Li Xin Su, Yi Sun, Zhenfeng Wang, Deming Wang, Xitao Yang, Lianzhou Zheng, Mingzhe Wen, Xindong Fan and Ren Cai
    Citation: Hereditas 2022 159:1
  34. Indian Hedgehog (IHH), an important cell signaling protein, plays a key regulatory role in development of cartilage and chondrogenesis. Earlier studies have shown that heterozygous missense mutations in IHH gene ...

    Authors: Wei Zhou, Luan Chen, Hao Wu, Ting Wang, Gang Ma, Baocheng Wang, Cong Wang, Na Zhang, Yingtian Zhang, Lin He, Shengying Qin, Xiaofang Sun, Hai Zhang and Lu Shen
    Citation: Hereditas 2021 158:48
  35. Asthma is a common chronic respiratory disease that influences 300 million people all over the world. However, the pathogenesis of asthma has not been fully elucidated. It has been reported that transforming g...

    Authors: Yuebin Wang, Huike Yang, Xian Su, Anqiang Cao, Feng Chen, Peng Chen, Fangtao Yan and Huirong Hu
    Citation: Hereditas 2021 158:47
  36. Developmental stuttering is the most common form of stuttering without apparent neurogenic or psychogenic impairment. Recently, whole-exome sequencing (WES) has been suggested to be a promising approach to stu...

    Authors: Yimin Sun, Yong Gao, Yuxi Zhou, Yulong Zhou, Ying Zhang, Dong Wang and Li-Hai Tan
    Citation: Hereditas 2021 158:46

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