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1
Clinical and genetic analysis in 185 Chinese probands of osteogenesis imperfecta
Clinical and genetic analysis in 185 Chinese probands of osteogenesis imperfecta
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Clinical and genetic analysis in 185 Chinese probands of osteogenesis imperfecta

Journal of bone and mineral metabolism, 2021-05, Vol.39 (3), p.416-422 [Peer Reviewed Journal]

The Japanese Society Bone and Mineral Research and Springer Japan KK, part of Springer Nature 2020 ;COPYRIGHT 2021 Springer ;The Japanese Society Bone and Mineral Research and Springer Japan KK, part of Springer Nature 2020. ;ISSN: 0914-8779 ;EISSN: 1435-5604 ;DOI: 10.1007/s00774-020-01163-5 ;PMID: 33070251

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2
Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China
Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China
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Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China

Medicine (Baltimore), 2021-04, Vol.100 (17), p.e25647-e25647 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000025647 ;PMID: 33907123

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3
Meta-analysis of association of microRNAs genetic variants with susceptibility to rheumatoid arthritis and systemic lupus erythematosus
Meta-analysis of association of microRNAs genetic variants with susceptibility to rheumatoid arthritis and systemic lupus erythematosus
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Meta-analysis of association of microRNAs genetic variants with susceptibility to rheumatoid arthritis and systemic lupus erythematosus

Medicine (Baltimore), 2021-04, Vol.100 (17), p.e25689-e25689 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000025689 ;PMID: 33907143

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4
Evaluation of association between methylenetetrahydrofolate reductase and azoospermia: A meta-analysis
Evaluation of association between methylenetetrahydrofolate reductase and azoospermia: A meta-analysis
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Evaluation of association between methylenetetrahydrofolate reductase and azoospermia: A meta-analysis

Medicine (Baltimore), 2021-04, Vol.100 (15), p.e24523-e24523 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000024523 ;PMID: 33847607

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5
Commentary on: Analysis of the Molecular Signature of the Breast Implant-Associated Anaplastic Large Cell Lymphoma in an Asian Patient
Commentary on: Analysis of the Molecular Signature of the Breast Implant-Associated Anaplastic Large Cell Lymphoma in an Asian Patient
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Commentary on: Analysis of the Molecular Signature of the Breast Implant-Associated Anaplastic Large Cell Lymphoma in an Asian Patient

Aesthetic surgery journal, 2021-04, Vol.41 (5), p.NP223-NP225 [Peer Reviewed Journal]

ISSN: 1090-820X ;EISSN: 1527-330X ;DOI: 10.1093/asj/sjaa389 ;PMID: 33544150

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6
Association of ST6GAL1 and CYP19A1 polymorphisms in the 3'-UTR with astrocytoma risk and prognosis in a Chinese Han population
Association of ST6GAL1 and CYP19A1 polymorphisms in the 3'-UTR with astrocytoma risk and prognosis in a Chinese Han population
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Association of ST6GAL1 and CYP19A1 polymorphisms in the 3'-UTR with astrocytoma risk and prognosis in a Chinese Han population

BMC cancer, 2021-04, Vol.21 (1), p.391-391, Article 391 [Peer Reviewed Journal]

COPYRIGHT 2021 BioMed Central Ltd. ;2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 1471-2407 ;EISSN: 1471-2407 ;DOI: 10.1186/s12885-021-08110-1 ;PMID: 33836687

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7
Genotype variant screening and phenotypic analysis of FBN1 in Chinese patients with isolated ectopia lentis
Genotype variant screening and phenotypic analysis of FBN1 in Chinese patients with isolated ectopia lentis
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Genotype variant screening and phenotypic analysis of FBN1 in Chinese patients with isolated ectopia lentis

Molecular medicine reports, 2021-04, Vol.23 (4), Article 275

COPYRIGHT 2021 Spandidos Publications ;Copyright Spandidos Publications UK Ltd. 2021 ;Copyright: © Zhou et al. 2021 ;ISSN: 1791-2997 ;EISSN: 1791-3004 ;DOI: 10.3892/mmr.2021.11914 ;PMID: 33576469

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8
Genetic mutations in patients with nonsyndromic hearing impairment of minority and Han Chinese ethnicities in Qinghai, China
Genetic mutations in patients with nonsyndromic hearing impairment of minority and Han Chinese ethnicities in Qinghai, China
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Genetic mutations in patients with nonsyndromic hearing impairment of minority and Han Chinese ethnicities in Qinghai, China

Journal of international medical research, 2021-04, Vol.49 (4), p.3000605211000892-3000605211000892 [Peer Reviewed Journal]

The Author(s) 2021 ;The Author(s) 2021. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 2021 SAGE Publications ;ISSN: 0300-0605 ;EISSN: 1473-2300 ;DOI: 10.1177/03000605211000892 ;PMID: 33827324

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9
Polymorphisms in the DC-SIGN gene and their association with the severity of hand, foot, and mouth disease caused by enterovirus 71
Polymorphisms in the DC-SIGN gene and their association with the severity of hand, foot, and mouth disease caused by enterovirus 71
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Polymorphisms in the DC-SIGN gene and their association with the severity of hand, foot, and mouth disease caused by enterovirus 71

Archives of virology, 2021-04, Vol.166 (4), p.1133-1140 [Peer Reviewed Journal]

The Author(s), under exclusive licence to Springer-Verlag GmbH, AT part of Springer Nature 2021 ;The Author(s), under exclusive licence to Springer-Verlag GmbH, AT part of Springer Nature 2021. ;ISSN: 0304-8608 ;EISSN: 1432-8798 ;DOI: 10.1007/s00705-021-04991-6 ;PMID: 33590343

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10
Association of TNIP1 polymorphisms with hepatocellular carcinoma in a Northwest Chinese Han population
Association of TNIP1 polymorphisms with hepatocellular carcinoma in a Northwest Chinese Han population
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Association of TNIP1 polymorphisms with hepatocellular carcinoma in a Northwest Chinese Han population

Medicine (Baltimore), 2021-03, Vol.100 (12), p.e24843-e24843 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000024843 ;PMID: 33761643

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11
5' UTR CGG repeat expansion in GIPC1 is associated with oculopharyngodistal myopathy
5' UTR CGG repeat expansion in GIPC1 is associated with oculopharyngodistal myopathy
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5' UTR CGG repeat expansion in GIPC1 is associated with oculopharyngodistal myopathy

Brain (London, England : 1878), 2021-03, Vol.144 (2), p.601-614 [Peer Reviewed Journal]

The Author(s) (2020). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For permissions, please email: journals.permissions@oup.com. ;ISSN: 0006-8950 ;EISSN: 1460-2156 ;DOI: 10.1093/BRAIN/AWAA426 ;PMID: 33374016

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12
CCR5 Promoter Polymorphisms Associated With Pulmonary Tuberculosis in a Chinese Han Population
CCR5 Promoter Polymorphisms Associated With Pulmonary Tuberculosis in a Chinese Han Population
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CCR5 Promoter Polymorphisms Associated With Pulmonary Tuberculosis in a Chinese Han Population

Frontiers in immunology, 2021-02, Vol.11, p.544548-544548 [Peer Reviewed Journal]

Copyright © 2021 Liu, Liu, Wang, Zhang, Yao, Zhang and Shi. ;Copyright © 2021 Liu, Liu, Wang, Zhang, Yao, Zhang and Shi 2021 Liu, Liu, Wang, Zhang, Yao, Zhang and Shi ;ISSN: 1664-3224 ;EISSN: 1664-3224 ;DOI: 10.3389/fimmu.2020.544548 ;PMID: 33679683

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13
Mining prognostic markers of Asian hepatocellular carcinoma patients based on the apoptosis-related genes
Mining prognostic markers of Asian hepatocellular carcinoma patients based on the apoptosis-related genes
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Mining prognostic markers of Asian hepatocellular carcinoma patients based on the apoptosis-related genes

BMC cancer, 2021-02, Vol.21 (1), p.175-175, Article 175 [Peer Reviewed Journal]

COPYRIGHT 2021 BioMed Central Ltd. ;COPYRIGHT 2021 BioMed Central Ltd. ;2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 1471-2407 ;EISSN: 1471-2407 ;DOI: 10.1186/s12885-021-07886-6 ;PMID: 33602168

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14
Morphological and genetic heterogeneity of synchronous multifocal lung adenocarcinoma in a Chinese cohort
Morphological and genetic heterogeneity of synchronous multifocal lung adenocarcinoma in a Chinese cohort
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Morphological and genetic heterogeneity of synchronous multifocal lung adenocarcinoma in a Chinese cohort

BMC cancer, 2021-02, Vol.21 (1), p.176-176, Article 176 [Peer Reviewed Journal]

COPYRIGHT 2021 BioMed Central Ltd. ;COPYRIGHT 2021 BioMed Central Ltd. ;2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 1471-2407 ;EISSN: 1471-2407 ;DOI: 10.1186/s12885-021-07892-8 ;PMID: 33602172

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15
Associations between I/D polymorphism in the ACE gene and lung cancer: an updated systematic review and a meta-analysis
Associations between I/D polymorphism in the ACE gene and lung cancer: an updated systematic review and a meta-analysis
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Associations between I/D polymorphism in the ACE gene and lung cancer: an updated systematic review and a meta-analysis

BMC cancer, 2021-02, Vol.21 (1), p.158-158, Article 158 [Peer Reviewed Journal]

COPYRIGHT 2021 BioMed Central Ltd. ;COPYRIGHT 2021 BioMed Central Ltd. ;2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 1471-2407 ;EISSN: 1471-2407 ;DOI: 10.1186/s12885-021-07825-5 ;PMID: 33579229

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16
SPG9A with the new occurrence of an ALDH18A1 mutation in a CMT1A family with PMP22 duplication: case report
SPG9A with the new occurrence of an ALDH18A1 mutation in a CMT1A family with PMP22 duplication: case report
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SPG9A with the new occurrence of an ALDH18A1 mutation in a CMT1A family with PMP22 duplication: case report

BMC neurology, 2021-02, Vol.21 (1), p.64-64, Article 64 [Peer Reviewed Journal]

COPYRIGHT 2021 BioMed Central Ltd. ;2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 1471-2377 ;EISSN: 1471-2377 ;DOI: 10.1186/s12883-021-02087-x ;PMID: 33573605

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17
A Southeast Asian origin for present-day non-African human Y chromosomes
A Southeast Asian origin for present-day non-African human Y chromosomes
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A Southeast Asian origin for present-day non-African human Y chromosomes

Human genetics, 2021-02, Vol.140 (2), p.299-307 [Peer Reviewed Journal]

The Author(s) 2020 ;COPYRIGHT 2020 Springer ;The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/s00439-020-02204-9 ;PMID: 32666166

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18
Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patients
Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patients
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Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patients

Human genetics, 2021-02, Vol.140 (2), p.321-331 [Peer Reviewed Journal]

Springer-Verlag GmbH Germany, part of Springer Nature 2020 ;COPYRIGHT 2020 Springer ;Springer-Verlag GmbH Germany, part of Springer Nature 2020. ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/s00439-020-02207-6 ;PMID: 32710294

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19
Genetic evidence suggests a sense of family, parity and conquest in the Xiongnu Iron Age nomads of Mongolia
Genetic evidence suggests a sense of family, parity and conquest in the Xiongnu Iron Age nomads of Mongolia
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Genetic evidence suggests a sense of family, parity and conquest in the Xiongnu Iron Age nomads of Mongolia

Human genetics, 2021-02, Vol.140 (2), p.349-359 [Peer Reviewed Journal]

Springer-Verlag GmbH Germany, part of Springer Nature 2020 ;COPYRIGHT 2020 Springer ;Springer-Verlag GmbH Germany, part of Springer Nature 2020. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/s00439-020-02209-4 ;PMID: 32734383

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20
Evaluation of ICAM-1 rs5498 and rs3093030 Polymorphisms in Chinese Patients with Colorectal Cancer
Evaluation of ICAM-1 rs5498 and rs3093030 Polymorphisms in Chinese Patients with Colorectal Cancer
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Evaluation of ICAM-1 rs5498 and rs3093030 Polymorphisms in Chinese Patients with Colorectal Cancer

DNA and cell biology, 2021-02, Vol.40 (2), p.384-392 [Peer Reviewed Journal]

Copyright Mary Ann Liebert, Inc. Feb 2021 ;ISSN: 1044-5498 ;EISSN: 1557-7430 ;DOI: 10.1089/dna.2020.6089 ;PMID: 33347388

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