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Genome-wide association mapping of black point reaction in common wheat (Triticum aestivum L.)
Genome-wide association mapping of black point reaction in common wheat (Triticum aestivum L.)
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Genome-wide association mapping of black point reaction in common wheat (Triticum aestivum L.)

Liu, Jindong ; He, Zhonghu ; Rasheed, Awais ; Wen, Weie ; Yan, Jun ; Zhang, Pingzhi ; Wan, Yingxiu ; Zhang, Yong ; Xie, Chaojie ; Xia, Xianchun

BMC plant biology, 2017-11, Vol.17 (1), p.220-220, Article 220 [Periódico revisado por pares]

England: BioMed Central Ltd

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2
The Wheat 660K SNP array demonstrates great potential for marker‐assisted selection in polyploid wheat
The Wheat 660K SNP array demonstrates great potential for marker‐assisted selection in polyploid wheat
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The Wheat 660K SNP array demonstrates great potential for marker‐assisted selection in polyploid wheat

Sun, Congwei ; Dong, Zhongdong ; Zhao, Lei ; Ren, Yan ; Zhang, Ning ; Chen, Feng

Plant biotechnology journal, 2020-06, Vol.18 (6), p.1354-1360 [Periódico revisado por pares]

England: John Wiley & Sons, Inc

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3
Redefining synchronous colorectal cancers based on tumor clonality
Redefining synchronous colorectal cancers based on tumor clonality
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Redefining synchronous colorectal cancers based on tumor clonality

Perea, José ; García, Juan L. ; Corchete, Luis ; Lumbreras, Eva ; Arriba, María ; Rueda, Daniel ; Tapial, Sandra ; Pérez, Jessica ; Vieiro, Victoria ; Rodríguez, Yolanda ; Brandáriz, Lorena ; García‐Arranz, Mariano ; García‐Olmo, Damián ; Goel, Ajay ; Urioste, Miguel ; Sarmiento, Rogelio González

International journal of cancer, 2019-04, Vol.144 (7), p.1596-1608 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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4
Genetic evaluation for twin pregnancies using karyotyping and single nucleotide polymorphism array analysis
Genetic evaluation for twin pregnancies using karyotyping and single nucleotide polymorphism array analysis
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Genetic evaluation for twin pregnancies using karyotyping and single nucleotide polymorphism array analysis

Wu, Xiaoqing ; Huang, Baojia ; Xie, Xiaorui ; Cai, Meiying ; Chen, Yuqin ; Liang, Bin ; Shen, Qingmei ; Guo, Danhua ; Lin, Na ; Su, Linjuan ; Xu, Liangpu

Gene, 2024-02, Vol.895, p.148005-148005, Article 148005 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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Genetic identification and characterization of chromosomal regions for kernel length and width increase from tetraploid wheat
Genetic identification and characterization of chromosomal regions for kernel length and width increase from tetraploid wheat
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Genetic identification and characterization of chromosomal regions for kernel length and width increase from tetraploid wheat

Zhou, Jieguang ; Li, Cong ; You, Jianing ; Tang, Huaping ; Mu, Yang ; Jiang, Qiantao ; Liu, Yaxi ; Chen, Guoyue ; Wang, Jirui ; Qi, Pengfei ; Ma, Jun ; Gao, Yutian ; Habib, Ahsan ; Wei, Yuming ; Zheng, Youliang ; Lan, Xiujin ; Ma, Jian

BMC genomics, 2021-09, Vol.22 (1), p.1-706, Article 706 [Periódico revisado por pares]

London: BioMed Central Ltd

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6
High-Risk Neuroblastoma Tumors with 11q-Deletion Display a Poor Prognostic, Chromosome Instability Phenotype with Later Onset
High-Risk Neuroblastoma Tumors with 11q-Deletion Display a Poor Prognostic, Chromosome Instability Phenotype with Later Onset
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High-Risk Neuroblastoma Tumors with 11q-Deletion Display a Poor Prognostic, Chromosome Instability Phenotype with Later Onset

Carén, Helena ; Kryh, Hanna ; Nethander, Maria ; Sjöberg, Rose-Marie ; Träger, Catarina ; Nilsson, Staffan ; Abrahamsson, Jonas ; Kogner, Per ; Martinsson, Tommy ; Klein, George

Proceedings of the National Academy of Sciences - PNAS, 2010-03, Vol.107 (9), p.4323-4328 [Periódico revisado por pares]

United States: National Academy of Sciences

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7
Genomic loss of HLA alleles may affect the clinical outcome in low-risk myelodysplastic syndrome patients
Genomic loss of HLA alleles may affect the clinical outcome in low-risk myelodysplastic syndrome patients
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Genomic loss of HLA alleles may affect the clinical outcome in low-risk myelodysplastic syndrome patients

Montes, Paola ; Kerick, Martin ; Bernal, Mónica ; Hernández, Francisca ; Jiménez, Pilar ; Garrido, Pilar ; Márquez, Ana ; Jurado, Manuel ; Martin, Javier ; Garrido, Federico ; Ruiz-Cabello, Francisco

Oncotarget, 2018-12, Vol.9 (97), p.36929-36944

United States: Impact Journals LLC

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8
Fetal genetic findings by chromosomal microarray analysis and karyotyping for fetal growth restriction without structural malformations at a territory referral center: 10-year experience
Fetal genetic findings by chromosomal microarray analysis and karyotyping for fetal growth restriction without structural malformations at a territory referral center: 10-year experience
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Fetal genetic findings by chromosomal microarray analysis and karyotyping for fetal growth restriction without structural malformations at a territory referral center: 10-year experience

Wu, Xiaoqing ; He, Shuqiong ; Li, Ying ; Guo, Danhua ; Chen, Xuemei ; Liang, Bin ; Wang, Meiying ; Huang, Hailong ; Xu, Liangpu

BMC Pregnancy and Childbirth, 2023-01, Vol.23 (1), p.73-73, Article 73 [Periódico revisado por pares]

England: BioMed Central Ltd

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9
Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies
Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies
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Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies

Lesch, Klaus-Peter ; Timmesfeld, Nina ; Renner, Tobias J. ; Halperin, Rebecca ; Röser, Christoph ; Nguyen, T. Trang ; Craig, David W. ; Romanos, Jasmin ; Heine, Monika ; Meyer, Jobst ; Freitag, Christine ; Warnke, Andreas ; Romanos, Marcel ; Schäfer, Helmut ; Walitza, Susanne ; Reif, Andreas ; Stephan, Dietrich A. ; Jacob, Christian

Journal of Neural Transmission, 2008-11, Vol.115 (11), p.1573-1585 [Periódico revisado por pares]

Vienna: Springer Vienna

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10
Prenatal diagnosis of non-mosaic sex chromosome abnormalities: a 10-year experience from a tertiary referral center
Prenatal diagnosis of non-mosaic sex chromosome abnormalities: a 10-year experience from a tertiary referral center
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Prenatal diagnosis of non-mosaic sex chromosome abnormalities: a 10-year experience from a tertiary referral center

Wu, Xiaoqing ; Guo, Danhua ; Li, Ying ; Xie, Xiaorui ; Su, Linjuan ; Cai, Meiying ; Zheng, Lin ; Lin, Na ; Liang, Bin ; Huang, Hailong ; Xu, Liangpu

Journal of perinatal medicine, 2023-09, Vol.51 (7), p.904-912 [Periódico revisado por pares]

Germany: De Gruyter

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