Genetic scores for adult subcortical volumes associate with subcortical volumes during infancy and childhood

by Ikram, M.A, Jansen, P.R, Labrecque, J.A, Lamballais, S., White, T.
Published 2021

Targeted resequencing showing novel common and rare genetic variants increases the risk of asthma in the Chinese Han population

by Cheng, Z., Deng, Y., Fang, S., Li, J., Li, Z., Liu, J., Luo, G., Luo, L., Mo, B., Shu, Y., Wang, Y., Wang, Z., Wei, J., Xiong, W., Yang, H., Yang, J., Yu, B., Zhang, X., Zhu, J.
Published 2021

Association between the TAP1 gene polymorphisms and recurrent respiratory papillomatosis in patients from Western Mexico: A pilot study

by Araujo-Caballero, V., Cazarez-Navarro, G., Govea-Camacho, L.H, Hernandez-Cañaveral, I.I, Martinez-Lopez, E., Muñoz-Valle, J.F, Ortiz-Hernandez, E., Palomares-Marin, J., Rodriguez-Preciado, S.Y
Published 2021

Application of high-throughput sequencing for hereditary thrombocytopenia in southwestern China

by Dou, Y., Guan, X., Guo, Y., Luo, M., Wen, X., Xian, Y., Yu, J., Zhang, L.
Published 2021

Transmission patterns of Streptococcus mutans demonstrated by a combined rep-PCR and MLST approach

by Childers, N.K, Momeni, S.S, Moser, S.A, Whiddon, J.
Published 2018

Biogenetic ties and parent-child relationships: The misplaced critique

by Murphy, T.F
Published 2019

Mortality in parents after the death of a child

by Floyd, F.J, Greenberg, J.S, Mailick, M.R, Song, J.
Published 2019

Expression of aquaporin 3 and 5 as a potential marker for distinguishing dry mouth from Sjögren’s syndrome

by Hideshima, K., Ichiyama, T., Nakatani, E., Nariai, Y., Sekine, J., Tatsumi, K., Urano, T.
Published 2018

Novel factor VII gene mutations in six families with hereditary coagulation factor VII deficiency

by Fang, Y., Feng, Q., Leng, S., Peng, J., Sheng, Z., Wang, S., Xu, S., Zhang, L., Zhang, X., Zhang, X., Zhang, Y.
Published 2021

Transcription factor FOXA3 promotes the development of Hepatoblastoma via regulating HNF1A, AFP, and ZFHX3 expression

by Zhan, X., Zhao, A.
Published 2021

First molecular epidemiology of Entamoeba histolytica, E. dispar and E. moshkovskii infections in Yemen: different species-specific associated risk factors

by Al-Adhroey, A.H, Al-Areeqi, M.A, Al-Mekhlafi, H.M, Anuar, T.S, Atroosh, W.M, Dawaki, S., Elyana, F.N, Ithoi, I., Lau, Y.-L, Nasr, N.A, Sady, H., Surin, J.
Published 2017

A novel WT1 gene mutation in a chinese girl with denys-drash syndrome

by Cai, J., Guan, Z., He, M., Jin, H., Li, L., Mao, J., Shu, Q., Wang, F., Wang, J., Zhao, M., Zhu, K.
Published 2021

The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences

by Arveiler, B., Bagdonaite-Bejaran, L., Bergen, A.A, Birk, O.S, Blumenfeld, A., De Wit, G.C, Florijn, R.J, Fulton, A.B, Gradstein, L., Kruijt, C.C, Lasseaux, E., Perez, Y., Schalij-Delfos, N.E, Van Genderen, M.M, Yahalom, C., Zanlonghi, X.
Published 2022

ALK-positive histiocytosis: a new clinicopathologic spectrum highlighting neurologic involvement and responses to ALK inhibition

by Abla, O., Alexandrescu, S., Allotey, J., Atkinson, M., Barbaro, P.M, Baykov, V.V, Beilken, A., Bonneau-Lagacherie, J., Bornemann, A., Brandt, J.M, Collin, M., Dembowska-Baginska, B., Diamond, E.L, Donadieu, J., Durham, B.H, Ebinger, M., El Demellawy, D., Eldem, I., Emile, J.-F, Empringham, B., Ernestus, K., Evseev, D.A, Farnault, L., Fend, F., Feuerhake, F., Flucke, U.E, Fraitag, S., Garg, S., Gaspari, S., Gessi, M., Grier, D.D, Gryniewicz-Kwiatkowska, O., Haroche, J., Hélias-Rodzewicz, Z., Henry, M.M, Héritier, S., Hiemcke-Jiwa, L., Hogendoorn, P.C.W, Hornick, J.L, Jullié, M.-L, Kemps, P.G, Kumar, A.R, Lamaison, C., Leino, D.G, Lorsbach, R., Madni, M., Massoth, L.R, Méry, T., Möhle, R., Muñoz-Arcos, L.S, Peeke, S.Z, Petrova-Drus, K., Picarsic, J., Picton, S., Potapenko, V., Poulin, A., Raghunathan, A., Rossi, S., Roy, S., Schafernak, K.T, Sciot, R., Sisk, B.A, Sridhar, V., Suchi, M., Swanson, A.A, Tam, I.S, Tamburrini, G., Tiwari, N., Turner, K., van de Wetering, M.D, van den Bos, C., van Halteren, A.G.S, van Laar, J.A.M, van Noesel, C.J.M, Verdijk, R.M, Weinstein, J.L, Whitlock, J.A, Wiegering, V., Woei-A-Jin, F.J.S.H, Yaseen, N.R, Yeo, K.K
Published 2022

ABO blood grouping: A potential risk factor for early childhood caries - A cross-sectional study

by Govindaraju, L., Jeevanandan, G., Subramanian, E.
Published 2018