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Article

A mouse model of X-linked chronic granulomatous disease for the development of CRISPR/Cas9 gene therapy.
Sevim-Wunderlich, S., Dang, T., Rossius, J., Schnütgen, F. and Kuehn, R.
Genes 15 (6): 706. June 2024

A homozygous AKNA frameshift variant is associated with microcephaly in a Pakistani family.
Waseem, S.S., Moawia, A., Budde, B., Tariq, M., Khan, A., Ali, Z., Khan, S., Iqbal, M., Malik, N.A., Haque, S.U., Altmüller, J., Thiele, H., Hussain, M.S., Cirak, S., Baig, S.M. and Nürnberg, P.
Genes 12 (10): 1494. October 2021

Modifier genes in microcephaly: a report on WDR62, CEP63, RAD50 and PCNT variants exacerbating disease caused by biallelic mutations of ASPM and CENPJ.
Makhdoom, E.U.H., Waseem, S.S., Iqbal, M., Abdullah, U., Hussain, G., Asif, M., Budde, B., Höhne, W., Tinschert, S., Saadi, S.M., Yousaf, H., Ali, Z., Fatima, A., Kaygusuz, E., Khan, A., Jameel, M., Khan, S., Tariq, M., Anjum, I., Altmüller, J., Thiele, H., Höning, S., Baig, S.M., Nürnberg, P. and Hussain, M.S.
Genes 12 (5): 731. May 2021

Genetic spectrum of syndromic and non-syndromic hearing loss in Pakistani families.
Doll, J., Vona, B., Schnapp, L., Rüschendorf, F., Khan, I., Khan, S., Muhammad, N., Alam Khan, S., Nawaz, H., Khan, A., Ahmad, N., Kolb, S.M., Kühlewein, L., Labonne, J.D.J., Layman, L.C., Hofrichter, M.A.H., Röder, T., Dittrich, M., Müller, T., Graves, T.D., Kong, I.K., Nanda, I., Kim, H.G. and Haaf, T.
Genes 11 (11): 1329. 11 November 2020

Viral infection identifies micropeptides differentially regulated in smORF-containing lncRNAs.
Razooky, B.S., Obermayer, B., O'May, J.B. and Tarakhovsky, A.
Genes 8 (8): 206. 21 August 2017

Effect of culture conditions on viability of mouse and rat embryos developed in vitro.
Popova, E., Bader, M. and Krivokharchenko, A.
Genes 2 (2): 332-344. 1 April 2011

Review

A (3D-nuclear) space odyssey: making sense of Hi-C maps.
Mota-Gómez, I. and Lupiáñez, D.G.
Genes 10 (6): 415. 29 May 2019