Clinical Genetics

Cover image for Vol. 92 Issue 4

Edited By: Reiner A. Veitia

Impact Factor: 3.326

ISI Journal Citation Reports © Ranking: 2016: 62/166 (Genetics & Heredity)

Online ISSN: 1399-0004

Just Published Articles

  1. Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis

    L. Papazachariou, G. Papagregoriou, D. Hadjipanagi, P. Demosthenous, K. Voskarides, C. Koutsofti, K. Stylianou, P. Ioannou, D. Xydakis, I. Tzanakis, A. Papadaki, N. Kallivretakis, N. Nikolakakis, G. Perysinaki, D.P. Gale, A. Diamantopoulos, P. Goudas, D. Goumenos, A. Soloukides, I. Boletis, C. Melexopoulou, E. Georgaki, E. Frysira, F. Komianou, D. Grekas, C. Paliouras, P. Alivanis, G. Vergoulas, A. Pierides, E. Daphnis and C. Deltas

    Version of Record online: 25 SEP 2017 | DOI: 10.1111/cge.13077

  2. Hypoglycaemia Represents a Clinically Significant Manifestation of PIK3CA- and CCND2-Associated Segmental Overgrowth

    M.D. JH, N. Hickson, I. Banerjee, P.G. Murray, D. Ram, K. Metcalfe, J. Clayton-Smith and S. Douzgou

    Accepted manuscript online: 23 SEP 2017 09:15AM EST | DOI: 10.1111/cge.13145

  3. Detection of copy number variations in epilepsy using exome data

    N. Tsuchida, M. Nakashima, M. Kato, E. Heyman, T. Inui, K. Haginoya, S. Watanabe, T. Chiyonobu, M. Morimoto, M. Ohta, A. Kumakura, M. Kubota, Y. Kumagai, S.-i. Hamano, C.M. Lourenco, N.A. Yahaya, G.-S. Ch'ng, L.-H. Ngu, A. Fattal-Valevski, M.W. Hubshman, N. Orenstein, D. Marom, L. Cohen, H. Goldberg-Stern, Y. Uchiyama, E. Imagawa, T. Mizuguchi, A. Takata, N. Miyake, H. Nakajima, H. Saitsu, S. Miyatake and N. Matsumoto

    Accepted manuscript online: 22 SEP 2017 10:35AM EST | DOI: 10.1111/cge.13144

  4. INPP5K variant causes autosomal recessive congenital cataract in a Pakistani family

    S. Yousaf, S.A. Sheikh, S. Riazuddin, A.M. Waryah and Z.M. Ahmed

    Accepted manuscript online: 22 SEP 2017 10:15AM EST | DOI: 10.1111/cge.13143

  5. Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palate

    Adrianna Mostowska, Agnieszka Gaczkowska, Kacper Żukowski, Kerstin U. Ludwig, Kamil K. Hozyasz, Piotr Wójcicki, Elizabeth Mangold, Anne C. Böhmer, Stefanie Heilmann-Heimbach, Michael Knapp, Małgorzata Zadurska, Barbara Biedziak, Margareta Budner, Agnieszka Lasota, Agata Daktera-Micker and Paweł P. Jagodziński

    Accepted manuscript online: 19 SEP 2017 10:30AM EST | DOI: 10.1111/cge.13141

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Reiner A. Veitia

Reiner A. Veitia, PhD, is a Professor of Genetics at Paris Diderot University, Paris, France.
Veitia's research focus is primarily on the genetics of premature ovarian insufficiency, nonepithelial ovarian malignancies and the molecular basis of genetic dominance.

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