Asmat Ullah

Asmat Ullah

Postdoc

  • Hansen Group

    Blegdamsvej 3B, Mærsk Tårnet, 8. sal, 2200 København N.

    Phone: +4535321208

Publication year:
All
  1. 2022
  2. Published

    ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment

    Bharadwaj, T., Schrauwen, I., Rehman, S., Liaqat, K., Acharya, A., Giese, A. P. J., Nouel-Saied, L. M., Nasir, A., Everard, J. L., Pollock, L. M., Zhu, S., Bamshad, M. J., Nickerson, D. A., Ali, R. H., Ullah, Asmat, Wali, A., Ali, G., Santos-Cortez, R. L. P., Ahmed, Z. M., McDermott, B. M., Ansar, M., Riazuddin, S., Ahmad, W. & Leal, S. M., 2022, In: European Journal of Human Genetics. 30, p. 22-33

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Accepted/In press

    A novel nonsense variant in EXOC8 underlies a neurodevelopmental disorder

    Ullah, Asmat, Krishin, J., Haider, N., Aurangzeb, B., Abdullah, Suleman, Sufyan, Ahmad, W., Hansen, Torben & Basit, S., 2022, (Accepted/In press) In: Neurogenetics.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. E-pub ahead of print

    Exome sequencing reveals the first intragenic deletion in ABCA5 underlying autosomal recessive hypertrichosis

    Raza, R., Ullah, Asmat, Haider, N., Krishin, J., Shah, M., Khan, F. U., Abdullah, Hansen, Torben, Raza, S. I., Ahmad, W. & Basit, S., 2022, (E-pub ahead of print) In: Clinical and Experimental Dermatology.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. E-pub ahead of print

    Loss of Function Variants in the XPC Causes Severe Xeroderma Pigmentosum in Three Large Consanguineous Families

    Nawal, W., Ullah, Asmat, Ullah, U., Farrakh, K., Ahmad, F., Khan, H., Ahmad, G. S., Khan, B., Ansar, M., Umm-e-Kalsoom & Ahmad, W., 2022, (E-pub ahead of print) In: Klinische Padiatrie. 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 249147337