Asmat Ullah
Postdoc
Hansen Group
Blegdamsvej 3B, Mærsk Tårnet, 8. sal, 2200 København N.
1 - 4 out of 4Page size: 25
- 2022
- 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. 22-33Research output: Contribution to journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
ID: 249147337