Connection

Hafiz Muhammad Jafar Hussain to Female

This is a "connection" page, showing publications Hafiz Muhammad Jafar Hussain has written about Female.
Connection Strength

0.034
  1. Whole Exome Sequencing Revealed a Novel Nonsense Variant in the GNRHR Gene Causing Normosmic Hypogonadotropic Hypogonadism in a Pakistani Family. Horm Res Paediatr. 2019; 91(1):9-16.
    View in: PubMed
    Score: 0.018
  2. Comparative analysis of in-silico tools in identifying pathogenic variants in dominant inherited retinal diseases. Hum Mol Genet. 2024 05 18; 33(11):945-957.
    View in: PubMed
    Score: 0.007
  3. Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family. J Gene Med. 2021 01; 23(1):e3279.
    View in: PubMed
    Score: 0.005
  4. CDKN2A/P16INK4A variants association with breast cancer and their in-silico analysis. Breast Cancer. 2019 Jan; 26(1):11-28.
    View in: PubMed
    Score: 0.004
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.