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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Disease and GLRB[original query]
A logical relationship for schizophrenia, bipolar, and major depressive disorder. Part 4: Evidence from chromosome 4 high-density association screen.
The Journal of comparative neurology 2019 Feb 527 (2): 392-405.
Tang Jian, Chen Xing, Cai Bin, Chen Ga
Anxiety and Startle Phenotypes in Glrb Spastic and Glra1 Spasmodic Mouse Mutants.
Frontiers in molecular neuroscience 2020 13 152.
Schaefer Natascha, Signoret-Genest Jérémy, von Collenberg Cora R, Wachter Britta, Deckert Jürgen, Tovote Philip, Blum Robert, Villmann Carm
Hereditary Hyperekplexia in Saudi Arabia.
Pediatric neurology 2022 7 134 78-82.
Aldhilan Amal, Alhakeem Afnan, Al Hajjaj Sumayah, Abukhalid Musaad, Aldhalaan Hisham, Salah Ehab, Saeed Muhammed, Tabassum Sadia, El Khashab Heba Y, Aljabri Mohammed, Ali El-Sayed, Alwadei Ali, Hundallah Khalid, Alghamdi Abdulaziz, Hakami Wejdan, AlShafi Shatha, Alkuraya Fowzan S, Alanazy Naif, Seidahmed Mohammed Zain, Alfadhel Majid, Tabarki Brah
Dual role of dysfunctional Asc-1 transporter in distinct human pathologies - human startle disease and developmental delay.
eNeuro 2023 10 .
Paul Drehmann, Sinem Milanos, Natascha Schaefer, Vikram Kasaragod, Sarah Herterich, Ulrike Holzbach-Eberle, Robert J Harvey, Carmen Villma
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