Publications:

The prevalence, genetic complexity and population-specific founder effects of human autosomal recessive disorders.

Npj Genomic Medicine

Xiao, Qingyang Q; Lauschke, Volker M VM

Publication Date: 2021-06-02

Variant appearance in text: ABCA4: 5460+1G>C; rs61753030

PubMed Link: 34078906

Variant Present in the following documents:

• 41525_2021_203_MOESM2_ESM.xlsx, sheet 1

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Unique Variant Spectrum in a Jordanian Cohort with Inherited Retinal Dystrophies.

Genes

Azab, Bilal B; Dardas, Zain Z; Aburizeg, Dunia D; Al-Bdour, Muawyah M; Abu-Ameerh, Mohammed M; Saleh, Tareq T; Barham, Raghda R; Maswadi, Ranad R; Ababneh, Nidaa A NA; Alsalem, Mohammad M; Zouk, Hana H; Amr, Sami S; Awidi, Abdalla A

Publication Date: 2021-04-19

Variant appearance in text: rs61753030

PubMed Link: 33921607

Variant Present in the following documents:

• Main text

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Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.

Nature Neuroscience

Genovese, Giulio G; Fromer, Menachem M; Stahl, Eli A EA; Ruderfer, Douglas M DM; Chambert, Kimberly K; Landén, Mikael M; Moran, Jennifer L JL; Purcell, Shaun M SM; Sklar, Pamela P; Sullivan, Patrick F PF; Hultman, Christina M CM; McCarroll, Steven A SA

Publication Date: 2016-11

Variant appearance in text: ABCA4: 5460+1G>C

PubMed Link: 27694994

Variant Present in the following documents:

• NIHMS815183-supplement-supp_table3.xlsx, sheet 1

View BVdb publication page