Publications:

Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteome.

Human Genetics

Tollefson, Mallory R MR; Gogal, Rose A RA; Weaver, A Monique AM; Schaefer, Amanda M AM; Marini, Robert J RJ; Azaiez, Hela H; Kolbe, Diana L DL; Wang, Donghong D; Weaver, Amy E AE; Casavant, Thomas L TL; Braun, Terry A TA; Smith, Richard J H RJH; Schnieders, Michael J MJ

Publication Date: 2023-04-22

Variant appearance in text: CHSY1: 1600A>T; Ile534Leu

PubMed Link: 37086329

Variant Present in the following documents:

• 439_2023_2559_MOESM2_ESM.xlsx, sheet 1

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SMAP is a pipeline for sample matching in proteogenomics.

Nature Communications

Li, Ling L; Niu, Mingming M; Erickson, Alyssa A; Luo, Jie J; Rowbotham, Kincaid K; Guo, Kai K; Huang, He H; Li, Yuxin Y; Jiang, Yi Y; Hur, Junguk J; Liu, Chunyu C; Peng, Junmin J; Wang, Xusheng X

Publication Date: 2022-02-08

Variant appearance in text: CHSY1: I534L

PubMed Link: 35136070

Variant Present in the following documents:

• 41467_2022_28411_MOESM4_ESM.xlsx, sheet 1

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Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene.

Nature Communications

Arnadottir, Gudny A GA; Oddsson, Asmundur A; Jensson, Brynjar O BO; Gisladottir, Svanborg S; Simon, Mariella T MT; Arnthorsson, Asgeir O AO; Katrinardottir, Hildigunnur H; Fridriksdottir, Run R; Ivarsdottir, Erna V EV; Jonasdottir, Adalbjorg A; Jonasdottir, Aslaug A; Barrick, Rebekah R; Saemundsdottir, Jona J; le Roux, Louise L; Oskarsson, Gudjon R GR; Asmundsson, Jurate J; Steffensen, Thora T; Gudmundsson, Kjartan R KR; Ludvigsson, Petur P; Jonsson, Jon J JJ; Masson, Gisli G; Jonsdottir, Ingileif I; Holm, Hilma H; Jonasson, Jon G JG; Magnusson, Olafur Th OT; Thorarensen, Olafur O; Abdenur, Jose J; Norddahl, Gudmundur L GL; Gudbjartsson, Daniel F DF; Bjornsson, Hans T HT; Thorsteinsdottir, Unnur U; Sulem, Patrick P; Stefansson, Kari K

Publication Date: 2022-02-04

Variant appearance in text: CHSY1: Ile534Leu

PubMed Link: 35121750

Variant Present in the following documents:

• 41467_2022_28330_MOESM1_ESM.pdf

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Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias.

Genes

Hebert, Eva E; Borngräber, Friederike F; Schmidt, Alexander A; Rakovic, Aleksandar A; Brænne, Ingrid I; Weissbach, Anne A; Hampf, Jennie J; Vollstedt, Eva-Juliane EJ; Größer, Leopold L; Schaake, Susen S; Müller, Michaela M; Manzoor, Humera H; Jabusch, Hans-Christian HC; Alvarez-Fischer, Daniel D; Kasten, Meike M; Kostic, Vladimir S VS; Gasser, Thomas T; Zeuner, Kirsten E KE; Kim, Han-Joon HJ; Jeon, Beomseok B; Bauer, Peter P; Altenmüller, Eckart E; Klein, Christine C; Lohmann, Katja K

Publication Date: 2017-10-18

Variant appearance in text: CHSY1: 1600A>T; I534L; rs141305214

PubMed Link: 29057844

Variant Present in the following documents:

• genes-08-00276-s001.pdf

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