Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus?

Alejandra Lázaro-Figueroa; Ana Jimena Hernández-Medrano; Diana Berenice Ramírez-Pineda; Andrés Navarro Cadavid; Mary Makarious; Jia Nee Foo; Chelsea X. Alvarado; Sara Bandres-Ciga; Maria Teresa Periñan; Emilia M. Gatto; Marcelo Kauffman; Samson Khachatryan; Zaruhi Tavadyan; Claire E. Shepherd; Julie Hunter; Kishore Kumar; Melina Ellis; Miguel E. Rentería; Sulev Koks; Alexander Zimprich; Artur F. Schumacher-Schuh; Carlos Rieder; Paula Saffie Awad; Vitor Tumas; Sarah Camargos; Edward A. Fon; Oury Monchi; Ted Fon; Benjamin Pizarro Galleguillos; Marcelo Miranda; Maria Leonor Bustamante; Patricio Olguin; Pedro Chana; Beisha Tang; Huifang Shang; Jifeng Guo; Piu Chan; Wei Luo; Gonzalo Arboleda; Jorge Orozco; Marlene Jimenez del Rio; Alvaro Hernandez; Mohamed Salama; Walaa A. Kamel; Yared Z. Zewde; Alexis Brice; Jean Christophe Corvol; Ana Westenberger; Anastasia Illarionova; Rejko Krüger; the Global Parkinson's Genetics Program (GP2)

doi:10.1002/mds.29719

Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus?

Alejandra Lázaro-Figueroa, Ana Jimena Hernández-Medrano, Diana Berenice Ramírez-Pineda, Andrés Navarro Cadavid, Mary Makarious, Jia Nee Foo, Chelsea X. Alvarado, Sara Bandres-Ciga, Maria Teresa Periñan^*, Emilia M. Gatto, Marcelo Kauffman, Samson Khachatryan, Zaruhi Tavadyan, Claire E. Shepherd, Julie Hunter, Kishore Kumar, Melina Ellis, Miguel E. Rentería, Sulev Koks, Alexander ZimprichArtur F. Schumacher-Schuh, Carlos Rieder, Paula Saffie Awad, Vitor Tumas, Sarah Camargos, Edward A. Fon, Oury Monchi, Ted Fon, Benjamin Pizarro Galleguillos, Marcelo Miranda, Maria Leonor Bustamante, Patricio Olguin, Pedro Chana, Beisha Tang, Huifang Shang, Jifeng Guo, Piu Chan, Wei Luo, Gonzalo Arboleda, Jorge Orozco, Marlene Jimenez del Rio, Alvaro Hernandez, Mohamed Salama, Walaa A. Kamel, Yared Z. Zewde, Alexis Brice, Jean Christophe Corvol, Ana Westenberger, Anastasia Illarionova, Rejko Krüger, the Global Parkinson's Genetics Program (GP2)

^*Corresponding author for this work

Transversal Translational Medicine

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	2117-2119
Number of pages	3
Journal	Movement Disorders
Volume	39
Issue number	11
Early online date	12 Aug 2024
DOIs	https://doi.org/10.1002/mds.29719
Publication status	Published - Nov 2024

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Lázaro-Figueroa, A., Hernández-Medrano, A. J., Ramírez-Pineda, D. B., Navarro Cadavid, A., Makarious, M., Foo, J. N., Alvarado, C. X., Bandres-Ciga, S., Periñan, M. T., Gatto, E. M., Kauffman, M., Khachatryan, S., Tavadyan, Z., Shepherd, C. E., Hunter, J., Kumar, K., Ellis, M., Rentería, M. E., Koks, S., ... the Global Parkinson's Genetics Program (GP2) (2024). Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus? Movement Disorders, 39(11), 2117-2119. https://doi.org/10.1002/mds.29719

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title = "Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus?",

author = "Alejandra L{\'a}zaro-Figueroa and Hern{\'a}ndez-Medrano, {Ana Jimena} and Ram{\'i}rez-Pineda, {Diana Berenice} and {Navarro Cadavid}, Andr{\'e}s and Mary Makarious and Foo, {Jia Nee} and Alvarado, {Chelsea X.} and Sara Bandres-Ciga and Peri{\~n}an, {Maria Teresa} and Gatto, {Emilia M.} and Marcelo Kauffman and Samson Khachatryan and Zaruhi Tavadyan and Shepherd, {Claire E.} and Julie Hunter and Kishore Kumar and Melina Ellis and Renter{\'i}a, {Miguel E.} and Sulev Koks and Alexander Zimprich and Schumacher-Schuh, {Artur F.} and Carlos Rieder and Awad, {Paula Saffie} and Vitor Tumas and Sarah Camargos and Fon, {Edward A.} and Oury Monchi and Ted Fon and Galleguillos, {Benjamin Pizarro} and Marcelo Miranda and Bustamante, {Maria Leonor} and Patricio Olguin and Pedro Chana and Beisha Tang and Huifang Shang and Jifeng Guo and Piu Chan and Wei Luo and Gonzalo Arboleda and Jorge Orozco and {del Rio}, {Marlene Jimenez} and Alvaro Hernandez and Mohamed Salama and Kamel, {Walaa A.} and Zewde, {Yared Z.} and Alexis Brice and Corvol, {Jean Christophe} and Ana Westenberger and Anastasia Illarionova and Rejko Kr{\"u}ger and {the Global Parkinson's Genetics Program (GP2)}",

note = "Grants and funding Global Parkinson's Genetics Program (GP2) ",

year = "2024",

month = nov,

doi = "10.1002/mds.29719",

language = "English",

volume = "39",

pages = "2117--2119",

journal = "Movement Disorders",

issn = "0885-3185",

publisher = "John Wiley & Sons Inc.",

number = "11",

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Lázaro-Figueroa, A, Hernández-Medrano, AJ, Ramírez-Pineda, DB, Navarro Cadavid, A, Makarious, M, Foo, JN, Alvarado, CX, Bandres-Ciga, S, Periñan, MT, Gatto, EM, Kauffman, M, Khachatryan, S, Tavadyan, Z, Shepherd, CE, Hunter, J, Kumar, K, Ellis, M, Rentería, ME, Koks, S, Zimprich, A, Schumacher-Schuh, AF, Rieder, C, Awad, PS, Tumas, V, Camargos, S, Fon, EA, Monchi, O, Fon, T, Galleguillos, BP, Miranda, M, Bustamante, ML, Olguin, P, Chana, P, Tang, B, Shang, H, Guo, J, Chan, P, Luo, W, Arboleda, G, Orozco, J, del Rio, MJ, Hernandez, A, Salama, M, Kamel, WA, Zewde, YZ, Brice, A, Corvol, JC, Westenberger, A, Illarionova, A, Krüger, R & the Global Parkinson's Genetics Program (GP2) 2024, 'Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus?', Movement Disorders, vol. 39, no. 11, pp. 2117-2119. https://doi.org/10.1002/mds.29719