Peter Jin

2021

Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy (Nature Genetics, (2020), 52, 10, (1046-1056), 10.1038/s41588-020-0695-1)

Jin, S. C., Lewis, S. A., Bakhtiari, S., Zeng, X., Sierant, M. C., Shetty, S., Nordlie, S. M., Elie, A., Corbett, M. A., Norton, B. Y., van Eyk, C. L., Haider, S., Guida, B. S., Magee, H., Liu, J., Pastore, S., Vincent, J. B., Brunstrom-Hernandez, J., Papavasileiou, A. & Fahey, M. C. & 57 others, Berry, J. G., Harper, K., Zhou, C., Zhang, J., Li, B., Zhao, H., Heim, J., Webber, D. L., Frank, M. S. B., Xia, L., Xu, Y., Zhu, D., Zhang, B., Sheth, A. H., Knight, J. R., Castaldi, C., Tikhonova, I. R., López-Giráldez, F., Keren, B., Whalen, S., Buratti, J., Doummar, D., Cho, M., Retterer, K., Millan, F., Wang, Y., Waugh, J. L., Rodan, L., Cohen, J. S., Fatemi, A., Lin, A. E., Phillips, J. P., Feyma, T., MacLennan, S. C., Vaughan, S., Crompton, K. E., Reid, S. M., Reddihough, D. S., Shang, Q., Gao, C., Novak, I., Badawi, N., Wilson, Y. A., McIntyre, S. J., Mane, S. M., Wang, X., Amor, D. J., Zarnescu, D. C., Lu, Q., Xing, Q., Zhu, C., Bilguvar, K., Padilla-Lopez, S., Lifton, R. P., Gecz, J., MacLennan, A. H. & Kruer, M. C., Mar 2021, In: Nature Genetics. 53, 3, p. 412 1 p.

Research output: Contribution to journal › Comment/debate

Open Access

1 Scopus citations

Erratum: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia (Brain (2021) 144:5 (1422-1434) DOI: 10.1093/brain/awab041)

Wiessner, M., Maroofian, R., Ni, M. Y., Pedroni, A., Müller, J. S., Stucka, R., Beetz, C., Efthymiou, S., Santorelli, F. M., Alfares, A. A., Zhu, C., Uhrova Meszarosova, A., Alehabib, E., Bakhtiari, S., Janecke, A. R., Otero, M. G., Chen, J. Y. H., Peterson, J. T., Strom, T. M. & De Jonghe, P. & 86 others, Deconinck, T., De Ridder, W., De Winter, J., Pasquariello, R., Ricca, I., Alfadhel, M., Van De Warrenburg, B. P., Portier, R., Bergmann, C., Ghasemi Firouzabadi, S., Jin, S. C., Bilguvar, K., Hamed, S., Abdelhameed, M., Haridy, N. A., Maqbool, S., Rahman, F., Anwar, N., Carmichael, J., Pagnamenta, A. T., Wood, N. W., Tran Mau-Them, F., Haack, T., Di Rocco, M., Ceccherini, I., Iacomino, M., Zara, F., Salpietro, V., Scala, M., Rusmini, M., Xu, Y., Wang, Y., Suzuki, Y., Koh, K., Nan, H., Ishiura, H., Tsuji, S., Lambert, L., Schmitt, E., Lacaze, E., Küpper, H., Dredge, D., Skraban, C., Goldstein, A., Willis, M. J. H., Grand, K., Graham, J. M., Lewis, R. A., Millan, F., Duman, Ö., Olgac Dundar, N., Uyanik, G., Schöls, L., Nürnberg, P., Nürnberg, G., Català-Bordes, A., Seeman, P., Kuchar, M., Darvish, H., Rebelo, A., Bouçanova, F., Medard, J. J., Chrast, R., Auer-Grumbach, M., Alkuraya, F. S., Shamseldin, H., Al Tala, S., Rezazadeh Varaghchi, J., Najafi, M., Deschner, S., Gläser, D., Hüttel, W., Kruer, M. C., Kamsteeg, E. J., Takiyama, Y., Züchner, S., Baets, J., Synofzik, M., Schüle, R., Horvath, R., Houlden, H., Bartesaghi, L., Lee, H. J., Ampatzis, K., Pierson, T. M. & Senderek, J., Aug 1 2021, In: Brain. 144, 8, p. E70

Research output: Contribution to journal › Comment/debate

Open Access

1 Scopus citations

2019

Erratum: Mutations in TFAP2B and previously unim-plicated genes of the BMP, Wnt, and Hedgehog pathways in syndromic craniosynostosis (Proceedings of the National Academy of Sciences of the United States of America 116 (15116–15121) DOI: 10.1073/pnas.1902041116)

Timberlake, A. T., Jin, S. C., Nelson-Williams, C., Wu, R., Furey, C. G., Islam, B., Haider, S., Loring, E., Galm, A., Steinbacher, D. M., Larysz, D., Staffenberg, D. A., Flores, R. L., Rodriguez, E. D., Boggon, T. J., Persing, J. A. & Lifton, R. P., Aug 20 2019, In: Proceedings of the National Academy of Sciences of the United States of America. 116, 34, p. 17130 1 p.

Research output: Contribution to journal › Comment/debate

Open Access

Erratum: De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias (The American Journal of Human Genetics (2018) 103(5) (666–678), (S0002929718303173), (10.1016/j.ajhg.2018.09.006))

Task Force for Neonatal Genomics & Deciphering Developmental Disorders Study, Mar 7 2019, In: American journal of human genetics. 104, 3, p. 562 1 p.

Research output: Contribution to journal › Comment/debate

Open Access

8 Scopus citations

2010

Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 (Nat. Genet. (2010) 42 (525-529))

Beaty, T. H., Murray, J. C., Marazita, M. L., Munger, R. G., Hetmanski, I. R. J. B., Liang, K. Y., Wu, T., Murray, T., Fallin, M. D., Redett, R. A., Raymond, G., Schwender, H., Jin, S. C., Cooper, M. E., Dunnwald, M., Mansilla, M. A., Leslie, E., Bullard, S., Lidral, A. C. & Moreno, L. M. & 32 others, Menezes, R., Vieira, A. R., Petrin, A., Wilcox, A. J., Lie, R. T., Jabs, E. W., Wu-Chou, Y. H., Chen, P. K., Wang, H., Ye, X., Huang, S., Yeow, V., Chong, S. S., Jee, S. H., Shi, B., Christensen, K., Melbye, M., Doheny, K. F., Pugh, E. W., Ling, H., Castilla, E. E., Czeizel, A. E., Ma, L., Field, L. L., Brody, L., Pangilinan, F., Mills, J. L., Molloy, A. M., Kirke, P. N., Scott, J. M., Arcos-Burgos, M. & Scott, A. F., Aug 2010, In: Nature Genetics. 42, 8, p. 727 1 p.

Research output: Contribution to journal › Comment/debate

Open Access

3 Scopus citations

Peter Jin

Research output

Search results

Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy (Nature Genetics, (2020), 52, 10, (1046-1056), 10.1038/s41588-020-0695-1)

Erratum: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia (Brain (2021) 144:5 (1422-1434) DOI: 10.1093/brain/awab041)

Erratum: Mutations in TFAP2B and previously unim-plicated genes of the BMP, Wnt, and Hedgehog pathways in syndromic craniosynostosis (Proceedings of the National Academy of Sciences of the United States of America 116 (15116–15121) DOI: 10.1073/pnas.1902041116)

Erratum: De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias (The American Journal of Human Genetics (2018) 103(5) (666–678), (S0002929718303173), (10.1016/j.ajhg.2018.09.006))

Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 (Nat. Genet. (2010) 42 (525-529))