Find Research Outputs

Search in all content

Filters for Research Output

Search concepts
Selected Filters

Publication Year

  • 2020
  • 2019
  • 2018
  • 2017
  • 2016
  • 2015
  • 2014
  • 2013
  • 2012

Author

  • Stephan L Zuchner
2020

A longitudinal study of CMT1A using Rasch analysis based CMT neuropathy and examination scores

Inherited Neuropathies Consortium—Rare Diseases Clinical Research Network (INC-RDCRN), Mar 3 2020, In : Neurology. 94, 9, p. e884-e896

Research output: Contribution to journalComment/debate

Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

Inherited Neuropathy Consortium, May 1 2020, In : Nature genetics. 52, 5, p. 473-481 9 p.

Research output: Contribution to journalArticle

2 Scopus citations

Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion

Cortese, A., Tozza, S., Yau, W. Y., Rossi, S., Beecroft, S. J., Jaunmuktane, Z., Dyer, Z., Ravenscroft, G., Lamont, P. J., Mossman, S., Chancellor, A., Maisonobe, T., Pereon, Y., Cauquil, C., Colnaghi, S., Mallucci, G., Curro, R., Tomaselli, P. J., Thomas-Black, G., Sullivan, R. & 22 others, Efthymiou, S., Rossor, A. M., Laurá, M., Pipis, M., Horga, A., Polke, J., Kaski, D., Horvath, R., Chinnery, P. F., Marques, W., Tassorelli, C., Devigili, G., Leonardis, L., Wood, N. W., Bronstein, A., Giunti, P., Züchner, S., Stojkovic, T., Laing, N., Roxburgh, R. H., Houlden, H. & Reilly, M. M., 2020, In : Brain. 143, 2, p. 489-490 2 p.

Research output: Contribution to journalArticle

Open Access
3 Scopus citations

Clinical Reasoning: A case of bilateral foot drop in a 74-year-old man

Harada, Y., Zuchner, S. L., Herrmann, D. N. & Veerapandiyan, A., Mar 3 2020, In : Neurology. 94, 9, p. 405-409 5 p.

Research output: Contribution to journalArticle

Open Access

Confirmation of TACO1 as a Leigh Syndrome Disease Gene in Two Additional Families

Oktay, Y., Güngör, S., Zeltner, L., Wiethoff, S., Schöls, L., Sonmezler, E., Yilmaz, E., Munro, B., Bender, B., Kernstock, C., Kaemereit, S., Liepelt, I., Töpf, A., Yis, U., Laurie, S., Yaramis, A., Zuchner, S., Hiz, S., Lochmüller, H., Schüle, R. & 1 others, Horvath, R., 2020, In : Journal of neuromuscular diseases. 7, 3, p. 301-308 8 p.

Research output: Contribution to journalArticle

De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation

Undiagnosed Diseases Network, Apr 2 2020, In : American journal of human genetics. 106, 4, p. 570-583 14 p.

Research output: Contribution to journalArticle

Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease

Buglo, E., Sarmiento, E., Martuscelli, N. B., Sant, D. W., Danzi, M. C., Abrams, A. J., Dallman, J. E. & Züchner, S., 2020, In : PloS one. 15, 3, e0230566.

Research output: Contribution to journalArticle

Open Access

Genetic modifiers and non-Mendelian aspects of CMT

Bis-Brewer, D. M., Fazal, S. & Züchner, S., Jan 1 2020, In : Brain Research. 1726, 146459.

Research output: Contribution to journalReview article

1 Scopus citations

Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutation

Stregapede, F., Travaglini, L., Rebelo, A. P., Cintra, V. P., Bellacchio, E., Bosco, L., Alfieri, P., Pro, S., Zuchner, S., Bertini, E. & Nicita, F., Mar 1 2020, In : Clinical Genetics. 97, 3, p. 521-526 6 p.

Research output: Contribution to journalArticle

Prot2HG: a database of protein domains mapped to the human genome

Stanek, D., Bis-Brewer, D. M., Saghira, C., Danzi, M. C., Seeman, P., Lassuthova, P. & Zuchner, S., Jan 1 2020, In : Database : the journal of biological databases and curation. 2020

Research output: Contribution to journalArticle

Open Access

Publisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein (Nature Neuroscience, (2019), 22, 12, (1966-1974), 10.1038/s41593-019-0530-0)

ALSGENS Consortium, FALS Consortium, Project MinE Consortium & CReATe Consortium, Feb 1 2020, In : Nature Neuroscience. 23, 2, 1 p.

Research output: Contribution to journalComment/debate

Open Access
2019

A network biology approach to unraveling inherited axonopathies

Bis-Brewer, D. M., Danzi, M. C., Wuchty, S. & Züchner, S., Dec 1 2019, In : Scientific reports. 9, 1, 1692.

Research output: Contribution to journalArticle

Open Access
2 Scopus citations

A novel MFN2 mutation causes variable clinical severity in a multi-generational CMT2 family

Dankwa, L., Richardson, J., Motley, W. W., Scavina, M., Courel, S., Bardakjian, T., Züchner, S. & Scherer, S. S., Feb 2019, In : Neuromuscular Disorders. 29, 2, p. 134-137 4 p.

Research output: Contribution to journalArticle

2 Scopus citations

Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia (Nature Genetics, (2019), 51, 4, (649-658), 10.1038/s41588-019-0372-4)

Cortese, A., Simone, R., Sullivan, R., Vandrovcova, J., Tariq, H., Yau, W. Y., Humphrey, J., Jaunmuktane, Z., Sivakumar, P., Polke, J., Ilyas, M., Tribollet, E., Tomaselli, P. J., Devigili, G., Callegari, I., Versino, M., Salpietro, V., Efthymiou, S., Kaski, D., Wood, N. W. & 10 others, Andrade, N. S., Buglo, E., Rebelo, A., Rossor, A. M., Bronstein, A., Fratta, P., Marques, W. J., Züchner, S., Reilly, M. M. & Houlden, H., May 1 2019, In : Nature genetics. 51, 5, 1 p.

Research output: Contribution to journalComment/debate

Open Access
2 Scopus citations

Autosomal dominant optic atrophy and cataract "plus" phenotype including axonal neuropathy

Horga, A., Bugiardini, E., Manole, A., Bremner, F., Jaunmuktane, Z., Dankwa, L., Rebelo, A. P., Woodward, C. E., Hargreaves, I. P., Cortese, A., Pittman, A. M., Brandner, S., Polke, J. M., Pitceathly, R. D. S., Züchner, S., Hanna, M. G., Scherer, S. S., Houlden, H. & Reilly, M. M., Apr 1 2019, In : Neurology: Genetics. 5, 2, e322.

Research output: Contribution to journalArticle

Open Access
1 Scopus citations

Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia

Cortese, A., Simone, R., Sullivan, R., Vandrovcova, J., Tariq, H., Yan, Y. W., Humphrey, J., Jaunmuktane, Z., Sivakumar, P., Polke, J., Ilyas, M., Tribollet, E., Tomaselli, P. J., Devigili, G., Callegari, I., Versino, M., Salpietro, V., Efthymiou, S., Kaski, D., Wood, N. W. & 10 others, Andrade, N. S., Buglo, E., Rebelo, A., Rossor, A. M., Bronstein, A., Fratta, P., Marques, W. J., Züchner, S., Reilly, M. M. & Houlden, H., Apr 1 2019, In : Nature genetics. 51, 4, p. 649-658 10 p.

Research output: Contribution to journalArticle

40 Scopus citations

Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia

Wagner, M., Osborn, D. P. S., Gehweiler, I., Nagel, M., Ulmer, U., Bakhtiari, S., Amouri, R., Boostani, R., Hentati, F., Hockley, M. M., Hölbling, B., Schwarzmayr, T., Karimiani, E. G., Kernstock, C., Maroofian, R., Müller-Felber, W., Ozkan, E., Padilla-Lopez, S., Reich, S., Reichbauer, J. & 9 others, Darvish, H., Shahmohammadibeni, N., Tafakhori, A., Vill, K., Zuchner, S., Kruer, M. C., Winkelmann, J., Jamshidi, Y. & Schüle, R., Dec 1 2019, In : Nature communications. 10, 1, 4790.

Research output: Contribution to journalArticle

Open Access
1 Scopus citations

De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

Undiagnosed Diseases Network, Aug 1 2019, In : American journal of human genetics. 105, 2, p. 413-424 12 p.

Research output: Contribution to journalArticle

2 Scopus citations

Erratum: Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia (The American Journal of Human Genetics (2019) 104(4) (767–773), (S0002929719300977), (10.1016/j.ajhg.2019.03.001))

Farazi Fard, M. A., Rebelo, A. P., Buglo, E., Nemati, H., Dastsooz, H., Gehweiler, I., Reich, S., Reichbauer, J., Quintáns, B., Ordóñez-Ugalde, A., Cortese, A., Courel, S., Abreu, L., Powell, E., Danzi, M. C., Martuscelli, N. B., Bis-Brewer, D. M., Tao, F., Zarei, F., Habibzadeh, P. & 22 others, Yavarian, M., Modarresi, F., Silawi, M., Tabatabaei, Z., Yousefi, M., Farpour, H. R., Kessler, C., Mangold, E., Kobeleva, X., Tournev, I., Chamova, T., Mueller, A. J., Haack, T. B., Tarnopolsky, M., Gan-Or, Z., Rouleau, G. A., Synofzik, M., Sobrido, M. J., Jordanova, A., Schüle, R., Zuchner, S. & Faghihi, M. A., Jun 6 2019, In : American journal of human genetics. 104, 6, 1 p.

Research output: Contribution to journalComment/debate

1 Scopus citations
Open Access
1 Scopus citations

Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein

ALSGENS Consortium, FALS Consortium, Project MinE Consortium & CReATe Consortium, Dec 1 2019, In : Nature Neuroscience. 22, 12, p. 1966-1974 9 p.

Research output: Contribution to journalArticle

7 Scopus citations

FAHN/SPG35: A narrow phenotypic spectrum across disease classifications

Rattay, T. W., Lindig, T., Baets, J., Smets, K., Deconinck, T., Söhn, A. S., Hörtnagel, K., Eckstein, K. N., Wiethoff, S., Reichbauer, J., Döbler-Neumann, M., Krägeloh-Mann, I., Auer-Grumbach, M., Plecko, B., Münchau, A., Wilken, B., Janauschek, M., Giese, A. K., De Bleecker, J. L., Ortibus, E. & 10 others, Debyser, M., Lopez De Munain, A., Pujol, A., Bassi, M. T., D'Angelo, M. G., De Jonghe, P., Züchner, S., Bauer, P., Schöls, L. & Schüle, R., Jun 1 2019, In : Brain. 142, 6, p. 1561-1572 12 p.

Research output: Contribution to journalArticle

4 Scopus citations

Glutathione S-Transferase Regulates Mitochondrial Populations in Axons through Increased Glutathione Oxidation

Smith, G. A., Lin, T. H., Sheehan, A. E., Van der Goes van Naters, W., Neukomm, L. J., Graves, H. K., Bis-Brewer, D. M., Züchner, S. & Freeman, M. R., Jul 3 2019, In : Neuron. 103, 1, p. 52-65.e6

Research output: Contribution to journalArticle

Open Access
5 Scopus citations

Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCs

Manganelli, F., Parisi, S., Nolano, M., Miceli, F., Tozza, S., Pisciotta, C., Iodice, R., Provitera, V., Cicatiello, R., Zuchner, S., Taglialatela, M., Russo, T. & Santoro, L., Dec 1 2019, In : Journal of the Peripheral Nervous System. 24, 4, p. 330-339 10 p.

Research output: Contribution to journalArticle

Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification

Undiagnosed Diseases Network, Jun 6 2019, In : American journal of human genetics. 104, 6, p. 1127-1138 12 p.

Research output: Contribution to journalArticle

5 Scopus citations

Magnetic Resonance Imaging characteristics in case of TOR1AIP1 muscular dystrophy

Undiagnosed Diseases Network (UDN) & Members of the Undiagnosed Diseases Network, Nov 1 2019, In : Clinical Imaging. 58, p. 108-113 6 p.

Research output: Contribution to journalArticle

Modifier gene candidates in charcot-marie-tooth disease type 1A: A case-only genome-wide association study

Tao, F., Beecham, G. W., Rebelo, A. P., Blanton, S. H., Moran, J. J., Lopez-Anido, C., Svaren, J., Abreu, L., Rizzo, D., Kirk, C. A., Wu, X., Feely, S., Verhamme, C., Saporta, M. A., Herrmann, D. N., Day, J. W., Sumner, C. J., Lloyd, T. E., Li, J., Yum, S. W. & 8 others, Taroni, F., Baas, F., Choi, B. O., Pareyson, D., Scherer, S. S., Reilly, M. M., Shy, M. E. & Züchner, S., 2019, In : Journal of neuromuscular diseases. 6, 2, p. 201-211 11 p.

Research output: Contribution to journalArticle

1 Scopus citations

MOVR—NeuroMuscular ObserVational Research, a unified data hub for neuromuscular diseases

Howell, R. R. & Zuchner, S., Mar 1 2019, In : Genetics in Medicine. 21, 3, p. 536-538 3 p.

Research output: Contribution to journalComment/debate

Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling

Undiagnosed Diseases Network, 2019, (Accepted/In press) In : Biological Psychiatry.

Research output: Contribution to journalArticle

6 Scopus citations

POLG mutations presenting as Charcot-Marie-Tooth disease

Phillips, J., Courel, S., Rebelo, A. P., Bis-Brewer, D. M., Bardakjian, T., Dankwa, L., Hamedani, A. G., Züchner, S. & Scherer, S. S., Jun 2019, In : Journal of the Peripheral Nervous System. 24, 2, p. 213-218 6 p.

Research output: Contribution to journalArticle

2 Scopus citations

Replication studies of MIR149 association in Charcot–Marie–Tooth disease type 1A in a European population

the Inherited Neuropathy Consortium, Feb 1 2019, In : Neuromuscular Disorders. 29, 2, p. 160-162 3 p.

Research output: Contribution to journalLetter

Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia

Farazi Fard, M. A., Rebelo, A. P., Buglo, E., Nemati, H., Dastsooz, H., Gehweiler, I., Reich, S., Reichbauer, J., Quintáns, B., Ordóñez-Ugalde, A., Cortese, A., Courel, S., Abreu, L., Powell, E., Danzi, M., Martuscelli, N. B., Bis-Brewer, D. M., Tao, F., Zarei, F., Habibzadeh, P. & 20 others, Yavarian, M., Modarresi, F., Silawi, M., Tabatabaei, Z., Yousefi, M., Farpour, H. R., Kessler, C., Mangold, E., Kobeleva, X., Mueller, A. J., Haack, T. B., Tarnopolsky, M., Gan-Or, Z., Rouleau, G. A., Synofzik, M., Sobrido, M. J., Jordanova, A., Schüle, R., Zuchner, S. & Faghihi, M. A., Apr 4 2019, In : American journal of human genetics. 104, 4, p. 767-773 7 p.

Research output: Contribution to journalArticle

8 Scopus citations

Variation in SIPA1L2 is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A

for the Inherited Neuropathy Consortium, Mar 2019, In : Annals of neurology. 85, 3, p. 316-330 15 p.

Research output: Contribution to journalArticle

6 Scopus citations

VarSight: Prioritizing clinically reported variants with binary classification algorithms

Holt, J. M., Wilk, B., Birch, C. L., Brown, D. M., Gajapathy, M., Moss, A. C., Sosonkina, N., Wilk, M. A., Anderson, J. A., Harris, J. M., Kelly, J. M., Shaterferdosian, F., Uno-Antonison, A. E., Weborg, A., Acosta, M. T., Adam, M., Adams, D. R., Agrawal, P. B., Alejandro, M. E., Allard, P. & 259 others, Alvey, J., Amendola, L., Andrews, A., Ashley, E. A., Azamian, M. S., Bacino, C. A., Bademci, G., Baker, E., Balasubramanyam, A., Baldridge, D., Bale, J., Bamshad, M., Barbouth, D., Batzli, G. F., Bayrak-Toydemir, P., Beck, A., Beggs, A. H., Bejerano, G., Bellen, H. J., Bennet, J., Berg-Rood, B., Bernier, R., Bernstein, J. A., Berry, G. T., Bican, A., Bivona, S., Blue, E., Bohnsack, J., Bonnenmann, C., Bonner, D., Botto, L., Briere, L. C., Brokamp, E., Burke, E. A., Burrage, L. C., Butte, M. J., Byers, P., Carey, J., Carrasquillo, O., Chang, T. C. P., Chanprasert, S., Chao, H. T., Clark, G. D., Coakley, T. R., Cobban, L. A., Cogan, J. D., Cole, F. S., Colley, H. A., Cooper, C. M., Cope, H., Craigen, W. J., Cunningham, M., D'Souza, P., Dai, H., Dasari, S., Davids, M., Dayal, J. G., Dell'Angelica, E. C., Dhar, S. U., Dipple, K., Doherty, D., Dorrani, N., Douine, E. D., Draper, D. D., Duncan, L., Earl, D., Eckstein, D. J., Emrick, L. T., Eng, C. M., Esteves, C., Estwick, T., Fernandez, L., Ferreira, C., Fieg, E. L., Fisher, P. G., Fogel, B. L., Forghani, I., Fresard, L., Gahl, W. A., Glass, I., Godfrey, R. A., Golden-Grant, K., Goldman, A. M., Goldstein, D. B., Grajewski, A., Groden, C. A., Gropman, A. L., Hahn, S., Hamid, R., Hanchard, N. A., Hayes, N., High, F., Hing, A., Hisama, F. M., Holm, I. A., Hom, J., Horike-Pyne, M., Huang, A., Huang, Y., Isasi, R., Jamal, F., Jarvik, G. P., Jarvik, J., Jayadev, S., Jiang, Y. H., Johnston, J. M., Karaviti, L., Kelley, E. G., Kiley, D., Kohane, I. S., Kohler, J. N., Krakow, D., Krasnewich, D. M., Korrick, S., Koziura, M., Krier, J. B., Lalani, S. R., Lam, B., Lam, C., Lanpher, B. C., Lanza, I. R., Lau, C. C., Leblanc, K., Lee, B. H., Lee, H., Levitt, R., Lewis, R. A., Lincoln, S. A., Liu, P., Liu, X. Z., Longo, N., Loo, S. K., Loscalzo, J., Maas, R. L., Macnamara, E. F., MacRae, C. A., Maduro, V. V., Majcherska, M. M., Malicdan, M. C. V., Mamounas, L. A., Manolio, T. A., Mao, R., Maravilla, K., Markello, T. C., Marom, R., Marth, G., Martin, B. A., Martin, M. G., Martínez-Agosto, J. A., Marwaha, S., McCauley, J., McConkie-Rosell, A., McCormack, C. E., McCray, A. T., Mefford, H., Merritt, J. L., Might, M., Mirzaa, G., Morava-Kozicz, E., Moretti, P. M., Morimoto, M., Mulvihill, J. J., Murdock, D. R., Nath, A., Nelson, S. F., Newman, J. H., Nicholas, S. K., Nickerson, D., Novacic, D., Oglesbee, D., Orengo, J. P., Pace, L., Pak, S., Pallais, J. C., Palmer, C. G. S., Papp, J. C., Parker, N. H., Phillips, J. A., Posey, J. E., Postlethwait, J. H., Potocki, L., Pusey, B. N., Quinlan, A., Raskind, W., Raja, A. N., Renteria, G., Reuter, C. M., Rives, L., Robertson, A. K., Rodan, L. H., Rosenfeld, J. A., Rowley, R. K., Ruzhnikov, M., Sacco, R., Sampson, J. B., Samson, S. L., Saporta, M., Scott, C. R., Schaechter, J., Schedl, T., Schoch, K., Scott, D. A., Shakachite, L., Sharma, P., Shashi, V., Shin, J., Signer, R., Sillari, C. H., Silverman, E. K., Sinsheimer, J. S., Sisco, K., Smith, K. S., Solnica-Krezel, L., Spillmann, R. C., Stoler, J. M., Stong, N., Sullivan, J. A., Sun, A., Sutton, S., Sweetser, D. A., Sybert, V., Tabor, H. K., Tamburro, C. P., Tan, Q. K. G., Tekin, M., Telischi, F., Thorson, W., Tifft, C. J., Toro, C., Tran, A. A., Urv, T. K., Velinder, M., Viskochil, D., Vogel, T. P., Wahl, C. E., Wallace, S., Walley, N. M., Walsh, C. A., Walker, M., Wambach, J., Wan, J., Wang, L. K., Wangler, M. F., Ward, P. A., Wegner, D., Wener, M., Westerfield, M., Wheeler, M. T., Wise, A. L., Wolfe, L. A., Woods, J. D., Yamamoto, S., Yang, J., Yoon, A. J., Yu, G., Zastrow, D. B., Zhao, C., Zuchner, S. & Worthey, E. A., Oct 15 2019, In : BMC Bioinformatics. 20, 1, 496.

Research output: Contribution to journalArticle

Open Access
3 Scopus citations
2018

A mutation in the heptad repeat 2 domain of MFN2 in a large CMT2A family

Dankwa, L., Richardson, J., Motley, W. W., Zuchner, S. L. & Scherer, S. S., Jan 1 2018, (Accepted/In press) In : Journal of the Peripheral Nervous System.

Research output: Contribution to journalArticle

2 Scopus citations

Beyond ALS and FTD: the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypes

Wilke, C., Baets, J., De Bleecker, J. L., Deconinck, T., Biskup, S., Hayer, S. N., Züchner, S., Schüle, R., De Jonghe, P. & Synofzik, M., Feb 2018, In : Neurobiology of aging. 62, p. 244.e9-244.e13

Research output: Contribution to journalArticle

10 Scopus citations

Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function

Mendoza-Ferreira, N., Coutelier, M., Janzen, E., Hosseinibarkooie, S., Löhr, H., Schneider, S., Milbradt, J., Karakaya, M., Riessland, M., Pichlo, C., Torres-Benito, L., Singleton, A., Zuchner, S., Brice, A., Durr, A., Hammerschmidt, M., Stevanin, G. & Wirth, B., Feb 1 2018, In : Neurology: Genetics. 4, 1, e209.

Research output: Contribution to journalArticle

10 Scopus citations

De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel function

Synofzik, M., Helbig, K. L., Harmuth, F., Deconinck, T., Tanpaiboon, P., Sun, B., Guo, W., Wang, R., Palmaer, E., Tang, S., Schaefer, G. B., Gburek-Augustat, J., Züchner, S., Krägeloh-Mann, I., Baets, J., de Jonghe, P., Bauer, P., Chen, S. R. W., Schöls, L. & Schüle, R., Nov 1 2018, In : European Journal of Human Genetics. 26, 11, p. 1623-1634 12 p.

Research output: Contribution to journalArticle

12 Scopus citations

Erratum: SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency (Brain (2018) 141 (662-672) DOI: 10.1093/brain/awx369)

Rebelo, A., Dimah, S., Pereira, C., Farooq, A., Huff, T., Abreu, L., Moraes, C., Mnatsakanova, D., Mathews, K., Yang, H., Schon, E., Zuchner, S. & Shy, M., Apr 1 2018, In : Brain. 141, 4, e32.

Research output: Contribution to journalComment/debate

GDAP2 mutations implicate susceptibility to cellular stress in a new form of cerebellar ataxia

Eidhof, I., Baets, J., Kamsteeg, E. J., Deconinck, T., Van Ninhuijs, L., Martin, J. J., Schüle, R., Züchner, S., De Jonghe, P., Schenck, A. & Van De Warrenburg, B. P., Sep 1 2018, In : Brain. 141, 9, p. 2592-2604 13 p.

Research output: Contribution to journalArticle

2 Scopus citations

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

ITALSGEN Consortium, Genomic Translation for ALS Care (GTAC) Consortium, ALS Sequencing Consortium, NYGC ALS Consortium, Answer ALS Foundation, Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium, SLAGEN Consortium, French ALS Consortium & Project MinE ALS Sequencing Consortium, Mar 21 2018, In : Neuron. 97, 6, p. 1268-1283.e6

Research output: Contribution to journalArticle

102 Scopus citations

Identification of a new SYT2 variant validates an unusual distal motor neuropathy phenotype

Montes-Chinea, N. I., Guan, Z., Coutts, M., Vidal, C., Courel, S., Rebelo, A. P., Abreu, L., Zuchner, S., Troy Littleton, J. & Saporta, M. A., Dec 1 2018, In : Neurology: Genetics. 4, 6, e282.

Research output: Contribution to journalArticle

1 Scopus citations

Identification of compound heterozygous variants in OPTN in an ALS-FTD patient from the CReATe consortium: a case report

Pottier, C., Rampersaud, E., Baker, M., Wu, G., Wuu, J., McCauley, J. L., Zuchner, S., Schule, R., Bermudez, C., Hussain, S., Cooley, A., Wallace, M., Zhang, J., Taylor, J. P., Benatar, M. & Rademakers, R., Mar 20 2018, (Accepted/In press) In : Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. p. 1-3 3 p.

Research output: Contribution to journalArticle

2 Scopus citations

Insights into the genotype-phenotype correlation and molecular function of SLC25A46

Abrams, A. J., Fontanesi, F., Tan, N. B. L., Buglo, E., Campeanu, I. J., Rebelo, A. P., Kornberg, A. J., Phelan, D. G., Stark, Z. & Zuchner, S. L., Jan 1 2018, (Accepted/In press) In : Human Mutation.

Research output: Contribution to journalArticle

7 Scopus citations

MFN2-associated lipomatosis: Clinical spectrum and impact on adipose tissue

Capel, E., Vatier, C., Cervera, P., Stojkovic, T., Disse, E., Cottereau, A. S., Auclair, M., Verpont, M. C., Mosbah, H., Gourdy, P., Barraud, S., Miquel, A., Züchner, S., Bonnefond, A., Froguel, P., Christin-Maitre, S., Delemer, B., Fève, B., Laville, M., Robert, J. & 4 others, Tenenbaum, F., Lascols, O., Vigouroux, C. & Jéru, I., Nov 1 2018, In : Journal of Clinical Lipidology. 12, 6, p. 1420-1435 16 p.

Research output: Contribution to journalArticle

7 Scopus citations

Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2

Lassuthova, P., Rebelo, A. P., Ravenscroft, G., Lamont, P. J., Davis, M. R., Manganelli, F., Feely, S. M., Bacon, C., Brožková, D. Š., Haberlova, J., Mazanec, R., Tao, F., Saghira, C., Abreu, L., Courel, S., Powell, E., Buglo, E., Bis, D. M., Baxter, M. F., Ong, R. W. & 14 others, Marns, L., Lee, Y. C., Bai, Y., Isom, D. G., Barro-Soria, R., Chung, K. W., Scherer, S. S., Larsson, H. P., Laing, N. G., Choi, B. O., Seeman, P., Shy, M. E., Santoro, L. & Zuchner, S., Mar 1 2018, In : American journal of human genetics. 102, 3, p. 505-514 10 p.

Research output: Contribution to journalArticle

14 Scopus citations

Mutations in BAG3 cause adult-onset Charcot-Marie-Tooth disease

Shy, M., Rebelo, A. P., Feely, S. M., Abreu, L. A., Tao, F., Swenson, A., Bacon, C. & Zuchner, S. L., Mar 1 2018, In : Journal of Neurology, Neurosurgery and Psychiatry. 89, 3, p. 313-316 4 p.

Research output: Contribution to journalLetter

7 Scopus citations

Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks

Meister-Broekema, M., Freilich, R., Jagadeesan, C., Rauch, J. N., Bengoechea, R., Motley, W. W., Kuiper, E. F. E., Minoia, M., Furtado, G. V., van Waarde, M. A. W. H., Bird, S. J., Rebelo, A., Zuchner, S., Pytel, P., Scherer, S. S., Morelli, F. F., Carra, S., Weihl, C. C., Bergink, S., Gestwicki, J. E. & 1 others, Kampinga, H. H., Dec 1 2018, In : Nature communications. 9, 1, 5342.

Research output: Contribution to journalArticle

11 Scopus citations