Research output per year
Research output per year
- 1 - 50 out of 148 results
Search results
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2024
An adult with KCNA2-related epilepsy and ataxia
DeKorver, N. W., Zhao, W., Butler, M. R., Di Luca, D. G., Gurnett, C. & Nascimento, F., Apr 2024, In: Epileptic Disorders. 26, 2, p. 264-266 3 p.Research output: Contribution to journal › Article › peer-review
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Assessment of COVID-19 Messaging Strategies to Increase Testing for Students With Intellectual and Developmental Disabilities
Walsh, T. J., Kalb, L. G., Gemmell, M., Liu, J., Caburnay, C. A., Gurnett, C. A. & Newland, J. G., Jun 2024, In: Journal of School Health. 94, 6, p. 551-561 11 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis
Yu, H., Khanshour, A. M., Ushiki, A., Otomo, N., Koike, Y., Einarsdottir, E., Fan, Y., Antunes, L., Kidane, Y. H., Cornelia, R., Sheng, R. R., Zhang, Y., Pei, J., Grishin, N. V., Evers, B. M., Cheung, J. P. Y., Herring, J. A., Terao, C., Song, Y. Q. & Gurnett, C. A. & 5 others, , 2024, In: eLife. 13, RP89762.Research output: Contribution to journal › Article › peer-review
Open Access -
Clinical variants paired with phenotype: A rich resource for brain gene curation
Brain Gene Registry Consortium, Mar 2024, In: Genetics in Medicine. 26, 3, 101035.Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations -
Exome sequencing of 1190 non-syndromic clubfoot cases reveals HOXD12 as a novel disease gene
Charng, W. L., Nikolov, M., Shrestha, I., Seeley, M. A., Josyula, N. S., Justice, A. E., Dobbs, M. B. & Gurnett, C. A., Jun 20 2024, In: Journal of Medical Genetics. 61, 7, p. 699-706 8 p.Research output: Contribution to journal › Article › peer-review
Open Access -
The Brain Gene Registry: a data snapshot
Baldridge, D., Kaster, L., Sancimino, C., Srivastava, S., Molholm, S., Gupta, A., Oh, I., Lanzotti, V., Grewal, D., Riggs, E. R., Savatt, J. M., Hauck, R., Sveden, A., Constantino, J. N., Piven, J., Gurnett, C. A., Chopra, M., Hazlett, H. & Payne, P. R. O., Dec 2024, In: Journal of neurodevelopmental disorders. 16, 1, 17.Research output: Contribution to journal › Article › peer-review
Open Access -
2023
Building School-Academic Partnerships to Implement COVID-19 Testing in Underserved Populations
Goldman, J. L., Kalu, I. C., Schuster, J. E., Erickson, T., Mast, D. K., Zimmerman, K., Benjamin, D. K., Kalb, L. G., Gurnett, C., Newland, J. G., Sherby, M., Godambe, M., Shinde, N., Watterson, T., Walsh, T., Foxe, J., Zand, M., Dewhurst, S., Coller, R. & DeMuri, G. P. & 22 others, , Jul 2023, In: Pediatrics. 152, e2022060352C.Research output: Contribution to journal › Article › peer-review
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Caregiver perspectives on the continued impact of the COVID-19 pandemic on children with intellectual/developmental disabilities
Northrup, R. A., Jones, E., Singh, V., Holingue, C., Meck, M., Gurnett, C. A., van Stone, M. & Kalb, L. G., Aug 7 2023, In: Frontiers in Pediatrics. 11, 1196275.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
Clusters of SARS-CoV-2 Infection Across Six Schools for Students with Intellectual and Developmental Disabilities
Gemmell, M., Walsh, T., Sherby, M., Imbeah, A., Bono, K., Baldenweck, M., Gurnett, C. & Newland, J. G., Sep 2023, In: Infectious Diseases and Therapy. 12, 9, p. 2289-2294 6 p.Research output: Contribution to journal › Article › peer-review
Open Access -
COL11A2 as a candidate gene for vertebral malformations and congenital scoliosis
Rebello, D., Wohler, E., Erfani, V., Li, G., Aguilera, A. N., Santiago-Cornier, A., Zhao, S., Hwang, S. W., Steiner, R. D., Zhang, T. J., Gurnett, C. A., Raggio, C., Wu, N., Sobreira, N., Giampietro, P. F. & Ciruna, B., Oct 1 2023, In: Human molecular genetics. 32, 19, p. 2913-2928 16 p.Research output: Contribution to journal › Article › peer-review
3 Scopus citations -
Common Data Element Collection in Underserved School Communities: Challenges and Recommendations
Uthappa, D. M., Mann, T. K., Goldman, J. L., Schuster, J. E., Newland, J. G., Anderson, W. B., Dozier, A., Inkelas, M., Foxe, J. J., Gwynn, L., Gurnett, C. A., McDaniels-Davidson, C., Walsh, T., Watterson, T., Holden-Wiltse, J., Potts, J. M., D’Agostino, E. M., Zandi, K., Corbett, A. & Spallina, S. & 16 others, , Jul 2023, In: Pediatrics. 152, e2022060352N.Research output: Contribution to journal › Article › peer-review
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Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development
Focal Cortical Dysplasia Neurogenetics Consortium, Brain Somatic Mosaicism Network, Gurnett, C. A., Smyth, M. D., Gurnett, C. A. & Smyth, M. D., Feb 1 2023, In: Nature Genetics. 55, 2, p. 209-220 12 p.Research output: Contribution to journal › Article › peer-review
Open Access31 Scopus citations -
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology
Oppermann, H., Marcos-Grañeda, E., Weiss, L. A., Gurnett, C. A., Jelsig, A. M., Vineke, S. H., Isidor, B., Mercier, S., Magnussen, K., Zacher, P., Hashim, M., Pagnamenta, A. T., Race, S., Srivastava, S., Frazier, Z., Maiwald, R., Pergande, M., Milani, D., Rinelli, M. & Levy, J. & 35 others, , Nov 2023, In: European Journal of Human Genetics. 31, 11, p. 1251-1260 10 p.Research output: Contribution to journal › Article › peer-review
Open Access4 Scopus citations -
Quantitative determination of SLC2A1 variant functional effects in GLUT1 deficiency syndrome
Tayebi, N., Leon-Ricardo, B., McCall, K., Mehinovic, E., Engelstad, K., Huynh, V., Turner, T. N., Weisenberg, J., Thio, L. L., Hruz, P., Williams, R. S. B., De Vivo, D. C., Petit, V., Haller, G. & Gurnett, C. A., May 2023, In: Annals of Clinical and Translational Neurology. 10, 5, p. 787-801 15 p.Research output: Contribution to journal › Article › peer-review
Open Access4 Scopus citations -
Recommendations for SARS-CoV-2 Testing in Children With Disabilities and Medical Complexity
Gemmell, M., Sherby, M. R., Walsh, T. J., Kalb, L. G., Johnson, S. B., Coller, R. J., DeMuri, G. P., Nuthals, E., McBride, J., Newland, J. G. & Gurnett, C. A., Jul 1 2023, In: Pediatrics. 152, e2022060352G.Research output: Contribution to journal › Article › peer-review
2 Scopus citations -
2022
A pathogenic mechanism associated with myopathies and structural birth defects involves TPM2-directed myogenesis
McAdow, J., Yang, S., Ou, T., Huang, G., Dobbs, M. B., Gurnett, C. A., Greenberg, M. J. & Johnson, A. N., Jun 22 2022, In: JCI Insight. 7, 12, e152466.Research output: Contribution to journal › Article › peer-review
Open Access5 Scopus citations -
Diagnostic yield of exome sequencing in congenital vertical talus
Tayebi, N., Charng, W. L., Dickson, P. I., Dobbs, M. B. & Gurnett, C. A., Jun 2022, In: European Journal of Medical Genetics. 65, 6, 104514.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
Distinct epilepsy phenotypes and response to drugs in KCNA1 gain- and loss-of function variants
Miceli, F., Guerrini, R., Nappi, M., Soldovieri, M. V., Cellini, E., Gurnett, C. A., Parmeggiani, L., Mei, D. & Taglialatela, M., Jan 2022, In: Epilepsia. 63, 1, p. e7-e14Research output: Contribution to journal › Article › peer-review
Open Access23 Scopus citations -
Diverse monogenic subforms of human spermatogenic failure
Nagirnaja, L., Lopes, A. M., Charng, W. L., Miller, B., Stakaitis, R., Golubickaite, I., Stendahl, A., Luan, T., Friedrich, C., Mahyari, E., Fadial, E., Kasak, L., Vigh-Conrad, K., Oud, M. S., Xavier, M. J., Cheers, S. R., James, E. R., Guo, J., Jenkins, T. G. & Riera-Escamilla, A. & 29 others, , Dec 2022, In: Nature communications. 13, 1, 7953.Research output: Contribution to journal › Article › peer-review
Open Access25 Scopus citations -
Effect of Clonal Hematopoiesis on Cardiovascular Disease in People Living with HIV
Wiley, B., Parsons, T. M., Burkart, S., Young, A. L., Erlandson, K. M., Tassiopoulos, K. K., Wu, K., Gurnett, C., Presti, R. M., Bolton, K. L. & Challen, G. A., Oct 2022, In: Experimental Hematology. 114, p. 18-21 4 p.Research output: Contribution to journal › Article › peer-review
Open Access9 Scopus citations -
Germline mosaicism of a missense variant in KCNC2 in a multiplex family with autism and epilepsy characterized by long-read sequencing
Mehinovic, E., Gray, T., Campbell, M., Ekholm, J., Wenger, A., Rowell, W., Grudo, A., Grimwood, J., Korlach, J., Gurnett, C., Constantino, J. N. & Turner, T. N., Jul 2022, In: American Journal of Medical Genetics, Part A. 188, 7, p. 2071-2081 11 p.Research output: Contribution to journal › Article › peer-review
Open Access6 Scopus citations -
Hereditary alpha-tryptasemia modifies clinical phenotypes among individuals with congenital hypermobility disorders
Vazquez, M., Chovanec, J., Kim, J., DiMaggio, T., Milner, J. D., Francomano, C. A., Gurnett, C. A., Ritelli, M., Colombi, M. & Lyons, J. J., Apr 14 2022, In: Human Genetics and Genomics Advances. 3, 2, 100094.Research output: Contribution to journal › Article › peer-review
Open Access5 Scopus citations -
Supporting COVID-19 School Safety for Children With Disabilities and Medical Complexity
Sherby, M. R., Kalb, L. G., Coller, R. J., DeMuri, G. P., Butteris, S., Foxe, J. J., Zand, M. S., Freedman, E. G., Dewhurst, S., Newland, J. G. & Gurnett, C. A., Feb 1 2022, In: Pediatrics. 149, e2021054268H.Research output: Contribution to journal › Article › peer-review
15 Scopus citations -
Understanding educators’ perspectives and experiences of COVID-19 in schools serving children with intellectual/developmental disabilities
Jones, E. F., Singh, V., Holingue, C., Errichetti, C. L., Myers, L., Sherby, M. R., Gurnett, C., Newland, J. & Kalb, L., Oct 31 2022, In: Frontiers in Education. 7, 949430.Research output: Contribution to journal › Article › peer-review
Open Access -
Whole-exome analysis of adolescents with low VWF and heavy menstrual bleeding identifies novel genetic associations
Sadler, B., Minard, C. G., Haller, G., Gurnett, C. A., O'Brien, S. H., Wheeler, A., Jain, S., Sharma, M., Zia, A., Kulkarni, R., Mullins, E., Ragni, M. V., Sidonio, R., Dietrich, J. E., Kouides, P. A., Di Paola, J. & Srivaths, L., Jan 25 2022, In: Blood Advances. 6, 2, p. 420-428 9 p.Research output: Contribution to journal › Article › peer-review
Open Access4 Scopus citations -
Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion
Quiggle, A., Charng, W. L., Antunes, L., Nikolov, M., Bledsoe, X., Hecht, J. T., Dobbs, M. B. & Gurnett, C. A., Feb 1 2022, In: Clinical orthopaedics and related research. 480, 2, p. 421-430 10 p.Research output: Contribution to journal › Article › peer-review
Open Access5 Scopus citations -
2021
A decade in review after idiopathic scoliosis was first called a complex trait—a tribe to the late Dr. Yves Cotrel for his support in studies of etiology of scoliosis
Tang, N. L. S., Dobbs, M. B., Gurnett, C. A., Qiu, Y., Lam, T. P., Cheng, J. C. Y. & Hadley-Miller, N., Jul 2021, In: Genes. 12, 7, 1033.Research output: Contribution to journal › Review article › peer-review
Open Access7 Scopus citations -
Cellular and plasma proteomic determinants of COVID-19 and non-COVID-19 pulmonary diseases relative to healthy aging
Arthur, L., Esaulova, E., Mogilenko, D. A., Tsurinov, P., Burdess, S., Laha, A., Presti, R., Goetz, B., Watson, M. A., Goss, C. W., Gurnett, C. A., Mudd, P. A., Beers, C., O’Halloran, J. A. & Artyomov, M. N., Jun 2021, In: Nature Aging. 1, 6, p. 535-549 15 p.Research output: Contribution to journal › Article › peer-review
Open Access23 Scopus citations -
Erratum: Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001))
Sadler, B., Wilborn, J., Antunes, L., Kuensting, T., Hale, A. T., Gannon, S. R., McCall, K., Cruchaga, C., Harms, M., Voisin, N., Reymond, A., Cappuccio, G., Brunetti-Pierri, N., Tartaglia, M., Niceta, M., Leoni, C., Zampino, G., Ashley-Koch, A., Urbizu, A. & Garrett, M. E. & 11 others, , Feb 4 2021, In: American journal of human genetics. 108, 2, p. 368 1 p.Research output: Contribution to journal › Comment/debate
Open Access3 Scopus citations -
Erratum: Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001))
Sadler, B., Wilborn, J., Antunes, L., Kuensting, T., Hale, A. T., Gannon, S. R., McCall, K., Cruchaga, C., Harms, M., Voisin, N., Reymond, A., Cappuccio, G., Brunetti-Pierri, N., Tartaglia, M., Niceta, M., Leoni, C., Zampino, G., Ashley-Koch, A., Urbizu, A. & Garrett, M. E. & 11 others, , Mar 4 2021, In: American journal of human genetics. 108, 3, p. 530-531 2 p.Research output: Contribution to journal › Comment/debate
Open Access3 Scopus citations -
Genetic counseling as preventive intervention: toward individual specification of transgenerational autism risk
Marrus, N., Turner, T. N., Forsen, E., Bolster, D., Marvin, A., Whitehouse, A., Klinger, L., Gurnett, C. A. & Constantino, J. N., Dec 2021, In: Journal of neurodevelopmental disorders. 13, 1, 39.Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations -
Jean Holowach Thurston
Gurnett, C. A., Zempel, J. & Noetzel, M. J., Jan 1 2021, Child Neurology: Its Origins, Founders, Growth and Evolution. Elsevier, p. 766-768 3 p.Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review
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Models of distal arthrogryposis and lethal congenital contracture syndrome
Whittle, J., Johnson, A., Dobbs, M. B. & Gurnett, C. A., Jun 2021, In: Genes. 12, 6, 943.Research output: Contribution to journal › Article › peer-review
Open Access9 Scopus citations -
Mutations in KIF7 implicated in idiopathic scoliosis in humans and axial curvatures in zebrafish
Terhune, E. A., Cuevas, M. T., Monley, A. M., Wethey, C. I., Chen, X., Cattell, M. V., Bayrak, M. N., Bland, M. R., Sutphin, B., Trahan, G. D., Taylor, M. R. G., Niswander, L. A., Jones, K. L., Baschal, E. E., Antunes, L., Dobbs, M., Gurnett, C., Appel, B., Gray, R. & Hadley Miller, N., Apr 2021, In: Human mutation. 42, 4, p. 392-407 16 p.Research output: Contribution to journal › Article › peer-review
Open Access18 Scopus citations -
Rare and de novo coding variants in chromodomain genes in Chiari I malformation
Sadler, B., Wilborn, J., Antunes, L., Kuensting, T., Hale, A. T., Gannon, S. R., McCall, K., Cruchaga, C., Harms, M., Voisin, N., Reymond, A., Cappuccio, G., Burnetti-Pierri, N., Tartaglia, M., Niceta, M., Leoni, C., Zampino, G., Ashley-Koch, A., Urbizu, A. & Garrett, M. E. & 11 others, , Jan 7 2021, In: American journal of human genetics. 108, 1, p. 100-114 15 p.Research output: Contribution to journal › Article › peer-review
Open Access14 Scopus citations -
SARS-CoV-2 screening testing in schools for children with intellectual and developmental disabilities
for the COMPASS-T Study Group, Dec 2021, In: Journal of neurodevelopmental disorders. 13, 1, 31.Research output: Contribution to journal › Article › peer-review
Open Access11 Scopus citations -
Sex- and Mutation-Specific p53 Gain-of-Function Activity in Gliomagenesis
Rockwell, N. C., Yang, W., Warrington, N. M., Staller, M. V., Griffith, M., Griffith, O. L., Gurnett, C. A., Cohen, B. A., Baldridge, D. & Rubin, J. B., Dec 2021, In: Cancer research communications. 1, 3, p. 148-163 16 p.Research output: Contribution to journal › Article › peer-review
Open Access6 Scopus citations -
2020
ATRAID regulates the action of nitrogen-containing bisphosphonates on bone
Surface, L. E., Burrow, D. T., Li, J., Park, J., Kumar, S., Lyu, C., Song, N., Yu, Z., Rajagopal, A., Bae, Y., Lee, B. H., Mumm, S., Gu, C. C., Baker, J. C., Mohseni, M., Sum, M., Huskey, M., Duan, S., Bijanki, V. N. & Civitelli, R. & 18 others, , May 20 2020, In: Science translational medicine. 12, 544, eaav9166.Research output: Contribution to journal › Article › peer-review
Open Access13 Scopus citations -
Comprehensive In Vivo Interrogation Reveals Phenotypic Impact of Human Enhancer Variants
Kvon, E. Z., Zhu, Y., Kelman, G., Novak, C. S., Plajzer-Frick, I., Kato, M., Garvin, T. H., Pham, Q., Harrington, A. N., Hunter, R. D., Godoy, J., Meky, E. M., Akiyama, J. A., Afzal, V., Tran, S., Escande, F., Gilbert-Dussardier, B., Jean-Marçais, N., Hudaiberdiev, S. & Ovcharenko, I. & 7 others, , Mar 19 2020, In: Cell. 180, 6, p. 1262-1271.e15Research output: Contribution to journal › Article › peer-review
Open Access82 Scopus citations -
Genetic association and characterization of FSTL5 in isolated clubfoot
Khanshour, A. M., Kidane, Y. H., Kozlitina, J., Cornelia, R., Rafipay, A., De Mello, V., Weston, M., Paria, N., Khalid, A., Hecht, J. T., Dobbs, M. B., Richards, B. S., Vargesson, N., Hamra, F. K., Wilson, M., Wise, C., Gurnett, C. A. & Rios, J. J., Nov 15 2020, In: Human molecular genetics. 29, 22, p. 3717-3728 12 p.Research output: Contribution to journal › Article › peer-review
Open Access6 Scopus citations -
Human iPSC-Derived Neuronal Cells From CTBP1-Mutated Patients Reveal Altered Expression of Neurodevelopmental Gene Networks
Vijayalingam, S., Ezekiel, U. R., Xu, F., Subramanian, T., Geerling, E., Hoelscher, B., San, K. K., Ganapathy, A., Pemberton, K., Tycksen, E., Pinto, A. K., Brien, J. D., Beck, D. B., Chung, W. K., Gurnett, C. A. & Chinnadurai, G., Oct 27 2020, In: Frontiers in Neuroscience. 14, 562292.Research output: Contribution to journal › Article › peer-review
Open Access7 Scopus citations -
MYH3-associated distal arthrogryposis zebrafish model is normalized with para-aminoblebbistatin
Whittle, J., Antunes, L., Harris, M., Upshaw, Z., Sepich, D. S., Johnson, A. N., Mokalled, M., Solnica-Krezel, L., Dobbs, M. B. & Gurnett, C. A., Nov 6 2020, In: EMBO Molecular Medicine. 12, 11, e12356.Research output: Contribution to journal › Article › peer-review
Open Access16 Scopus citations -
Obex position is associated with syringomyelia and use of posterior fossa decompression among patients with Chiari I malformation
Haller, G., Sadler, B., Kuensting, T., Lakshman, N., Greenberg, J. K., Strahle, J. M., Park, T. S., Dobbs, M. B., Gurnett, C. A. & Limbrick, D. D., Jul 2020, In: Journal of Neurosurgery: Pediatrics. 26, 1, p. 45-52 8 p.Research output: Contribution to journal › Article › peer-review
Open Access14 Scopus citations -
Prevalence and Impact of Underlying Diagnosis and Comorbidities on Chiari 1 Malformation
Sadler, B., Kuensting, T., Strahle, J., Park, T. S., Smyth, M., Limbrick, D. D., Dobbs, M. B., Haller, G. & Gurnett, C. A., May 2020, In: Pediatric Neurology. 106, p. 32-37 6 p.Research output: Contribution to journal › Article › peer-review
Open Access27 Scopus citations -
Rare and de novo duplications containing SHOX in clubfoot
Sadler, B., Haller, G., Antunes, L., Nikolov, M., Amarillo, I., Coe, B., Dobbs, M. B. & Gurnett, C. A., Dec 1 2020, In: Journal of Medical Genetics. 57, 12, p. 851-857 7 p.Research output: Contribution to journal › Article › peer-review
Open Access10 Scopus citations -
The cartilage matrisome in adolescent idiopathic scoliosis
Wise, C. A., Sepich, D., Ushiki, A., Khanshour, A. M., Kidane, Y. H., Makki, N., Gurnett, C. A., Gray, R. S., Rios, J. J., Ahituv, N. & Solnica-Krezel, L., Dec 1 2020, In: Bone Research. 8, 1, 13.Research output: Contribution to journal › Review article › peer-review
Open Access28 Scopus citations -
2019
Distal chromosome 16p11.2 duplications containing SH2B1 in patients with scoliosis
Sadler, B., Haller, G., Antunes, L., Bledsoe, X., Morcuende, J., Giampietro, P., Raggio, C., Miller, N., Kidane, Y., Wise, C. A., Amarillo, I., Walton, N., Seeley, M., Johnson, D., Jenkins, C., Jenkins, T., Oetjens, M., Tong, R. S., Druley, T. E. & Dobbs, M. B. & 1 others, , Jul 1 2019, In: Journal of Medical Genetics. 56, 7, p. 427-433 7 p.Research output: Contribution to journal › Article › peer-review
Open Access14 Scopus citations -
MET mutation causes muscular dysplasia and arthrogryposis
Zhou, H., Lian, C., Wang, T., Yang, X., Xu, C., Su, D., Zheng, S., Huang, X., Liao, Z., Zhou, T., Qiu, X., Chen, Y., Gao, B., Li, Y., Wang, X., You, G., Fu, Q., Gurnett, C., Huang, D. & Su, P., Mar 2019, In: EMBO Molecular Medicine. 11, 3, e9709.Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations -
The genetics of isolated and syndromic clubfoot
Sadler, B., Gurnett, C. A. & Dobbs, M. B., 2019, In: Journal of Children's Orthopaedics. 13, 3, p. 238-244 7 p.Research output: Contribution to journal › Review article › peer-review
Open Access29 Scopus citations -
2018
A missense variant in SLC39A8 is associated with severe idiopathic scoliosis
Haller, G., McCall, K., Jenkitkasemwong, S., Sadler, B., Antunes, L., Nikolov, M., Whittle, J., Upshaw, Z., Shin, J., Baschal, E., Cruchaga, C., Harms, M., Raggio, C., Morcuende, J. A., Giampietro, P., Miller, N. H., Wise, C., Gray, R. S., Solnica-Krezel, L. & Knutson, M. & 2 others, , Dec 1 2018, In: Nature communications. 9, 1, 4171.Research output: Contribution to journal › Article › peer-review
Open Access50 Scopus citations