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ArticlesPeer ReviewedFull Text
Amyotrophic lateral sclerosis is over-represented in two Huntington’s disease brain bank cohorts: further evidence to support genetic pleiotropy of pathogenic HTT gene expansion
Author / Creator:Hickman, Richard A. ; Dewan, Ramita ; Cortes, Etty ; Traynor, Bryan J. ; Marder, Karen ; Vonsattel, Jean-Paul
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Acta neuropathologica, 2022-01, Vol.143 (1), p.105-108
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ArticlesPeer ReviewedFull Text
Comparative clinical and genomic analysis of neurofibromatosis type 2-associated cranial and spinal meningiomas
Author / Creator:Pemov, Alexander ; Dewan, Ramita ; Hansen, Nancy F. ; Chandrasekharappa, Settara C. ; Ray-Chaudhury, Abhik ; Jones, Kristine ; Luo, Wen ; Heiss, John D. ; Mullikin, James C. ; Chittiboina, Prashant ; Stewart, Douglas R. ; Asthagiri, Ashok R.
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2020-07, Vol.10 (1), p.12563-12563, Article 12563
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ArticlesPeer ReviewedFull Text
In search of genetic factors predisposing to familial hairy cell leukemia (HCL): exome-sequencing of four multiplex HCL pedigrees
Author / Creator:Pemov, Alexander ; Pathak, Anand ; Jones, Samantha J. ; Dewan, Ramita ; Merberg, Jessica ; Karra, Sirisha ; Kim, Jung ; Arons, Evgeny ; Ravichandran, Sarangan ; Luke, Brian T. ; Suman, Shalabh ; Yeager, Meredith ; Dyer, Martin J. S. ; Lynch, Henry T. ; Greene, Mark H. ; Caporaso, Neil E. ; Kreitman, Robert J. ; Goldin, Lynn R. ; Spinelli, John J. ; Brooks-Wilson, Angela ; McMaster, Mary L. ; Stewart, Douglas R.
Publisher:London: Nature Publishing Group UK
Journal title:Leukemia, 2020-07, Vol.34 (7), p.1934-1938
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ArticlesPeer ReviewedFull Text
The Association of CD81 Polymorphisms with Alloimmunization in Sickle Cell Disease
Author / Creator:Girot, Robert ; Vukmanovic, Stanislav ; Rajagopal, Krishnamoorthy ; Maury, Jacqueline ; Lasserre, Jacqueline ; Luban, Naomi L. C. ; Dewan, Ramita ; Le Bouder, Gama P. ; Tamouza, Ryad ; Tatari-Calderone, Zohreh ; Lionnet, François
Publisher:Cairo, Egypt: Hindawi Publishing Corporation
Journal title:Journal of immunology research, 2013-01, Vol.2013 (2013), p.1-9
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ArticlesPeer ReviewedFull Text
Age-related accumulation of T cells with markers of relatively stronger autoreactivity leads to functional erosion of T cells
Author / Creator:Tatari-Calderone, Zohreh ; Stojakovic, Milica ; Dewan, Ramita ; Bouder, Gama Le ; Jankovic, Dragana ; Vukmanovic, Stanislav
Publisher:England: BioMed Central Ltd
Journal title:BMC immunology, 2012-02, Vol.13 (1), p.8-8, Article 8
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ArticlesPeer ReviewedFull Text
Plasma microRNA signature as biomarker for disease progression in frontotemporal dementia and amyotrophic lateral sclerosis
Author / Creator:Dewan, Ramita ; Traynor, Bryan J
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of neurology, neurosurgery and psychiatry, 2021-05, Vol.92 (5), p.458-458
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ArticlesPeer ReviewedFull Text
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
Author / Creator:Kolmogorov, Mikhail ; Billingsley, Kimberley J. ; Mastoras, Mira ; Meredith, Melissa ; Monlong, Jean ; Lorig-Roach, Ryan ; Asri, Mobin ; Alvarez Jerez, Pilar ; Malik, Laksh ; Dewan, Ramita ; Reed, Xylena ; Genner, Rylee M. ; Daida, Kensuke ; Behera, Sairam ; Shafin, Kishwar ; Pesout, Trevor ; Prabakaran, Jeshuwin ; Carnevali, Paolo ; Yang, Jianzhi ; Rhie, Arang ; Scholz, Sonja W. ; Traynor, Bryan J. ; Miga, Karen H. ; Jain, Miten ; Timp, Winston ; Phillippy, Adam M. ; Chaisson, Mark ; Sedlazeck, Fritz J. ; Blauwendraat, Cornelis ; Paten, Benedict
Publisher:New York: Nature Publishing Group US
Journal title:Nature methods, 2023-10, Vol.20 (10), p.1483-1492
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ArticlesPeer ReviewedFull Text
Intermediate HTT CAG repeats worsen disease severity in amyotrophic lateral sclerosis
Author / Creator:Grassano, Maurizio ; Canosa, Antonio ; Sandra D’Alfonso ; Corrado, Lucia ; Brodini, Giorgia ; Koumantakis, Emanuele ; Cugnasco, Paolo ; Manera, Umberto ; Vasta, Rosario ; Palumbo, Francesca ; Mazzini, Letizia ; Gallone, Salvatore ; Moglia, Cristina ; Dewan, Ramita ; Chia, Ruth ; Ding, Jinhui ; Dalgard, Clifton ; Gibbs, Raphael J ; Scholz, Sonja ; Calvo, Andrea ; Traynor, Bryan ; Chio, Adriano
Publisher:London: BMJ Publishing Group LTD
Journal title:Journal of neurology, neurosurgery and psychiatry, 2025-01, p.jnnp-2024-333998
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ArticlesPeer ReviewedFull Text
First insight into the somatic mutation burden of neurofibromatosis type 2-associated grade I and grade II meningiomas: a case report comprehensive genomic study of two cranial meningiomas with vastly...
Author / Creator:Dewan, Ramita ; Pemov, Alexander ; Dutra, Amalia S. ; Pak, Evgenia D. ; Edwards, Nancy A. ; Ray-Chaudhury, Abhik ; Hansen, Nancy F. ; Chandrasekharappa, Settara C. ; Mullikin, James C. ; Asthagiri, Ashok R. ; Heiss, John D. ; Stewart, Douglas R. ; Germanwala, Anand V.
Publisher:England: BioMed Central
Journal title:BMC cancer, 2017-02, Vol.17 (1), p.127-127, Article 127
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ArticlesPeer ReviewedFull Text
Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large family
Author / Creator:Pathak, Anand ; Pemov, Alexander ; McMaster, Mary L. ; Dewan, Ramita ; Ravichandran, Sarangan ; Pak, Evgenia ; Dutra, Amalia ; Lee, Hyo Jung ; Vogt, Aurelie ; Zhang, Xijun ; Yeager, Meredith ; Anderson, Stacie ; Kirby, Martha ; Caporaso, Neil ; Greene, Mark H. ; Goldin, Lynn R. ; Stewart, Douglas R.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Human genetics, 2015-07, Vol.134 (7), p.775-787
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ArticlesPeer ReviewedFull Text
Tumors displaying hybrid schwannoma and neurofibroma features in patients with neurofibromatosis type 2
Author / Creator:Montgomery, Blake K. ; Alimchandani, Meghna ; Mehta, Gautam U. ; Dewan, Ramita ; Nesvick, Cody L. ; Miettinen, Markku ; Heiss, John D. ; Asthagiri, Ashok R. ; Quezado, Martha ; Germanwala, Anand V.
Publisher:Germany: Dustri - Verlag Dr. Karl Feistle GmbH & Co. KG
Journal title:Clinical neuropathology, 2016-03, Vol.35 (3), p.78-83
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Amyotrophic lateral sclerosis is over-represented in two Huntington’s disease brain bank cohorts: further evidence to support genetic pleiotropy of pathogenic HTT gene expansion

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Comparative clinical and genomic analysis of neurofibromatosis type 2-associated cranial and spinal meningiomas

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In search of genetic factors predisposing to familial hairy cell leukemia (HCL): exome-sequencing of four multiplex HCL pedigrees

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The Association of CD81 Polymorphisms with Alloimmunization in Sickle Cell Disease

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Age-related accumulation of T cells with markers of relatively stronger autoreactivity leads to functional erosion of T cells

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Plasma microRNA signature as biomarker for disease progression in frontotemporal dementia and amyotrophic lateral sclerosis

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Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation

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Intermediate HTT CAG repeats worsen disease severity in amyotrophic lateral sclerosis

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First insight into the somatic mutation burden of neurofibromatosis type 2-associated grade I and grade II meningiomas: a case report comprehensive genomic study of two cranial meningiomas with vastly...

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Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large family

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Tumors displaying hybrid schwannoma and neurofibroma features in patients with neurofibromatosis type 2

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