ScholarIQanswers from OpenAlex & ORCID
Frederick W. Miller
ResearcherPublications, citations & collaboration network
Frederick W. Miller is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Frederick W. Miller have?
ScholarIQindexed works
Frederick W. Miller has 667 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Frederick W. Miller have?
ScholarIQcitation count
Frederick W. Miller has 34,900 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Frederick W. Miller?
ScholarIQh-index
Frederick W. Miller has an h-index of 97 in OpenAlex.
What is the i10-index of Frederick W. Miller?
ScholarIQi10-index
Frederick W. Miller has an i10-index of 364 in OpenAlex.
What is the ORCID of Frederick W. Miller?
ScholarIQorcid
The ORCID for Frederick W. Miller is on the source record.
What is the OpenAlex record for Frederick W. Miller?
ScholarIQopenalex
The OpenAlex for Frederick W. Miller is on the source record.
What are the most-cited papers on Frederick W. Miller?
ScholarIQmost cited works
2017 European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups
Ingrid E. Lundberg, Anna Tjärnlund, Matteo Bottai, Victoria P. Werth, Clarissa Pilkington, Marianne de Visser, Lars Alfredsson, Anthony A. Amato, Richard J. Barohn, Matthew H. Liang, Jasvinder A. Singh, Rohit Aggarwal, Snjólaug Arnardottir, Hector Chinoy, Robert G. Cooper, Katalin Dankó, Mazen M. Dimachkie, Brian M. Feldman, Ignacio García‐De La Torre, Patrick Gordon, Taichi Hayashi, James D. Katz, Hitoshi Kohsaka, Peter A. Lachenbruch, Bianca Lang, Yuhui Li, Chester V. Oddis, Marzena Olesińska, Ann M. Reed, Lidia Rutkowska‐Sak, Helga Sanner, Albert Selva-O’Callaghan, Yeong‐Wook Song, Jiří Vencovský, Steven R. Ytterberg, Frederick W. Miller, Lisa G. Rider
2017 European League Against Rheumatism/American College of Rheumatology Classification Criteria for Adult and Juvenile Idiopathic Inflammatory Myopathies and Their Major Subgroups
Ingrid E. Lundberg, Anna Tjärnlund, Matteo Bottai, Victoria P. Werth, Clarissa Pilkington, Marianne de Visser, Lars Alfredsson, Anthony A. Amato, Richard J. Barohn, Matthew H. Liang, Jasvinder A. Singh, Rohit Aggarwal, Snjólaug Arnardottir, Hector Chinoy, Robert G. Cooper, Katalin Dankó, Mazen M. Dimachkie, Brian M. Feldman, Ignacio García‐De La Torre, Patrick Gordon, Taichi Hayashi, James D. Katz, Hitoshi Kohsaka, Peter A. Lachenbruch, Bianca Lang, Yuhui Li, Chester V. Oddis, Marzena Olesińska, Ann M. Reed, Lidia Rutkowska‐Sak, Helga Sanner, Albert Selva-O’Callaghan, Yeong‐Wook Song, Jiří Vencovský, Steven R. Ytterberg, Frederick W. Miller, Lisa G. Rider
Aristolochic acid and the etiology of endemic (Balkan) nephropathy
Arthur P. Grollman, Shinya Shibutani, Masaaki Moriya, Frederick W. Miller, Lin Wu, Ute M. Moll, Naomi Suzuki, Andrea Fernandes, Thomas A. Rosenquist, Zvonimir Medverec, Krunoslav Jakovina, Branko Brdar, Neda Slade, Robert J. Turesky, Angela K. Goodenough, Robert Rieger, Mato Vukelić, Bojan Jelaković
Measures of adult and juvenile dermatomyositis, polymyositis, and inclusion body myositis: Physician and Patient/Parent Global Activity, Manual Muscle Testing (MMT), Health Assessment Questionnaire (HAQ)/Childhood Health Assessment Questionnaire (C‐HAQ), Childhood Myositis Assessment Scale (CMAS), Myositis Disease Activity Assessment Tool (MDAAT), Disease Activity Score (DAS), Short Form 36 (SF‐36), Child Health Questionnaire (CHQ), Physician Global Damage, Myositis Damage Index (MDI), Quantitative Muscle Testing (QMT), Myositis Functional Index‐2 (FI‐2), Myositis Activities Profile (MAP), Inclusion Body Myositis Functional Rating Scale (IBMFRS), Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI), Cutaneous Assessment Tool (CAT), Dermatomyositis Skin Severity Index (DSSI), Skindex, and Dermatology Life Quality Index (DLQI)
Lisa G. Rider, Victoria P. Werth, Adam M. Huber, Helene Alexanderson, Anand Rao, Nicolino Ruperto, Laura Herbelin, Richard J. Barohn, David Isenberg, Frederick W. Miller
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups
Simon Rothwell, Robert G. Cooper, Ingrid E. Lundberg, Frederick W. Miller, Peter K. Gregersen, John Bowes, Jiří Vencovský, Katalin Dankó, Vidya Limaye, Albert Selva-O’Callaghan, Michael G. Hanna, Pedro Machado, Lauren M. Pachman, Ann M. Reed, Lisa G. Rider, Joanna Cobb, Hazel Platt, Øyvind Molberg, Olivier Benvéniste, Pernille Mathiesen, Timothy Radstake, Andrea Doria, Jan De Bleecker, Boél De Paepe, Britta Maurer, William Ollier, Leonid Padyukov, Terrance P. OʼHanlon, Annette Lee, Christopher I. Amos, Christian Gieger, Thomas Meitinger, Juliane Winkelmann, Lucy R. Wedderburn, Hector Chinoy, Janine A. Lamb