Michael C. Kruer

12.8k citations

74 papers · 2.2k indexed · 1 hit paper · h-index 25

Impact in

Neurology top 2%
- Autoimmune Neurological Disorders and Treatments
- Neurological diseases and metabolism
- Peripheral Neuropathies and Disorders
Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders

Papers in

Neurology 26
- Neurological disorders and treatments 12
- Neurological diseases and metabolism 12
- Botulinum Toxin and Related Neurological Disorders 8
Psychiatry and Mental health 23
- Cerebral Palsy and Movement Disorders 16

Co-authors: Josep Dalmau Nathalie Boddaert Allison Gregory Susan J. Hayflick Michael Fahey Luís Bataller Francesc Graus Eugenia Martínez‐Hernández
Journals: Neurology (4 papers)Neurology Genetics (4 papers)Annals of Neurology (4 papers)Human Molecular Genetics (3 papers)PEDIATRICS (3 papers)
Partner nations: United States Australia Canada

In The Last Decade

Michael C. Kruer

68 papers receiving 2.2k citations

Hit Papers

align trajectories log scale

Encephalitis with refractory seizures, status epilepticus, and antibodies to the GABAA receptor: a case series, characterisation of the antigen, and analysis of the effects of antibodies 2014 · 404 citations

Peers

Countries citing papers authored by Michael C. Kruer

Since Specialization

Citations

This map shows the geographic impact of Michael C. Kruer's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Michael C. Kruer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael C. Kruer more than expected).

Fields of papers citing papers by Michael C. Kruer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael C. Kruer. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Michael C. Kruer. The network helps show where Michael C. Kruer may publish in the future.

Co-authors

The 25 scholars most cited alongside Michael C. Kruer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Michael C. Kruer Line = papers co-authored together Michael C. Kruer links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Chronic Striatal Cholinergic Interneuron Excitation Causes Cerebral Palsy‐Related Dystonic Behavior in Mice Annals of Neurology ·Kat Gemperli, Xinguo Lu, Keerthana Chintalapati, Alyssa Rust, Rishabh Bajpai, Nathan Suh, Joanna Blackburn, Rose Gelineau‐Morel, Michael C. Kruer, Dararat Mingbunjerdsuk, Jennifer A. O’Malley, Laura Tochen, Jeff L. Waugh, Steve W. Wu, Timothy Feyma, Joel S. Perlmutter, Steven Mennerick, Jordan G. McCall, Bhooma R. Aravamuthan	2025	0
2	Multicenter Improvement in Screening for Dystonia in Young People With Cerebral Palsy Neurology Clinical Practice ·Bhooma R. Aravamuthan, Emma Lott, Esra Pehlivan, Keerthana Chintalapati, Deborah Grenard, Desiree Roge, Rose Gelineau‐Morel, (unknown), Christie Becu, Michael C. Kruer, Linn Katus, Paul Gross, Amy F. Bailes	2025	0
3	Potential utility of local field potentials to guide DBS programming in pediatric dystonia Brain stimulation ·Michael C. Kruer	2025	0
4	Uncertainties Regarding Cerebral Palsy Diagnosis Neurology Clinical Practice ·Bhooma R. Aravamuthan, Darcy Fehlings, Iona Novak, Paul Gross, Noor Alyasiry, Ann Tilton, Michael Shevell, Michael Fahey, Michael C. Kruer	2024	10
5	Antibodies Against ZSCAN1 in Pediatric and Adult Patients With Non-Paraneoplastic ROHHAD Syndrome Neurology Neuroimmunology & Neuroinflammation ·Ana Beatriz Serafim, Gemma Olivé-Cirera, Ángel Ortega‐González, Michael C. Kruer, Debra E. Weese‐Mayer, Casey M. Rand, Carmen Fons, Joaquín Alejandro Fernández‐Ramos, Maria Grazia Clemente, Mateus Mistieri Simabukuro, Emília Katiane Embiruçu, Salvador Ibáñez‐Micó, Josep Dalmau, Francesc Graus, Thaís Armangué, Lídia Sabater	2024	3
6	Emerging Subspecialties: Pediatric Movement Disorders Neurology Neurology ·S. K. Kahlon, Christopher Barton, Amal Abu Libdeh, Jennifer A. O’Malley, Toni S. Pearson, Jeff L. Waugh, Steve W. Wu, Alonso Zea Vera, Michael C. Kruer	2023	0
7	AGAP1-associated endolysosomal trafficking abnormalities link gene–environment interactions in neurodevelopmental disorders Disease Models & Mechanisms ·Sara A. Lewis, Somayeh Bakhtiari, Jacob Forstrom, Allan Bayat, Frédéric Bilan, Gwenaël Le Guyader, Ebba Alkhunaizi, Hilary J. Vernon, Sergio Padilla‐Lopez, Michael C. Kruer	2023	5
8	A biallelic loss-of-function variant in TMEM147 causes profound intellectual disability and spasticity Neurogenetics ·Tahereh Ghorashi, Hossein Darvish, Somayeh Bakhtiari, Abbas Tafakhori, Michael C. Kruer, Hossein Mozdarani	2023	0
9	GRM7-related disorder: five additional patients from three independent families and review of the literature European Journal of Medical Genetics ·Louis Januel, Nicolas Chatron, Clotilde Rivier-Ringenbach, Sara Cabet, Audrey Labalme, Yavuz Şahin, Hossein Darvish, Michael C. Kruer, Somayeh Bakhtiari, Damien Sanlaville, Jean Madeleine de Sainte Agathe, Gaëtan Lesca	2023	2
10	Top 10 Research Themes for Dystonia in Cerebral Palsy Neurology ·Laura Gilbert, Darcy Fehlings, Paul Gross, Michael C. Kruer, Wendy Kwan, Jonathan W. Mink, Michele Shusterman, Bhooma R. Aravamuthan	2022	13
11	The phenotypic spectrum of PCDH12 associated disorders - Five new cases and review of the literature European Journal of Paediatric Neurology ·Walid Fazeli, Daniel Bamborschke, Abubakar Moawia, Somayeh Bakhtiari, Abbas Tafakhori, Matthias Giersdorf, Andreas Hahn, Anja Weik, Kirsten Kolzter, Sajad Shafiee, Sheng Chih Jin, Friederike Körber, Min Ae Lee‐Kirsch, Hossein Darvish, Sebahattin Çırak, Michael C. Kruer, Anne Koy	2021	5
12	Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities Disease Models & Mechanisms ·Michelle Stewart, Petrina Lau, Gareth Banks, Rasneer Sonia Bains, Enrico Castroflorio, Peter L. Oliver, Christine L. Dixon, Michael C. Kruer, Dimitri M. Kullmann, Abraham Acevedo‐Arozena, Sara Wells, Silvia Corrochano, Patrick M. Nolan	2019	19
13	A Scale to Assess Activities of Daily Living in Pantothenate Kinase‐Associated Neurodegeneration Movement Disorders Clinical Practice ·Randall D. Marshall, Abigail Collins, Maria L. Escolar, Hyder A. Jinnah, Thomas Klopstock, Michael C. Kruer, Aleksandar Videnović, Amy Robichaux‐Viehoever, Laura Swett, Dennis A. Revicki, Randall H. Bender, William R. Lenderking	2018	8
14	Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48) Neurology Genetics ·Jennifer Hirst, Marianna Madeo, Katrien Smets, James R. Edgar, Lüdger Schöls, Jun Li, Anna Yarrow, Tine Deconinck, Jonathan Baets, Elisabeth Van Aken, Jan De Bleecker, Manuel B. Datiles, Ricardo H. Roda, Joachim Liepert, Stephan Züchner, Caterina Mariotti, Peter De Jonghe, Craig Blackstone, Michael C. Kruer	2016	24
15	Further supporting evidence for the SATB2‐associated syndrome found through whole exome sequencing American Journal of Medical Genetics Part A ·Yuri A. Zárate, Hazel Perry, Tawfeg Ben‐Omran, Elizabeth A. Sellars, Quinn Stein, Mariam Al‐Mureikhi, Kirk Simmons, Ophir D. Klein, Jennifer L. Fish, Murray Feingold, Jessica Douglas, Michael C. Kruer, Yue Si, Rong Mao, Dianalee McKnight, Federica Gibellini, Kyle Retterer, Anne Slavotinek	2015	37
16	C19orf12 mutation leads to a pallido-pyramidal syndrome Gene ·Michael C. Kruer, Mustafa A. Salih, Catherine Mooney, Jawahir Al-Zahrani, Salah A. Elmalik, Mohammad M. Kabiraj, Arif O. Khan, Reema Paudel, Henry Houlden, Hamid Azzedine, Fowzan S. Alkuraya	2013	22
17	Novel histopathologic findings in molecularly-confirmed pantothenate kinase-associated neurodegeneration Brain ·Michael C. Kruer, M. Hiken, Allison Gregory, Alessandro Malandrini, David G. Clark, P. Hogarth, Marjorie R. Grafe, Susan J. Hayflick, R. L. Woltjer	2011	99
18	Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA) Annals of Neurology ·Michael C. Kruer, Coro Paisán‐Ruíz, Nathalie Boddaert, Moon Young Yoon, Hiroko Hama, Allison Gregory, Alessandro Malandrini, Randall L. Woltjer, Arnold Münnich, Stéphanie Gobin, Brenda J. Polster, Silvia Palmeri, Simon Edvardson, John Hardy, Henry Houlden, Susan J. Hayflick	2010	163
19	The value of positron emission tomography and proliferation index in predicting progression in low-grade astrocytomas of childhood Journal of Neuro-Oncology ·Michael C. Kruer, Allen M. Kaplan, Michael Etzl, David Carpentieri, Paul S. Dickman, Kewei Chen, Kathleen Mathieson, Alison Irving	2009	24
20	Identification of disease causing loci using an array-based genotyping approach on pooled DNA BMC Genomics ·David W. Craig, Matthew J. Huentelman, Diane Hu‐Lince, Victoria Zismann, Michael C. Kruer, Anne M. Lee, Erik G. Puffenberger, John Pearson, Dietrich Stephan	2005	54

About Michael C. Kruer

Michael C. Kruer is a scholar working on Neurology, Neurology, Psychiatry and Mental health, Genetics and Clinical Biochemistry, having authored 74 papers that have together received 2.2k indexed citations. Recurring topics across this work include Cerebral Palsy and Movement Disorders (16 papers), Neurological disorders and treatments (12 papers), Neurological diseases and metabolism (12 papers), Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (12 papers), Botulinum Toxin and Related Neurological Disorders (8 papers), Porphyrin Metabolism and Disorders (7 papers) and Neonatal and fetal brain pathology (6 papers). The work is most often cited by research in Neurology (501 citations), Neurology (901 citations), Clinical Biochemistry (204 citations), Cellular and Molecular Neuroscience (449 citations) and Psychiatry and Mental health (342 citations). Michael C. Kruer has collaborated with scholars based in United States, Australia and Canada. Frequent co-authors include Josep Dalmau, Nathalie Boddaert, Allison Gregory, Susan J. Hayflick, Michael Fahey, Luís Bataller, Francesc Graus, Eugenia Martínez‐Hernández, Thaís Armangué and Henry Houlden. Their work appears in journals such as Neurology, Neurology Genetics, Annals of Neurology, Human Molecular Genetics and PEDIATRICS.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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