Harold G. Marks

2.8k citations

48 papers · 1.6k indexed · h-index 24

Impact in

Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Neurology top 5%
- Neurological diseases and metabolism
- Botulinum Toxin and Related Neurological Disorders

Papers in

Cellular and Molecular Neuroscience 17
- Genetic Neurodegenerative Diseases 9
- Hereditary Neurological Disorders 8
Psychiatry and Mental health 8

Co-authors: Vicky L. Funanage Benjamin B. Roa P. James B. Dyck Phillip F. Chance James R. Lupski Paul Carango Elena Pegoraro Agustín Legido
Journals: Neurology (7 papers)Pediatric Neurology (5 papers)Journal of Pediatric Orthopaedics (4 papers)Annals of Neurology (4 papers)Molecular Genetics and Metabolism (2 papers)
Partner nations: United States Italy Netherlands

In The Last Decade

Harold G. Marks

48 papers receiving 1.5k citations

Peers

Countries citing papers authored by Harold G. Marks

Since Specialization

Citations

This map shows the geographic impact of Harold G. Marks'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 Harold G. Marks with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Harold G. Marks more than expected).

Fields of papers citing papers by Harold G. Marks

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Harold G. Marks. 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 Harold G. Marks. The network helps show where Harold G. Marks may publish in the future.

Co-authors

The 25 scholars most cited alongside Harold G. Marks, 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 Harold G. Marks Line = papers co-authored together Harold G. Marks links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Dynamics of gene silencing during X inactivation using allele-specific RNA-seq (vol 16, 149, 2015) Genome biology ·Harold G. Marks, Hindrik H. D. Kerstens, Cland Makasson Raphael, Erik Splinter, Rob Dirks, Guido van Mierlo, Onkar Joshi, V.Poornima, Tomas Babak, Cornelis A. Albers, Tüzer Kalkan, Alan Smith, Alice Jouneau, Wouter de Laat, Joost Gribnau, H.G. Stunnenberg	2016	11
2	Early-progressive dilated cardiomyopathy in a family with Becker muscular dystrophy related to a novel frameshift mutation in the dystrophin gene exon 27 Journal of Human Genetics ·Takeshi Tsuda, David Atallah, Yuhong Zhao, Samuel S. Gidding, 弘美姜, Harold G. Marks, Kevin M. Flanigan, Steven A. Moore	2014	15
3	Non-invasive evaluation of buccal respiratory chain enzyme dysfunction in mitochondrial disease: Comparison with studies in muscle biopsy Molecular Genetics and Metabolism ·Michael J. Goldenthal, Teddy Kuruvilla, Shirish Damle, Leon Salganicoff, Franci Sassin, Nidhi Shah, Harold G. Marks, Divya S. Khurana, Ignacio Valencia, Agustín Legido	2011	27
4	Efficacy and Tolerability of Topiramate in Pediatric Migraine Pediatric Neurology ·J. H. Park, Ignacio Valencia, Agustín Legido, Sanjeev V. Kothare, Divya S. Khurana, Sabrina W. Yum, H. Huntley Hardison, Joseph J. Melvin, Harold G. Marks	2009	18
5	Epilepsy and Respiratory Chain Defects in Children with Mitochondrial Encephalopathies Neuropediatrics ·Divya S. Khurana, Leon Salganicoff, M.C. Audy, Elizabeth F. Hobdell, Ignacio Leyva-Valencia, H. Huntley Hardison, Harold G. Marks, Warren D. Grover, Agustín Legido	2008	51
6	Sleep Study Abnormalities in Children With Attention Deficit Hyperactivity Disorder Pediatric Neurology ·Jatinder S. Goraya, J. H. Park, Ignacio Valencia, Joseph Kaleyias, Divya S. Khurana, H. Huntley Hardison, Harold G. Marks, Agustín Legido, Sanjeev V. Kothare	2008	28
7	Spinocerebellar ataxia type 7 mimicking Kearns–Sayre syndrome: A clinical diagnosis is desirable Journal of the Neurological Sciences ·Surya Gupta, Harold G. Marks	2007	6
8	Treatment of Drop Attacks in Coffin-Lowry Syndrome With the Use of Sodium Oxybate Pediatric Neurology ·Sun Jeoung Lee, Yustinus Joko Wahyu Yuniarto, Divya S. Khurana, Harold G. Marks, Sanjeev V. Kothare	2007	10
9	A PLP splicing abnormality is associated with an unusual presentation of PMD Annals of Neurology ·Grace M. Hobson, Zhong Huang, Karen Sperle, Deborah L. Stabley, Harold G. Marks, Franca Cambi	2002	44
10	A new polymorphism in the proteolipid protein (PLP1) gene and its use for carrier detection ofPLP1 gene duplication in Pelizaeus-Merzbacher disease Human Mutation ·Grace M. Hobson, Deborah L. Stabley, Vicky L. Funanage, Harold G. Marks	2001	3
11	Effect of Triplet Repeat Expansion on Chromatin Structure and Expression of DMPK and Neighboring Genes, SIX5 and DMWD, in Myotonic Dystrophy Molecular Genetics and Metabolism ·Såadhanåa Kaòmsala, Roger van Cauwenberghe, Tobias Græsdal, Iris L. Gonzalez, Paul Carango, Harold G. Marks, Vicky L. Funanage	2001	31
12	Molecular genetics of familial spastic paraplegia: a multitude of responsible genes Journal of the Neurological Sciences ·Hisashi Kobayashi, Carlos García, Helen Doran, Harold G. Marks, Eric P. Hoffman	1996	40
13	Congenital muscular dystrophy with primary laminin α2 (merosin) deficiency presenting as inflammatory myopathy Annals of Neurology ·Elena Pegoraro, Jukka Kivelä, Eric P. Hoffman, Pedro Mancías, Steven H. Swerdlow, Radmila B. Raikow, Carlos García, Harold G. Marks, Thomas O. Crawford, Virginia Carver	1996	82
14	Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy Neurology ·Elena Pegoraro, R. Neil Schimke, (unknown), H. Stern, Morena Cadaldini, C. Angelini, Gabriel T. Fantinatti, Judith Carroll, Warren A. Marks, Hans E. Neville, Harold G. Marks, Scott Appleton, Helga V. Toriello, Henry B. Wessel, Juliana Ospina Castro, Saunder Bernes, Steen Christensen, Lee E. Weiss, Eric P. Hoffman	1995	66
15	Dejerine–Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene Nature Genetics ·Benjamin B. Roa, P. James B. Dyck, Harold G. Marks, Phillip F. Chance, James R. Lupski	1993	210
16	Absence of Myotonic Dystrophy Protein Kinase (DMPK) mRNA as a Result of a Triplet Repeat Expansion in Myotonic Dystrophy Genomics ·Paul Carango, Linus Stenborg, Harold G. Marks, Vicky L. Funanage	1993	107
17	Use of computed tomography, magnetic resonance imaging, and localized 1H magnetic resonance spectroscopy in canavan's disease: A case Report Annals of Neurology ·Harold G. Marks, Anoop Pilar, Zhiyue Wang, John A. Detre, Andrew R. Bogdan, Debra A. Gusnard, Robert A. Zimmerman	1991	44
18	Delayed cervical central cord syndrome after trivial trauma Pediatric Emergency Care ·木原智史, Harold G. Marks, Eric N. Faerber, Cassie Tongue	1990	23
19	Magnetic resonance imaging and computed tomography in Pelizaeus-Merzbacher disease Magnetic Resonance Imaging ·Samuel T. Spencer, Harold G. Marks	1990	24
20	Neonatal rhabdomyolysis as a presentation of muscular dystrophy Neurology ·Galen N. Breningstall, Warren D. Grover, Hanne Mari Kristiansen, Harold G. Marks	1988	4

About Harold G. Marks

Harold G. Marks is a scholar working on Cellular and Molecular Neuroscience, Psychiatry and Mental health, Developmental Biology, Clinical Biochemistry and Molecular Biology, having authored 48 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (9 papers), Muscle Physiology and Disorders (8 papers), Hereditary Neurological Disorders (8 papers), Mitochondrial Function and Pathology (6 papers), Cardiomyopathy and Myosin Studies (4 papers), Adipose Tissue and Metabolism (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Peripheral Neuropathies and Disorders (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (685 citations), Neurology (174 citations), Neurology (239 citations), Clinical Biochemistry (86 citations) and Molecular Biology (840 citations). Harold G. Marks has collaborated with scholars based in United States, Italy and Netherlands. Frequent co-authors include Vicky L. Funanage, Benjamin B. Roa, P. James B. Dyck, Phillip F. Chance, James R. Lupski, Paul Carango, Elena Pegoraro, Agustín Legido, Eric P. Hoffman and Robert A. Taylor. Their work appears in journals such as Neurology, Pediatric Neurology, Journal of Pediatric Orthopaedics, Annals of Neurology and Molecular Genetics and Metabolism.

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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