Suzanne D. DeBrosse

1.0k citations

17 papers · 422 indexed · h-index 12

Co-authors: Douglas S. Kerr Shulin Zhang Kazuki Okajima Christine Schmotzer Ghunwa Nakouzi Gyula Acsádi Kathryn J. Swoboda Kenneth Silver
Topics: Metabolism and Genetic Disorders (9 papers)Mitochondrial Function and Pathology (5 papers)Epilepsy research and treatment (3 papers)
Cited by: Clinical Biochemistry Biochemistry Genetics
Journals: Annals of Neurology Eye Molecular Genetics and Metabolism
Partner nations: United States Canada Netherlands

In The Last Decade

Suzanne D. DeBrosse

15 papers receiving 418 citations

Peers

Countries citing papers authored by Suzanne D. DeBrosse

Since Specialization

Citations

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

Fields of papers citing papers by Suzanne D. DeBrosse

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Suzanne D. DeBrosse. 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 Suzanne D. DeBrosse. The network helps show where Suzanne D. DeBrosse may publish in the future.

Co-authorship network of co-authors of Suzanne D. DeBrosse

This figure shows the co-authorship network connecting the top 25 collaborators of Suzanne D. DeBrosse. A scholar is included among the top collaborators of Suzanne D. DeBrosse based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Suzanne D. DeBrosse. Suzanne D. DeBrosse is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Case Report: 2-Year-old With Wilms Tumors, Familial Heterozygous DIS3L2 Mutation, and Cutis Marmorata Telangiectatica Congenita 2022 ·Journal of Pediatric Hematology/Oncology ·(unknown),Suzanne D. DeBrosse,Anna L. Mitchell,(unknown),Michelle Merrill	0
2	Kleefstra syndrome: Impact on parents 2020 ·Disability and health journal ·(unknown),(unknown),Suzanne D. DeBrosse	5
3	Utility of specific amino acid ratios in screening for pyruvate dehydrogenase complex deficiencies and other mitochondrial disorders associated with congenital lactic acidosis and newborn screening prospects 2020 ·JIMD Reports ·Jirair K. Bedoyan,(unknown),(unknown),Sharon Linard,(unknown),(unknown),(unknown),(unknown),(unknown),Kandamurugu Manickam,Mari Mori,Dennis Bartholomew,Suzanne D. DeBrosse,Bruce H. Cohen,Sumit Parikh,Douglas S. Kerr	11
4	The expanding phenotype of OFD1‐related disorders: Hemizygous loss‐of‐function variants in three patients with primary ciliary dyskinesia 2019 ·Molecular Genetics & Genomic Medicine ·(unknown),Suzanne D. DeBrosse,(unknown),Steven Strausbaugh,Moira L. Aitken,Margaret Rosenfeld,Whitney Wolf,Michael R. Knowles,Maimoona A. Zariwala	39
5	Electroencephalography and Epilepsy Course at UH Cleveland Medical Center, Cleveland, Ohio, United States 2019 ·Jun Park,Michael W. Devereaux,Hesham Abboud,(unknown),Mark L. Cohen,Marta Couce,Suzanne D. DeBrosse,Philip S. Fastenau,Guadalupe Fernández‐Baca Vaca,Naiara García Losarcos,(unknown),Nuria Lacuey,(unknown),Jonathan Miller,Carol L. Rosen,Asim Shahid,(unknown),(unknown),Hans O. Lüders	0
6	A novel null mutation in the pyruvate dehydrogenase phosphatase catalytic subunit gene (PDP1) causing pyruvate dehydrogenase complex deficiency 2019 ·JIMD Reports ·Jirair K. Bedoyan,Leah Hecht,Shulin Zhang,Stacey Tarrant,Ann M. Bergin,Didem Demirbas,Edward Yang,(unknown),(unknown),Suzanne D. DeBrosse,Charles L. Hoppel,Douglas S. Kerr,Gerard T. Berry	11
7	Mutations inSCN3Acause early infantile epileptic encephalopathy 2018 ·Annals of Neurology ·Tariq Zaman,Ingo Helbig,Ivana Babič Božović,Suzanne D. DeBrosse,(unknown),(unknown),Līvija Medne,Aleš Maver,Borut Peterlin,Katherine L. Helbig,Xiaohong Zhang,Ethan M. Goldberg	68
8	Inborn Errors of Metabolism with Acidosis 2017 ·Pediatric Clinics of North America ·(unknown),Suzanne D. DeBrosse,Shawn E. McCandless	14
9	Fever-Induced Paroxysmal Weakness and Encephalopathy, a New Phenotype of ATP1A3 Mutation 2017 ·Pediatric Neurology ·(unknown),Kenneth Silver,(unknown),Suzanne D. DeBrosse,(unknown),Kathryn J. Swoboda,Gyula Acsádi	47
10	Lethal neonatal case and review of primary short-chain enoyl-CoA hydratase (SCEH) deficiency associated with secondary lymphocyte pyruvate dehydrogenase complex (PDC) deficiency 2017 ·Molecular Genetics and Metabolism ·Jirair K. Bedoyan,Samuel Yang,Sacha Ferdinandusse,Rhona M. Jack,Alexander Miron,(unknown),Suzanne D. DeBrosse,Charles L. Hoppel,Douglas S. Kerr,Ronald J. A. Wanders	33
11	Succinyl-CoA synthetase ( SUCLA2 ) deficiency in two siblings with impaired activity of other mitochondrial oxidative enzymes in skeletal muscle without mitochondrial DNA depletion 2016 ·Molecular Genetics and Metabolism ·Xiaoping Huang,Jirair K. Bedoyan,Didem Demirbas,David J. Harris,Alexander Miron,(unknown),(unknown),Suzanne D. DeBrosse,Lee-Jun Wong,Charles L. Hoppel,Douglas S. Kerr,Irina Anselm,Gerard T. Berry	21
12	Clinical and imaging characteristics of late onset mitochondrial membrane protein-associated neurodegeneration (MPAN) 2016 ·Neurocase ·(unknown),Brian S. Appleby,Mark L. Cohen,Suzanne D. DeBrosse,James B. Leverenz,Bruce L. Miller,Sandra L. Siedlak,Xiongwei Zhu,Alan J. Lerner	13
13	FHF1 (FGF12) epileptic encephalopathy 2016 ·Neurology Genetics ·(unknown),Miranda Splitt,(unknown),Venkateswaran Ramesh,Suzanne D. DeBrosse,(unknown),(unknown),Yaping Yang,Jill A. Rosenfeld,Patrick Cossette,Jacques L. Michaud,Fadi F. Hamdan,Philippe M. Campeau,Berge A. Minassian,(unknown),(unknown),Jeffrey C. Barrett,Matthew E. Hurles	29
14	Arginine:glycine amidinotransferase (AGAT) deficiency: Clinical features and long term outcomes in 16 patients diagnosed worldwide 2015 ·Molecular Genetics and Metabolism ·Sylvia Stöckler‐Ipsiroglu,(unknown),Roberta Battini,Suzanne D. DeBrosse,(unknown),Simon Edvardson,Florian Eichler,(unknown),David M. Koeller,Sonia Nouioua,Mériem Tazir,Ashok Verma,(unknown),Klaas J. Wierenga,(unknown),Victor Wei Zhang,Lee-Jun Wong	45
15	Neurologic Disorders Due to Mitochondrial DNA Mutations 2012 ·Seminars in Pediatric Neurology ·Suzanne D. DeBrosse,Sumit Parikh	10
16	Spectrum of neurological and survival outcomes in pyruvate dehydrogenase complex (PDC) deficiency: Lack of correlation with genotype 2012 ·Molecular Genetics and Metabolism ·Suzanne D. DeBrosse,Kazuki Okajima,Shulin Zhang,Ghunwa Nakouzi,Christine Schmotzer,(unknown),(unknown),(unknown),Douglas S. Kerr	73
17	Dynamic properties of eye movements in mitochondrial chronic progressive external ophthalmoplegia 2007 ·Eye ·Suzanne D. DeBrosse,Eroboghene E. Ubogu,(unknown),Medhat O. Hassan,Richard Leigh	3

About Suzanne D. DeBrosse

Suzanne D. DeBrosse is a scholar working on Clinical Biochemistry, Genetics and Pharmacy, having authored 17 papers that have together received 422 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (5 papers) and Epilepsy research and treatment (3 papers). The work is most often cited by research in Clinical Biochemistry (182 citations), Biochemistry (46 citations) and Genetics (115 citations). Suzanne D. DeBrosse has collaborated with scholars based in United States, Canada and Netherlands. Frequent co-authors include Douglas S. Kerr, Shulin Zhang, Kazuki Okajima, Christine Schmotzer, Ghunwa Nakouzi, Gyula Acsádi, Kathryn J. Swoboda, Kenneth Silver, Jirair K. Bedoyan and Xiaohong Zhang. Their work appears in journals such as Annals of Neurology, Eye 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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