Steven L. Roberds

8.5k citations

49 papers · 3.6k indexed · 1 hit paper · h-index 25

Cellular and Molecular Neuroscience top 2%
- Neuroscience and Neural Engineering 5
Molecular Biology top 2%
- Muscle Physiology and Disorders 18
- Ion channel regulation and function 8
Cardiology and Cardiovascular Medicine top 2%
- Cardiac electrophysiology and arrhythmias 6
- Cardiomyopathy and Myosin Studies 5
Physiology top 2%
- Tuberous Sclerosis Complex Research 7
- Adipose Tissue and Metabolism 6
Cell Biology top 2%
Genetics
- Neurogenetic and Muscular Disorders Research 5

Co-authors: Kevin P. Campbell Michael M. Tamkun Richard H. Scheller Richard D. Anderson John P. Merlie Oxana Ibraghimov‐Beskrovnaya Elizabeth D. Apel Dirk J. Snyders
Cited by: Cellular and Molecular Neuroscience Molecular Biology Cardiology and Cardiovascular Medicine
Journals: Cell (2 papers)Proceedings of the National Academy of Sciences (1 paper)Nucleic Acids Research (1 paper)
Partner nations: United States Sweden France

In The Last Decade

Steven L. Roberds

47 papers receiving 3.5k citations

Hit Papers

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Peers

Countries citing papers authored by Steven L. Roberds

Since Specialization

Citations

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

Fields of papers citing papers by Steven L. Roberds

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Steven L. Roberds. 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 Steven L. Roberds. The network helps show where Steven L. Roberds may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Cutaneous manifestations-associated with tuberous sclerosis complex and the use of topical rapamycin in the United States: a sub-analysis of an international survey of caregivers and patients Orphanet Journal of Rare Diseases ·Sreedevi Boggarapu,Gabrielle V. Rushing,Ashley Pounders,Steven L. Roberds,Eric Beresford	2025	0
2	The role of the TSC Alliance in advancing therapy development: a patient organization perspective PubMed ·Steven L. Roberds,Zoë Fuchs,Elizabeth M. Cassidy,Samantha Metzger,Ayat Abi,Ashley Pounders,Dean J. Aguiar	2024	0
3	Inhibition of MEK-ERK signaling reduces seizures in two mouse models of tuberous sclerosis complex Epilepsy Research ·Lena H. Nguyen,Steven C. Leiser,Dekun Song,Daniela Brunner,Steven L. Roberds,Michael Wong,Angélique Bordey	2022	16
4	Epilepsy Community at an Inflection Point: Translating Research Toward Curing the Epilepsies and Improving Patient Outcomes Epiliepsy currents ·Ilene Miller,JayEtta Hecker,Brandy Fureman,Mary Anne Meskis,Steven L. Roberds,Monika Jones,Heidi L. Grabenstatter,Vanessa Vogel‐Farley,Laura S. Lubbers	2021	2
5	Approach to Preventive Epilepsy Treatment in Tuberous Sclerosis Complex and Current Clinical Practice in 23 Countries Pediatric Neurology ·Monika Słowińska,Katarzyna Kotulska,Sylwia Szymańska,Steven L. Roberds,Carla Fladrowski,Sergiusz Jóźwiak	2020	17
6	Novel brain permeant mTORC1/2 inhibitors are as efficacious as rapamycin or everolimus in mouse models of acquired partial epilepsy and tuberous sclerosis complex Neuropharmacology ·Wiebke Theilmann,Birthe Gericke,Alina Schidlitzki,Syed Muhammad Muneeb Anjum,Saskia Borsdorf,Timon Harries,Steven L. Roberds,Dean J. Aguiar,Daniela Brunner,Steven C. Leiser,Dekun Song,Doriano Fabbro,Petra Hillmann,Matthias P. Wymann,Wolfgang Löscher	2020	23
7	The Impact of Psychiatric Symptoms on Tuberous Sclerosis Complex and Utilization of Mental Health Treatment Pediatric Neurology ·Kate Mowrey,Myla Ashfaq,Deborah A. Pearson,S. Shahrukh Hashmi,Steven L. Roberds,Laura S. Farach,Hope Northrup	2018	6
8	Exploring the foundation of genomics: a Northern blot reference set for the comparative analysis of transcript profiling technologies Comparative and Functional Genomics ·Danielle Kemmer,Margareta Faxén,Emily Hodges,Jonathan Lim,Elena Herzog,Elsebrit Ljungström,Anders Lundmark,Mary K. Olsen,Raf M. Podowski,Erik L. L. Sonnhammer,Peter Nilsson,Mark Reimers,Boris Lenhard,Steven L. Roberds,Claes Wahlestedt,Christer Höög,Pankaj Agarwal,Wyeth W. Wasserman	2004	1
9	A cluster of novel serotonin receptor 3-like genes on human chromosome 3 Gene ·Alla Karnovsky,Lisa F. Gotow,Denise D. McKinley,Julie L. Piechan,Cara Ruble,Cynthia Mills,Kathleen A.B. Schellin,Jerry L. Slightom,Laura R. Fitzgerald,C W Benjamin,Steven L. Roberds	2003	69
10	Characterization and Expression of Nicotinic ACh Receptors in the Mammalian Retina Investigative Ophthalmology & Visual Science ·Linn Dm,L Cortes-Borgos,P McFinton,Lisa Gotow,Martin Aastrup Olsen,Steven L. Roberds,Eh F Wong	2002	3
11	BACE knockout mice are healthy despite lacking the primary beta-secretase activity in brain: implications for Alzheimer's disease therapeuticsbreakdown → Human Molecular Genetics ·Steven L. Roberds	2001	557
12	A 5′ Dystrophin Duplication Mutation Causes Membrane Deficiency of -Dystroglycan in a Family with X-linked Cardiomyopathy Journal of Molecular and Cellular Cardiology ·Roger D. Bies,Masato Maeda,Steven L. Roberds,Emma Holder,Teresa Bohlmeyer,James B. Young,Kevin P. Campbell	1997	46
13	CLINICAL AND MOLECULAR PATHOLOGICAL FEATURES OF SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY IN SAUDI ARABIA Developmental Medicine & Child Neurology ·Mustafa A. Salih,A Maluli,ACAl Rikabi,M. Al‐Bunycin,Steven L. Roberds,Richard D. Anderson,Kevin P. Campbell	1996	11
14	Expression of Deletion-Containing Dystrophins in mdx Muscle: Implications for Gene Therapy and Dystrophin Function Pediatric Research ·Jeffery D. Fritz,István Dankó,Steven L. Roberds,Kevin P. Campbell,Jeffrey S. Latendresse,Jon A. Wolff	1995	12
15	A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy Human Molecular Genetics ·(unknown),Eloísa S. Moreira,Mariz Vainzof,Jeffrey S. Chamberlain,S. K. Marle,Leandro de Mattos Pereira,Jennifer A. Akiyama,Steven L. Roberds,Kevin P. Campbell,Mayana Zatz	1995	57
16	α‐Dystroglycan deficiency correlates with elevated serum creatine kinase and decreased muscle contraction tension in golden retriever muscular dystrophy FEBS Letters ·James M. Ervasti,Steven L. Roberds,Richard D. Anderson,Nicholas Sharp,Joe N. Kornegay,Kevin P. Campbell	1994	12
17	Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin. Journal of Clinical Investigation ·I. Higuchi,Hirotsugu Yamada,Hidetoshi Fukunaga,Hiroyuki Iwaki,R Okubo,M. Nakagawa,Mitsuhiro Osame,Steven L. Roberds,T. Shimizu,Kevin P. Campbell	1994	27
18	Molecular Biology of the Voltage‐Gated Potassium Channels of the Cardiovascular System Journal of Cardiovascular Electrophysiology ·Steven L. Roberds,Karen M. Knoth,Sunny S. Po,Thomas A. Blair,Paul B. Bennett,R P Hartshorne,Dirk J. Snyders,Michael M. Tamkun	1993	56
19	Functional characterization of RK5, a voltage‐gated K⁺ channel cloned from the rat cardiovascular system FEBS Letters ·Thomas A. Blair,Steven L. Roberds,M M Tamkun,R P Hartshorne	1991	54
20	Highly degenerate, inosine-containing primers specifically amplify rare cDNA using the polymerase chain reaction Nucleic Acids Research ·K Knoth,Steven L. Roberds,C Poteet,M M Tamkun	1988	89

About Steven L. Roberds

Steven L. Roberds is a scholar working on Genetics, Biochemistry and Physiology, having authored 49 papers that have together received 3.6k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (18 papers), Ion channel regulation and function (8 papers), Tuberous Sclerosis Complex Research (7 papers), Cardiac electrophysiology and arrhythmias (6 papers), Adipose Tissue and Metabolism (6 papers), Neuroscience and Neural Engineering (5 papers), Cardiomyopathy and Myosin Studies (5 papers) and Neurogenetic and Muscular Disorders Research (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.1k citations), Molecular Biology (2.7k citations) and Cardiology and Cardiovascular Medicine (862 citations). Steven L. Roberds has collaborated with scholars based in United States, Sweden and France. Frequent co-authors include Kevin P. Campbell, Michael M. Tamkun, Richard H. Scheller, Richard D. Anderson, John P. Merlie, Oxana Ibraghimov‐Beskrovnaya, Elizabeth D. Apel, Dirk J. Snyders, Paul B. Bennett and Sunny S. Po. Their work appears in journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

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