Stephen R. Dlouhy

2.7k citations

59 papers · 1.9k indexed · h-index 25

Neurology top 1%
- Neurological diseases and metabolism 11
Nutrition and Dietetics top 2%
- Trace Elements in Health 8
Developmental Neuroscience top 5%
Molecular Biology top 5%
- Prion Diseases and Protein Misfolding 14
- Mitochondrial Function and Pathology 4
Cellular and Molecular Neuroscience top 5%
- Hereditary Neurological Disorders 6
Genetics
- Connective tissue disorders research 6
Physiology
- Salivary Gland Disorders and Functions 4
- Alzheimer's disease research and treatments 4

Co-authors: Bernardino Ghetti M. E. Hodes Martin R. Farlow Robert C. Karn Fabrizio Tagliavini Orso Bugiani Giorgio Giaccone Karen Hsiao
Cited by: Neurology Nutrition and Dietetics Developmental Neuroscience
Journals: Cell (1 paper)Neuron (1 paper)Nature Genetics (2 papers)
Partner nations: United States Italy United Kingdom

In The Last Decade

Stephen R. Dlouhy

59 papers receiving 1.8k citations

Peers

Countries citing papers authored by Stephen R. Dlouhy

Since Specialization

Citations

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

Fields of papers citing papers by Stephen R. Dlouhy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephen R. Dlouhy. 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 Stephen R. Dlouhy. The network helps show where Stephen R. Dlouhy may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	The progression of Wiedemann–Steiner syndrome in adulthood and two novel variants in the KMT2A gene American Journal of Medical Genetics Part A ·Hailey R. Feldman,Stephen R. Dlouhy,Melissa Lah,Katelyn Payne,David D. Weaver	2018	10
2	The novel Tau mutation G335S: clinical, neuropathological and molecular characterization Acta Neuropathologica ·Salvatore Spina,Jill R. Murrell,Hirotaka Yoshida,Bernardino Ghetti,Niamh Bermingham,Brian Sweeney,Stephen R. Dlouhy,R. Anthony Crowther,Michel Goedert,Catherine Keohane	2006	25
3	Prion Proteins with Different Conformations Accumulate in Gerstmann-Sträussler-Scheinker Disease Caused by A117V and F198S Mutations American Journal Of Pathology ·Pedro Piccardo,Juris J. Liepnieks,Albert William,Stephen R. Dlouhy,Martin R. Farlow,Katherine Young,David Nochlin,Thomas D. Bird,Randal R. Nixon,Melvyn J. Ball,Charles DeCarli,Orso Bugiani,Fabrizio Tagliavini,Merrill D. Benson,Bernardino Ghetti	2001	68
4	Additional Copies of the Proteolipid Protein Gene Causing Pelizaeus-Merzbacher Disease Arise by Separate Integration into the X Chromosome The American Journal of Human Genetics ·M. E. Hodes,Karen Woodward,Nancy B. Spinner,Beverly S. Emanuel,Agnes Enrico-Simon,John Kamholz,Dwight Stambolian,Elaine H. Zackai,Victoria M. Pratt,I. T. Thomas,Keith A. Crandall,Stephen R. Dlouhy,Sue Malcolm	2000	37
5	X-linked spastic paraplegia due to a mutation (C506T; Ser169Phe) in exon 4 of the proteolipid protein gene (PLP) American Journal of Medical Genetics ·M. E. Hodes,Andreas Hadjisavvas,Ian J. Butler,Antonina Aydanian,Stephen R. Dlouhy	1998	9
6	Characterization of MurineGirk2Transcript Isoforms: Structure and Differential Expression Genomics ·Jian‐Jun Wei,M. E. Hodes,Roberto Piva,Yue Feng,Yi Wang,Bernardino Ghetti,Stephen R. Dlouhy	1998	45
7	Hypothalamic-Pituitary-Gonadal Axis in the Mutant Weaver Mouse Neuroendocrinology ·Neena B. Schwartz,Márta Szabó,Tatyana Verina,Jian‐Jun Wei,Stephen R. Dlouhy,Lisa Won,Alfred Heller,M. E. Hodes,Bernardino Ghetti	1998	12
8	In Situ Hybridization Analysis of Girk2 Expression in the Developing Central Nervous System in Normal and Weaver Mice Journal of Neuropathology & Experimental Neurology ·Jianjun Wei,Stephen R. Dlouhy,Shirley A. Bayer,Roberto Piva,Tatyana Verina,Yi Wang,Yue Feng,Brenda Dupree,M. E. Hodes,Bernardino Ghetti	1997	2
9	Proteolipid Protein Is Necessary in Peripheral as Well as Central Myelin Neuron ·James Garbern,Franca Cambi,Xue-Ming Tang,Anders A. F. Sima,J.M. Vallat,E. Peter Bosch,Richard A. Lewis,Michael E. Shy,Jasloveleen Sohi,George H. Kraft,Ke Lian Chen,Indira Joshi,Debra G. B. Leonard,William G. Johnson,Wendy H. Raskind,Stephen R. Dlouhy,Victoria M. Pratt,M. E. Hodes,Thomas D. Bird,John Kamholz	1997	111
10	A Reintroduction to Mendelian Genetics Cancer Investigation ·M. E. Hodes,Stephen R. Dlouhy	1997	1
11	Prion Protein Amyloidosis Brain Pathology ·Bernardino Ghetti,Pedro Piccardo,B Frangione,Orso Bugiani,Giorgio Giaccone,Katherine Young,Frances Prelli,Martin R. Farlow,Stephen R. Dlouhy,Fabrizio Tagliavini	1996	148
12	Phenotypic effects of the weaver gene are evident in the embryonic cerebellum but not in the ventral midbrain Developmental Brain Research ·Shirley A. Bayer,Katherine V. Wills,Jian‐Jun Wei,Yue Feng,Stephen R. Dlouhy,M. E. Hodes,Tatyana Verina,Bernardino Ghetti	1996	19
13	Girl with signs of Pelizaeus‐Merzbacher disease heterozygous for a mutation in exon 2 of the proteolipid protein gene American Journal of Medical Genetics ·M. E. Hodes,William DeMyer,Victoria M. Pratt,Mary K. Edwards,Stephen R. Dlouhy	1995	29
14	Gerstmann‐Sträussler‐Scheinker Disease and the Indiana Kindred Brain Pathology ·Bernardino Ghetti,Stephen R. Dlouhy,Giorgio Giaccone,Orso Bugiani,Blas Frangione,Martin R. Farlow,Fabrizio Tagliavini	1995	103
15	Gerstmann-Sträussler-Scheinker Disease (PRNP P102L): Amyloid Deposits Are Best Recognized by Antibodies Directed to Epitopes in PrP Region 90-165 Journal of Neuropathology & Experimental Neurology ·Pedro Piccardo,Bernardino Ghetti,Dennis W. Dickson,Harry V. Vinters,Orso Bugiani,Fabrizio Tagliavini,D katherine Young,Stephen R. Dlouhy,Charles E. Seiler,Carrie K. Jones,Alice Lazzarini,Lawrence I. Golbe,Thomas Zimmerman,Susan Perlman,D. C. McLachlan,Peter St George‐Hyslop,Anne Lennox,Giorgio Giaccone	1995	25
16	Pelizaeus‐Merzbacher disease in a family of Portuguese origin caused by a point mutation in exon 5 of the proteolipid protein gene American Journal of Medical Genetics ·Victoria M. Pratt,Simon Boyadjiev,Stephen R. Dlouhy,Kenneth Silver,Vazken M. Der Kaloustian,M. E. Hodes	1995	9
17	Analysis of region-specific library constructed by sequence-independent amplification of microdissected fragments surrounding weaver (wv) gene on mouse chromosome 16 Somatic Cell and Molecular Genetics ·Jian‐Jun Wei,Stephen R. Dlouhy,Jianguo Zhu,Bernardino Ghetti,M. E. Hodes	1994	5
18	Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles Nature Genetics ·Karen Hsiao,Stephen R. Dlouhy,Martin R. Farlow,Carin Cass,Maria Da Costa,P. Michael Conneally,M. E. Hodes,Bernardino Ghetti,Stanley B. Prusiner	1992	174
19	Localization of the gene for X‐linked nephrogenic diabetes insipidus to Xq28 American Journal of Medical Genetics ·Marios Kambouris,Stephen R. Dlouhy,James A. Trofatter,P. Michael Conneally,M. E. Hodes,John M. Optiz,James F. Reynolds	1988	35
20	The Genes for Mouse Salivary Androgen-Binding Protein (ABP) Subunits Alpha and Gamma Are Located on Chromosome 7 Genetics ·Stephen R. Dlouhy,Benjamin A. Taylor,Robert C. Karn	1987	45

About Stephen R. Dlouhy

Stephen R. Dlouhy is a scholar working on Neurology, Developmental Neuroscience and Cellular and Molecular Neuroscience, having authored 59 papers that have together received 1.9k indexed citations. Recurring topics across this work include Prion Diseases and Protein Misfolding (14 papers), Neurological diseases and metabolism (11 papers), Trace Elements in Health (8 papers), Hereditary Neurological Disorders (6 papers), Connective tissue disorders research (6 papers), Mitochondrial Function and Pathology (4 papers), Salivary Gland Disorders and Functions (4 papers) and Alzheimer's disease research and treatments (4 papers). The work is most often cited by research in Neurology (698 citations), Nutrition and Dietetics (446 citations) and Developmental Neuroscience (110 citations). Stephen R. Dlouhy has collaborated with scholars based in United States, Italy and United Kingdom. Frequent co-authors include Bernardino Ghetti, M. E. Hodes, Martin R. Farlow, Robert C. Karn, Fabrizio Tagliavini, Orso Bugiani, Giorgio Giaccone, Karen Hsiao, Stanley B. Prusiner and Pedro Piccardo. Their work appears in journals such as Cell, Neuron and Nature Genetics.

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