Peter J. Detloff

3.2k citations

41 papers · 2.5k indexed · h-index 22

Impact in

Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases
Neurology top 2%
- Neurological disorders and treatments

Papers in

Cellular and Molecular Neuroscience 27
- Genetic Neurodegenerative Diseases 27
- Neuroscience and Neuropharmacology Research 4
Neurology 10
- Neurological disorders and treatments 8

Co-authors: Roger L. Albin Mary Y. Heng Thomas D. Petes Sara J. Tallaksen‐Greene Michael A. White Kirupa Sathasivam Gillian P. Bates Richard L. M. Faull
Journals: Molecular and Cellular Biology (5 papers)Human Molecular Genetics (4 papers)Journal of Neuroscience (3 papers)Proceedings of the National Academy of Sciences (3 papers)Neurobiology of Disease (3 papers)
Partner nations: United States United Kingdom New Zealand

In The Last Decade

Peter J. Detloff

40 papers receiving 2.5k citations

Peers

Countries citing papers authored by Peter J. Detloff

Since Specialization

Citations

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

Fields of papers citing papers by Peter J. Detloff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter J. Detloff. 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 Peter J. Detloff. The network helps show where Peter J. Detloff may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Estrogen-related receptor gamma is a regulator of mitochondrial, autophagy, and immediate-early gene programs in spiny projection neurons: Relevance for transcriptional changes in Huntington disease Neurobiology of Disease ·Stephanie N. Fox, Cody Savage, Narcy R Amireddy, Laura J. McMeekin, David K. Crossman, Peter J. Detloff, Michelle Gray, Rita M. Cowell	2025	0
2	A Role for PGC-1α in Transcription and Excitability of Neocortical and Hippocampal Excitatory Neurons Neuroscience ·Laura J. McMeekin, Aundrea F. Bartley, A.S. Bohannon, Elena W Adlaf, Thomas van Groen, Stephanie M. Boas, Stephanie N. Fox, Peter J. Detloff, David K. Crossman, Linda Overstreet‐Wadiche, John J. Hablitz, Lynn E. Dobrunz, Rita M. Cowell	2020	19
3	Cell-Specific Deletion of PGC-1α from Medium Spiny Neurons Causes Transcriptional Alterations and Age-Related Motor Impairment Journal of Neuroscience ·Laura J. McMeekin, Ye Li, Stephanie N. Fox, Glenn C. Rowe, David K. Crossman, Jeremy J. Day, Yuqing Li, Peter J. Detloff, Rita M. Cowell	2018	15
4	Sex-dependent behavioral impairments in the HdhQ350/+ mouse line Behavioural Brain Research ·Jessica K. Cao, Peter J. Detloff, Richard G. Gardner, Nephi Stella	2017	7
5	Characterisation of progressive motor deficits in whisker movements in R6/2, Q175 and Hdh knock-in mouse models of Huntington’s disease Journal of Neuroscience Methods ·Huw Garland, Nigel I. Wood, Elizabeth A. Skillings, Peter J. Detloff, A. Jennifer Morton, Robyn A. Grant	2017	8
6	Allelic series of Huntington's disease knock-in mice reveals expression discorrelates Human Molecular Genetics ·Ashish Kumar, Jennifer Zhang, Sara J. Tallaksen‐Greene, Michael R. Crowley, David K. Crossman, A. Jennifer Morton, Thomas van Groen, Inga Kadish, Roger L. Albin, Mathieu Lesort, Peter J. Detloff	2016	13
7	Purkinje cell dysfunction and loss in a knock-in mouse model of Huntington Disease Experimental Neurology ·Sarah Dougherty, John L. Reeves, Mathieu Lesort, Peter J. Detloff, Rita M. Cowell	2012	30
8	Mitochondrial calcium uptake capacity as a therapeutic target in the R6/2 mouse model of Huntington's disease Human Molecular Genetics ·Giselle Perry, Sara J. Tallaksen‐Greene, Ashish Kumar, Mary Y. Heng, Andrew Kneynsberg, Thomas van Groen, Peter J. Detloff, Roger L. Albin, Mathieu Lesort	2010	29
9	In VivoEvidence for NMDA Receptor-Mediated Excitotoxicity in a Murine Genetic Model of Huntington Disease Journal of Neuroscience ·Mary Y. Heng, Peter J. Detloff, Phillip L. Wang, Joe Z. Tsien, Roger L. Albin	2009	89
10	Rodent genetic models of Huntington disease Neurobiology of Disease ·Mary Y. Heng, Peter J. Detloff, Roger L. Albin	2008	116
11	Intraflagellar transport is essential for endochondral bone formation Development ·Courtney J. Haycraft, Qihong Zhang, Buer Song, Walker S. Jackson, Peter J. Detloff, Rosa Serra, Bradley K. Yoder	2006	318
12	Allele-Specific Conditional Destabilization of Glutamine Repeat mRNAs Gene Expression ·Andrew B. Crouse, Peter J. Detloff	2005	1
13	Embryonic stem cells expressing expanded CAG repeats undergo aberrant neuronal differentiation and have persistent Oct-4 and REST/NRSF expression Molecular and Cellular Neuroscience ·Matthew T. Lorincz, Peter J. Detloff, Roger L. Albin, K. Sue O’Shea	2004	11
14	Hprt^(CAG)146 mice: Age of onset of behavioral abnormalities, time course of neuronal intranuclear inclusion accumulation, neurotransmitter marker alterations, mitochondrial function markers, and susceptibility to 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine The Journal of Comparative Neurology ·Sara J. Tallaksen‐Greene, Jared M. Ordway, Andrew B. Crouse, Walker S. Jackson, Peter J. Detloff, Roger L. Albin	2003	8
15	Analysis of the 5′ end of the mouse Elavl1 (mHuA) gene reveals a transcriptional regulatory element and evidence for conserved genomic organization Gene ·Peter H. King, Jonathan Fuller, Burt Nabors, Peter J. Detloff	2000	18
16	Deletion and Replacement of the Mouse Adult β-Globin Genes by a “Plug and Socket” Repeated Targeting Strategy Molecular and Cellular Biology ·Peter J. Detloff, Jada Lewis, Simon W. M. John, W. Ronald Shehee, Robert Langenbach, Nobuyo Maeda, Oliver Smithies	1994	50
17	Measurements of Excision Repair Tracts Formed during Meiotic Recombination in Saccharomyces cerevisiae Molecular and Cellular Biology ·Peter J. Detloff, Thomas D. Petes	1992	11
18	A promoter deletion reduces the rate of mitotic, but not meiotic, recombination at the HIS4 locus in yeast Current Genetics ·Michael A. White, Peter J. Detloff, Micheline K. Strand, Thomas D. Petes	1992	69
19	Repair of Specific Base Pair Mismatches Formed during Meiotic Recombination in the Yeast Saccharomyces cerevisiae Molecular and Cellular Biology ·Peter J. Detloff, Jennifer Sieber, Thomas D. Petes	1991	25
20	Recombination in yeast and the recombinant DNA technology Genome ·Thomas D. Petes, Peter J. Detloff, Sue Jinks-Robertson, S R Judd, Martin Kupiec, Dilip K Nag, Ann E. Stapleton, Lorraine S. Symington, Annette Vincent, Michael A. White	1989	4

About Peter J. Detloff

Peter J. Detloff is a scholar working on Cellular and Molecular Neuroscience, Neurology, Molecular Biology, Clinical Biochemistry and Genetics, having authored 41 papers that have together received 2.5k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (27 papers), Mitochondrial Function and Pathology (18 papers), Fungal and yeast genetics research (9 papers), Neurological disorders and treatments (8 papers), DNA Repair Mechanisms (8 papers), Muscle Physiology and Disorders (6 papers), Neuroscience and Neuropharmacology Research (4 papers) and Metabolism and Genetic Disorders (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.5k citations), Neurology (520 citations), Molecular Biology (2.1k citations), Genetics (419 citations) and Aging (21 citations). Peter J. Detloff has collaborated with scholars based in United States, United Kingdom and New Zealand. Frequent co-authors include Roger L. Albin, Mary Y. Heng, Thomas D. Petes, Sara J. Tallaksen‐Greene, Michael A. White, Kirupa Sathasivam, Gillian P. Bates, Richard L. M. Faull, Walker S. Jackson and Courtney J. Haycraft. Their work appears in journals such as Molecular and Cellular Biology, Human Molecular Genetics, Journal of Neuroscience, Proceedings of the National Academy of Sciences and Neurobiology of Disease.

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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