Mark A. Durham

439 total citations
14 papers, 270 citations indexed

About

Mark A. Durham is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Mark A. Durham has authored 14 papers receiving a total of 270 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Surgery. Recurrent topics in Mark A. Durham's work include Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and Tracheal and airway disorders (3 papers). Mark A. Durham is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and Tracheal and airway disorders (3 papers). Mark A. Durham collaborates with scholars based in United States, France and Poland. Mark A. Durham's co-authors include Donna M. Martin, Elizabeth A. Hurd, Dante Francomano, Adam Stein, Amandine Gasc, Benjamin L. Gottesman, Bryan C. Pijanowski, Elyse Reamer, Jinha Jung and Huda Y. Zoghbi and has published in prestigious journals such as Neuron, Developmental Cell and Human Molecular Genetics.

In The Last Decade

Mark A. Durham

14 papers receiving 265 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Mark A. Durham United States	9	149	91	40	37	34	14	270
Taro Kitazawa Japan	12	263 1.8×	93 1.0×	47 1.2×	18 0.5×	20 0.6×	29	449
Mou Cao United States	8	142 1.0×	40 0.4×	12 0.3×	60 1.6×	16 0.5×	10	282
Joseph J. Lancman United States	14	334 2.2×	119 1.3×	10 0.3×	46 1.2×	31 0.9×	16	507
Elliot Sollis Netherlands	7	147 1.0×	113 1.2×	36 0.9×	10 0.3×	8 0.2×	9	240
Alberto Roselló‐Díez Australia	10	304 2.0×	74 0.8×	7 0.2×	26 0.7×	7 0.2×	19	402
Silvia Naranjo Spain	11	477 3.2×	153 1.7×	12 0.3×	11 0.3×	17 0.5×	23	649
Uirá Souto Melo Brazil	10	261 1.8×	119 1.3×	35 0.9×	13 0.4×	3 0.1×	20	387
Mark Reijnen Netherlands	7	384 2.6×	172 1.9×	24 0.6×	30 0.8×	8 0.2×	7	483
Michael Getman United States	11	138 0.9×	81 0.9×	30 0.8×	4 0.1×	13 0.4×	22	295
Alisa Poh Australia	6	280 1.9×	53 0.6×	17 0.4×	23 0.6×	21 0.6×	6	393

Countries citing papers authored by Mark A. Durham

Since Specialization

Citations

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

Fields of papers citing papers by Mark A. Durham

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark A. Durham. 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 Mark A. Durham. The network helps show where Mark A. Durham may publish in the future.

Co-authorship network of co-authors of Mark A. Durham

This figure shows the co-authorship network connecting the top 25 collaborators of Mark A. Durham. A scholar is included among the top collaborators of Mark A. Durham 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 Mark A. Durham. Mark A. Durham is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Butts, Jessica C., Mark A. Durham, Ryan S. Dhindsa, et al.. (2024). A single-cell transcriptomic map of the developing Atoh1 lineage identifies neural fate decisions and neuronal diversity in the hindbrain. Developmental Cell. 59(16). 2171–2188.e7. 7 indexed citations

Bajikar, Sameer S., Jian Zhou, Ryan O’Hara, et al.. (2024). Acute MeCP2 loss in adult mice reveals transcriptional and chromatin changes that precede neurological dysfunction and inform pathogenesis. Neuron. 113(3). 380–395.e8. 7 indexed citations

Butts, Jessica C., et al.. (2023). Atoh1 drives the heterogeneity of the pontine nuclei neurons and promotes their differentiation. Science Advances. 9(26). eadg1671–eadg1671. 3 indexed citations

Bajikar, Sameer S., Ashley G. Anderson, Jian Zhou, et al.. (2023). MeCP2 regulates Gdf11, a dosage-sensitive gene critical for neurological function. eLife. 12. 9 indexed citations

Durham, Mark A., Larissa Nitschke, Amanda M Brown, et al.. (2022). Disruption of the ATXN1-CIC complex reveals the role of additional nuclear ATXN1 interactors in spinocerebellar ataxia type 1. Neuron. 111(4). 481–492.e8. 19 indexed citations

Durham, Mark A., et al.. (2022). Critical care paramedics’ experiences of performing an emergency scalpel cricothyroidotomy: a qualitative study. British Paramedic Journal. 7(1). 3–8. 1 indexed citations

Lavery, Laura A., Kerstin Ure, Ying‐Wooi Wan, et al.. (2020). Losing Dnmt3a dependent methylation in inhibitory neurons impairs neural function by a mechanism impacting Rett syndrome. eLife. 9. 36 indexed citations

Gasc, Amandine, Benjamin L. Gottesman, Dante Francomano, et al.. (2018). Soundscapes reveal disturbance impacts: biophonic response to wildfire in the Sonoran Desert Sky Islands. Landscape Ecology. 33(8). 1399–1415. 46 indexed citations

Hurd, Elizabeth A., et al.. (2014). The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development. Developmental Dynamics. 243(9). 1055–1066. 40 indexed citations

10.

Seeley, Andrea, et al.. (2014). Macrocerebellum, epilepsy, intellectual disability, and gut malrotation in a child with a 16q24.1–q24.2 contiguous gene deletion. American Journal of Medical Genetics Part A. 164(8). 2062–2068. 9 indexed citations

11.

Layman, Wanda S., Elizabeth A. Hurd, Mark A. Durham, et al.. (2013). CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome. Human Molecular Genetics. 23(2). 434–448. 53 indexed citations

12.

Marks, Daniel L., Nathan Hagen, Mark A. Durham, & David J. Brady. (2013). Wide-field compact catadioptric telescope spanning 07–14 μm wavelengths. Applied Optics. 52(18). 4334–4334. 4 indexed citations

13.

Bedoyan, Jirair K., Weiping Peng, Yongsheng Bai, et al.. (2012). Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder. Journal of Medical Genetics. 49(5). 332–340. 14 indexed citations

14.

Anton, Peter A., Stephan R. Targan, Steven R. Vigna, et al.. (1988). Enhanced neutrophil chemiluminescence in familial mediterranean fever. Journal of Clinical Immunology. 8(2). 148–156. 22 indexed citations

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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