Simon E. Alfred

3.7k total citations
9 papers, 568 citations indexed

About

Simon E. Alfred is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Simon E. Alfred has authored 9 papers receiving a total of 568 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Cognitive Neuroscience. Recurrent topics in Simon E. Alfred's work include Photosynthetic Processes and Mechanisms (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Congenital heart defects research (2 papers). Simon E. Alfred is often cited by papers focused on Photosynthetic Processes and Mechanisms (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Congenital heart defects research (2 papers). Simon E. Alfred collaborates with scholars based in Canada, United States and Austria. Simon E. Alfred's co-authors include Stephen W. Scherer, Gevork N. Mnatzakanian, Hannes Lohi, Iulia Munteanu, Berge A. Minassian, Takahiro Yamada, N. Carolyn Schanen, Michael J. Friez, Julie R. Jones and John B. Vincent and has published in prestigious journals such as Nature Genetics, Biological Psychiatry and The Plant Journal.

In The Last Decade

Simon E. Alfred

9 papers receiving 561 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Simon E. Alfred Canada	8	424	294	179	151	49	9	568
Debashish U. Menon United States	12	272 0.6×	201 0.7×	105 0.6×	71 0.5×	35 0.7×	15	375
Xinlei Li China	8	199 0.5×	104 0.4×	76 0.4×	60 0.4×	48 1.0×	21	341
Nir Oksenberg United States	9	334 0.8×	160 0.5×	40 0.2×	78 0.5×	14 0.3×	12	462
Sailaja Peddada United States	5	431 1.0×	394 1.3×	29 0.2×	187 1.2×	26 0.5×	7	569
Laura M. Lombardi United States	9	226 0.5×	176 0.6×	61 0.3×	91 0.6×	14 0.3×	11	334
Gavin J Sutton Australia	4	340 0.8×	186 0.6×	30 0.2×	48 0.3×	34 0.7×	7	434
Jonathon Keeney United States	8	192 0.5×	145 0.5×	56 0.3×	53 0.4×	22 0.4×	12	307
Doris Wöhrle Germany	6	425 1.0×	492 1.7×	47 0.3×	193 1.3×	14 0.3×	8	619
Enrico Cannavò Germany	5	315 0.7×	144 0.5×	65 0.4×	21 0.1×	28 0.6×	5	392
Daniel M. Bader Germany	6	169 0.4×	119 0.4×	15 0.1×	48 0.3×	28 0.6×	6	294

Countries citing papers authored by Simon E. Alfred

Since Specialization

Citations

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

Fields of papers citing papers by Simon E. Alfred

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Simon E. Alfred. 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 Simon E. Alfred. The network helps show where Simon E. Alfred may publish in the future.

Co-authorship network of co-authors of Simon E. Alfred

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

All Works

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9 of 9 papers shown

Dejonghe, Wim, Aditya S. Vaidya, Simon E. Alfred, & Sean R. Cutler. (2021). In Planta Labeling Using a Clickable ER-Disrupting Probe Suggests a Role for Oleosins in Arabidopsis Seedling ER Integrity. ACS Chemical Biology. 16(11). 2151–2157. 5 indexed citations

Merico, Daniele, Gregory Costain, Simon E. Alfred, et al.. (2014). Copy Number Variable MicroRNAs in Schizophrenia and Their Neurodevelopmental Gene Targets. Biological Psychiatry. 77(2). 158–166. 52 indexed citations

Merico, Daniele, et al.. (2014). MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome. Frontiers in Neurology. 5. 238–238. 38 indexed citations

Chatfield, Steven P., et al.. (2012). Incipient stem cell niche conversion in tissue culture: using a systems approach to probe early events in WUSCHEL‐dependent conversion of lateral root primordia into shoot meristems. The Plant Journal. 73(5). 798–813. 87 indexed citations

Alfred, Simon E., Anuradha Surendra, X. Chris Le, et al.. (2012). A phenotypic screening platform to identify small molecule modulators of Chlamydomonas reinhardtiigrowth, motility and photosynthesis. Genome biology. 13(11). R105–R105. 15 indexed citations

Vincent, John B., Abdul Noor, Christian Windpassinger, et al.. (2008). Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close toSH3TC2,ADRB2, andHTR4on 5q, and within the desmocollin gene cluster on 18q. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(6). 817–826. 11 indexed citations

Zhao, Yang, Tsz-fung F. Chow, Simon E. Alfred, et al.. (2007). Chemical genetic interrogation of natural variation uncovers a molecule that is glycoactivated. Nature Chemical Biology. 3(11). 716–721. 90 indexed citations

Noor, Abdul, Gevork N. Mnatzakanian, Simon E. Alfred, et al.. (2006). Sequence variants within exon 1 of MECP2 occur in females with mental retardation. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(3). 355–360. 19 indexed citations

Mnatzakanian, Gevork N., Hannes Lohi, Iulia Munteanu, et al.. (2004). A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome. Nature Genetics. 36(4). 339–341. 251 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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