Mark J. Solloway

5.1k total citations
23 papers, 2.4k citations indexed

About

Mark J. Solloway is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Mark J. Solloway has authored 23 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 6 papers in Surgery and 6 papers in Genetics. Recurrent topics in Mark J. Solloway's work include Congenital heart defects research (8 papers), Developmental Biology and Gene Regulation (5 papers) and TGF-β signaling in diseases (4 papers). Mark J. Solloway is often cited by papers focused on Congenital heart defects research (8 papers), Developmental Biology and Gene Regulation (5 papers) and TGF-β signaling in diseases (4 papers). Mark J. Solloway collaborates with scholars based in United States, Australia and Brazil. Mark J. Solloway's co-authors include Elizabeth J. Robertson, Khanhky Phamluong, Andrew S. Peterson, Karen M. Lyons, Elizabeth K. Bikoff, Ethan Bier, V. François, Brigid L.M. Hogan, Andrew T. Dudley and Jason O’Neill and has published in prestigious journals such as Genes & Development, The Journal of Cell Biology and PLoS ONE.

In The Last Decade

Mark J. Solloway

23 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark J. Solloway United States 20 2.0k 566 352 285 252 23 2.4k
Daniel Dufort Canada 27 2.5k 1.3× 656 1.2× 467 1.3× 226 0.8× 236 0.9× 49 3.6k
Hiroki Kokubo Japan 26 1.7k 0.8× 397 0.7× 229 0.7× 147 0.5× 144 0.6× 46 2.2k
Karin Schuster-Gossler Germany 33 2.8k 1.4× 790 1.4× 366 1.0× 221 0.8× 199 0.8× 53 3.4k
Sigmar Stricker Germany 36 2.6k 1.3× 825 1.5× 259 0.7× 286 1.0× 126 0.5× 74 3.5k
Mark C. Hanks United States 15 1.9k 1.0× 532 0.9× 185 0.5× 189 0.7× 123 0.5× 18 2.5k
Sarah De Val United Kingdom 20 2.6k 1.3× 493 0.9× 265 0.8× 551 1.9× 285 1.1× 34 3.1k
David J. Goldhamer United States 32 2.6k 1.3× 630 1.1× 570 1.6× 233 0.8× 99 0.4× 57 3.6k
David E. Clouthier United States 31 2.5k 1.2× 1.2k 2.1× 502 1.4× 206 0.7× 273 1.1× 56 3.9k
Aimée Zúñiga Switzerland 25 2.9k 1.5× 833 1.5× 245 0.7× 389 1.4× 97 0.4× 45 3.9k
Ingolf Bach United States 29 2.4k 1.2× 900 1.6× 309 0.9× 351 1.2× 86 0.3× 48 3.1k

Countries citing papers authored by Mark J. Solloway

Since Specialization
Citations

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

Fields of papers citing papers by Mark J. Solloway

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark J. Solloway

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

All Works

20 of 20 papers shown
1.
Wykoff, Charles C., Vrinda Hershberger, David Eichenbaum, et al.. (2021). Inhibition of Complement Factor 3 in Geographic Atrophy with NGM621: Phase 1 Dose-Escalation Study Results. American Journal of Ophthalmology. 235. 131–142. 20 indexed citations
2.
Smith, Derek K., Lance Kates, Steffen Durinck, et al.. (2020). Elevated Serum Amino Acids Induce a Subpopulation of Alpha Cells to Initiate Pancreatic Neuroendocrine Tumor Formation. Cell Reports Medicine. 1(5). 100058–100058. 17 indexed citations
3.
Solloway, Mark J., Azadeh Madjidi, Chunyan Gu, et al.. (2015). Glucagon Couples Hepatic Amino Acid Catabolism to mTOR-Dependent Regulation of α-Cell Mass. Cell Reports. 12(3). 495–510. 144 indexed citations
4.
Phamluong, Khanhky, Wei Lin, Kai Barck, et al.. (2012). Chondroitin sulfate synthase 1 (Chsy1) is required for bone development and digit patterning. Developmental Biology. 363(2). 413–425. 67 indexed citations
5.
Koss, Matthew, Alexandre Bolze, Andrea Brendolan, et al.. (2012). Congenital Asplenia in Mice and Humans with Mutations in a Pbx/Nkx2-5/p15 Module. Developmental Cell. 22(5). 913–926. 52 indexed citations
6.
Phamluong, Khanhky, Li Li, Mei Sun, et al.. (2011). Global defects in collagen secretion in a Mia3/TANGO1 knockout mouse. The Journal of Cell Biology. 193(5). 935–951. 148 indexed citations
7.
Gong, Yan, Eric Bourhis, Cecilia Chiu, et al.. (2010). Wnt Isoform-Specific Interactions with Coreceptor Specify Inhibition or Potentiation of Signaling by LRP6 Antibodies. PLoS ONE. 5(9). e12682–e12682. 173 indexed citations
8.
Zoltewicz, J. Susie, Amir M. Ashique, Stacy Taylor, et al.. (2009). Wnt Signaling Is Regulated by Endoplasmic Reticulum Retention. PLoS ONE. 4(7). e6191–e6191. 39 indexed citations
9.
Endoh‐Yamagami, Setsu, Marie Evangelista, Xiaohui Wen, et al.. (2009). The Mammalian Cos2 Homolog Kif7 Plays an Essential Role in Modulating Hh Signal Transduction during Development. Current Biology. 19(15). 1320–1326. 186 indexed citations
10.
Ashique, Amir M., Youngshik Choe, Mattias Karlén, et al.. (2009). The Rfx4 Transcription Factor Modulates Shh Signaling by Regional Control of Ciliogenesis. Science Signaling. 2(95). ra70–ra70. 64 indexed citations
11.
Furtado, Milena B., Mark J. Solloway, Vanessa Jones, et al.. (2008). BMP/SMAD1 signaling sets a threshold for the left/right pathway in lateral plate mesoderm and limits availability of SMAD4. Genes & Development. 22(21). 3037–3049. 57 indexed citations
12.
Preis, Jost I., et al.. (2006). Generation of conditionalCited2 null alleles. genesis. 44(12). 579–583. 20 indexed citations
13.
Elliott, David A., Mark J. Solloway, Christine Biben, et al.. (2006). A tyrosine-rich domain within homeodomain transcription factor Nkx2-5 is an essential element in the early cardiac transcriptional regulatory machinery. Development. 133(7). 1311–1322. 20 indexed citations
14.
Stennard, Fiona A., Mauro W. Costa, Donna Lai, et al.. (2005). Murine T-box transcription factor Tbx20 acts as a repressor during heart development, and is essential for adult heart integrity, function and adaptation. Development. 132(10). 2451–2462. 171 indexed citations
15.
Solloway, Mark J.. (2003). Molecular pathways in myocardial development: a stem cell perspective. Cardiovascular Research. 58(2). 264–277. 71 indexed citations
16.
Harvey, Richard P., David A. Elliott, Christine Biben, et al.. (2002). Homeodomain Factor Nkx2-5 in Heart Development and Disease. Cold Spring Harbor Symposia on Quantitative Biology. 67(0). 107–114. 55 indexed citations
17.
Robertson, Elizabeth J., et al.. (2001). Bmp6 and Bmp7 Are Required for Cushion Formation and Septation in the Developing Mouse Heart. Developmental Biology. 235(2). 449–466. 174 indexed citations
18.
Solloway, Mark J. & Elizabeth J. Robertson. (1999). Early embryonic lethality in Bmp5;Bmp7 double mutant mice suggests functional redundancy within the 60A subgroup. Development. 126(8). 1753–1768. 277 indexed citations
19.
Solloway, Mark J., Andrew T. Dudley, Elizabeth K. Bikoff, et al.. (1998). Mice lackingBmp6 function. Developmental Genetics. 22(4). 321–339. 293 indexed citations
20.
François, V., et al.. (1994). Dorsal-ventral patterning of the Drosophila embryo depends on a putative negative growth factor encoded by the short gastrulation gene.. Genes & Development. 8(21). 2602–2616. 262 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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