M Schmidt

881 total citations
28 papers, 559 citations indexed

About

M Schmidt is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, M Schmidt has authored 28 papers receiving a total of 559 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Genetics and 8 papers in Hematology. Recurrent topics in M Schmidt's work include Genetics and Neurodevelopmental Disorders (9 papers), Blood Coagulation and Thrombosis Mechanisms (6 papers) and RNA regulation and disease (5 papers). M Schmidt is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Blood Coagulation and Thrombosis Mechanisms (6 papers) and RNA regulation and disease (5 papers). M Schmidt collaborates with scholars based in United States, Germany and Canada. M Schmidt's co-authors include Eric M. Morrow, Qing Ouyang, Sofia B. Lizarraga, Jingyi Gong, W. Prohaska, K Kleesiek, Julie A. Kauer, Ece D. Gamsiz Uzun, Matthew F. Pescosolido and Thomas Brinkmann and has published in prestigious journals such as Journal of Biological Chemistry, Neuron and Blood.

In The Last Decade

M Schmidt

26 papers receiving 547 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M Schmidt United States 14 233 182 149 93 89 28 559
Ayse Bilge Ozel United States 14 245 1.1× 91 0.5× 131 0.9× 58 0.6× 33 0.4× 26 635
J. He China 14 222 1.0× 61 0.3× 238 1.6× 45 0.5× 221 2.5× 70 854
Ryan E. Lamont Canada 16 611 2.6× 50 0.3× 165 1.1× 148 1.6× 133 1.5× 35 850
Cheryl Y. Gregory United Kingdom 15 474 2.0× 365 2.0× 153 1.0× 60 0.6× 79 0.9× 25 935
Rachel Schot Netherlands 16 355 1.5× 29 0.2× 260 1.7× 107 1.2× 62 0.7× 35 686
Jorge Pinto‐Basto Portugal 11 204 0.9× 48 0.3× 120 0.8× 44 0.5× 115 1.3× 25 414
Rishard Salie Switzerland 11 233 1.0× 85 0.5× 25 0.2× 53 0.6× 177 2.0× 12 475
Dong-Hui Chen United States 9 370 1.6× 69 0.4× 83 0.6× 39 0.4× 277 3.1× 10 579
Seyedmehdi Shojaee United States 7 240 1.0× 62 0.3× 69 0.5× 47 0.5× 68 0.8× 13 508
Annick Blaise France 7 284 1.2× 162 0.9× 90 0.6× 15 0.2× 33 0.4× 7 618

Countries citing papers authored by M Schmidt

Since Specialization
Citations

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

Fields of papers citing papers by M Schmidt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M Schmidt. 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 M Schmidt. The network helps show where M Schmidt may publish in the future.

Co-authorship network of co-authors of M Schmidt

This figure shows the co-authorship network connecting the top 25 collaborators of M Schmidt. A scholar is included among the top collaborators of M Schmidt 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 M Schmidt. M Schmidt 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.
Ma, Li, et al.. (2024). GGA1 interacts with the endosomal Na+/H+ exchanger NHE6 governing localization to the endosome compartment. Journal of Biological Chemistry. 300(8). 107552–107552.
2.
Hollingsworth, Ethan W., et al.. (2023). Dysregulation of the chromatin environment leads to differential alternative splicing as a mechanism of disease in a human model of autism spectrum disorder. Human Molecular Genetics. 32(10). 1634–1646. 10 indexed citations
3.
Ouyang, Qing, M Schmidt, & Eric M. Morrow. (2023). Dynamic Measurement of Endosome-Lysosome Fusion in Neurons Using High-Content Imaging. Methods in molecular biology. 2683. 201–212.
4.
Fernandez, Marty A., Li Ma, Youjin Lee, et al.. (2022). Loss of endosomal exchanger NHE6 leads to pathological changes in tau in human neurons. Stem Cell Reports. 17(9). 2111–2126. 12 indexed citations
5.
Lizarraga, Sofia B., Li Ma, Laura I. van Dyck, et al.. (2021). Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies. Science Translational Medicine. 13(580). 20 indexed citations
6.
Ma, Li, M Schmidt, & Eric M. Morrow. (2021). Human iPSC lines from a Christianson syndrome patient with NHE6 W523X mutation, a biologically-related control, and CRISPR/Cas9 gene-corrected isogenic controls. Stem Cell Research. 54. 102435–102435. 3 indexed citations
7.
Ma, Li, et al.. (2021). Generation of pathogenic TPP1 mutations in human stem cells as a model for neuronal ceroid lipofuscinosis type 2 disease. Stem Cell Research. 53. 102323–102323. 6 indexed citations
8.
Ouyang, Qing, Brian C. Kavanaugh, Lena Joesch-Cohen, et al.. (2019). GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates. Human Genetics. 138(10). 1183–1200. 6 indexed citations
9.
Ouyang, Qing, et al.. (2019). Functional AssessmentIn Vivoof the Mouse Homolog of the Human Ala-9-Ser NHE6 Variant. eNeuro. 6(6). ENEURO.0046–19.2019. 5 indexed citations
10.
Pescosolido, Matthew F., Brian C. Kavanaugh, Nathalie Pochet, et al.. (2019). Complex Neurological Phenotype in Female Carriers of <b><i>NHE6</i></b> Mutations. PubMed. 5(2). 98–108. 8 indexed citations
11.
Xu, Meiyu, Qing Ouyang, Jingyi Gong, et al.. (2017). Mixed Neurodevelopmental and Neurodegenerative Pathology inNhe6-Null Mouse Model of Christianson Syndrome. eNeuro. 4(6). ENEURO.0388–17.2017. 19 indexed citations
12.
Schmidt, M, et al.. (2013). Pathway-PDT: a flexible pathway analysis tool for nuclear families. BMC Bioinformatics. 14(1). 267–267. 5 indexed citations
13.
Ouyang, Qing, Sofia B. Lizarraga, M Schmidt, et al.. (2013). Christianson Syndrome Protein NHE6 Modulates TrkB Endosomal Signaling Required for Neuronal Circuit Development. Neuron. 80(1). 97–112. 105 indexed citations
14.
Uzun, Ece D. Gamsiz, Qing Ouyang, M Schmidt, Shailender Nagpal, & Eric M. Morrow. (2011). Genome-wide transcriptome analysis in murine neural retina using high-throughput RNA sequencing. Genomics. 99(1). 44–51. 34 indexed citations
15.
16.
Arkin, Steven, Herbert Cooper, J. Hutter, et al.. (1998). Activated Recombinant Human Coagulation Factor VII Therapy for Intracranial Hemorrhage in Patients with Hemophilia A or B with Inhibitors. Pathophysiology of Haemostasis and Thrombosis. 28(2). 93–98. 60 indexed citations
17.
Prohaska, W., Hermann Mannebach, M Schmidt, U Gleichmann, & K Kleesiek. (1995). Evidence against heterozygous coagulation factor V 1691 G?A mutation with resistance to activated protein C being a risk factor for coronary artery disease and myocardial infarction. Journal of Molecular Medicine. 73(10). 521–4. 19 indexed citations
18.
Pötzsch, B., et al.. (1995). Acquired protein C dysfunction but not decreased activity of thrombomodulin is a possible marker of thrombophilia in patients with lupus anticoagulant.. PubMed. 125(1). 56–65. 24 indexed citations
19.
Schmidt, M, et al.. (1994). Recombinant activated factor VII (rFVIIa) therapy for intracranial hemorrhage in hemophilia a patients with inhibitors. American Journal of Hematology. 47(1). 36–40. 46 indexed citations
20.
Schmidt, M, et al.. (1991). Anti-Xa clotting activities in different hepatic-triglyceride lipase preparations from post-heparin plasma. Thrombosis Research. 63(5). 503–508. 1 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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