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M. Risinger · SciRah

Researcher profile · Semantic Scholar

M. Risinger

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M. Risinger — researcher profile on SciRah

h-index: 21
Works: 57
Citations: 1,610

Most-cited papers

Sites of Regulated Phosphorylation that Control K-Cl Cotransporter Activity
Jesse Rinehart, Y. Maksimova, J. Tanis, K. Stone +11 more
2009Cell309 citations Open access
Semantic Scholar
Enhanced Tumor Formation in Mice Heterozygous for Blm Mutation
K. Goss, M. Risinger, Jennifer J. Kordich, M. Sanz +6 more
2002Science224 citations
Semantic Scholar
Red Cell Membrane Disorders: Structure meets Function.
M. Risinger, T. Kalfa
2020Blood115 citations Open access
Semantic Scholar
UV-induced hyperphosphorylation of replication protein a depends on DNA replication and expression of ATM protein.
G. Oakley, L. Loberg, Jia-Qin Yao, M. Risinger +6 more
2001Molecular Biology of the Cell100 citations Open access
Semantic Scholar
Studies on proteins that co-purify with smooth muscle vinculin: identification of immunologically related species in focal adhesions of nonmuscle and Z-lines of muscle cells
J. Wilkins, M. Risinger, Shin Lin
1986Journal of Cell Biology83 citations Open access
Semantic Scholar
Crosslinks and crosstalk: human cancer syndromes and DNA repair defects.
M. Risinger, J. Groden
2004Cancer Cell74 citations Open access
Semantic Scholar
Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis
O. Niss, S. Chonat, Neha Dagaonkar, M. Almansoori +7 more
2016Blood Cells, Molecules & Diseases73 citations Open access
Semantic Scholar
An Erythropoietin Fusion Protein Comprised of Identical Repeating Domains Exhibits Enhanced Biological Properties*
A. Sytkowski, E. Lunn, M. Risinger, K. L. Davis
1999Journal of Biological Chemistry62 citations Open access
Semantic Scholar
Inhibition of Band 3 tyrosine phosphorylation: a new mechanism for treatment of sickle cell disease
Panae Noomuna, M. Risinger, Sitong Zhou, K. Seu +9 more
2020British Journal of Haematology58 citations Open access
Semantic Scholar
The Spectrum of SPTA1-Associated Hereditary Spherocytosis
S. Chonat, M. Risinger, Haripriya Sakthivel, O. Niss +13 more
2019Frontiers in Physiology58 citations Open access
Semantic Scholar
Human erythrocyte protein 4.2, a high copy number membrane protein, is N-myristylated.
M. Risinger, E. Dotimas, Carl M. Cohen
1992Journal of Biological Chemistry42 citations Open access
Semantic Scholar
Macrophage Apoptosis by Anthrax Lethal Factor Through p 38 MAP Kinase Inhibition
K. Goss, M. Risinger, Jennifer J. Kordich, M. Sanz +6 more
200239 citations
Semantic Scholar
The dynamic life histories of intercellular membrane junctions
W. J. Larsen, M. Risinger
198539 citations
Semantic Scholar
Cytokinesis failure in RhoA-deficient mouse erythroblasts involves actomyosin and midbody dysregulation and triggers p53 activation.
Diamantis G. Konstantinidis, Katie M Giger, M. Risinger, S. Pushkaran +8 more
2015Blood36 citations Open access
Semantic Scholar
Interaction of filipin with junctional membrane at different stages of the junction's life history.
M. Risinger, W. J. Larsen
1983Tissue & Cell36 citations
Semantic Scholar
K-Cl Cotransporter Gene Expression during Human and Murine Erythroid Differentiation*
Dao Pan, T. Kalfa, Da-Ren Wang, M. Risinger +7 more
2011Journal of Biological Chemistry34 citations Open access
Semantic Scholar
Rare Hereditary Hemolytic Anemias: Diagnostic Approach and Considerations in Management.
M. Risinger, Myesa Emberesh, T. Kalfa
2019Hematology/Oncology Clinics of North America31 citations
Semantic Scholar
A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemia
S. Hayette, L. Morlé, M. Bozon, A. Ghanem +6 more
1995British Journal of Haematology28 citations
Semantic Scholar
Actin filament organization of the Dunning R3327 rat prostatic adenocarcinoma system: correlation with metastatic potential.
J. Zachary, G. Cleveland, L. Kwock, Tommy L. Lawrence +6 more
1986Cancer Research28 citations
Semantic Scholar
DEFINING A PHENOTYPE FOR RED CELL VOLUME REGULATION AND POTASSIUM CHLORIDE COTRANSPORT
Maa-Ohui Quarmyne, M. Risinger, Andrew Linkugel, Anna Frazier +1 more
2011Blood Cells, Molecules & Diseases22 citations Open access
Semantic Scholar
Urea stimulation of KCl cotransport induces abnormal volume reduction in sickle reticulocytes.
C. Joiner, R. Rettig, Maorong Jiang, M. Risinger +1 more
2007Blood21 citations Open access
Semantic Scholar
Endocytosis of cell-cell junctions and spontaneous cell disaggregation in a cultured human ovarian adenocarcinoma. (COLO 316).
M. Risinger, W. J. Larsen
1981Tissue & Cell21 citations
Semantic Scholar
Hereditary xerocytosis: Diagnostic considerations
M. Risinger, E. Glogowska, S. Chonat, Ke-Jian Zhang +5 more
2017American journal of hematology/oncology11 citations Open access
Semantic Scholar
Role of N-myristylation in targeting of band 4.2 (pallidin) in nonerythroid cells.
M. Risinger, Catherine Korsgren, Carl M. Cohen
1996Experimental Cell Research8 citations
Semantic Scholar
Peroxiredoxin II (PRDX2) Is a Novel Candidate Gene for Congenital Dyserythropoietic Anemia
Myesa Emberesh, Katie Giger Seu, Sana E. Emberesh, Lisa R. Trump +7 more
2018Blood7 citations
Semantic Scholar
Hemolytic anemia and macrothrombocytopenia: a lipid problem?
M. Risinger, Phyllis Kim, R. Rodriguez, Monica Narvaez Rivas +3 more
2023American journal of hematology/oncology6 citations Open access
Semantic Scholar
Corrigendum: The Spectrum of SPTA1-Associated Hereditary Spherocytosis
S. Chonat, M. Risinger, Haripriya Sakthivel, O. Niss +13 more
2019Frontiers in Physiology6 citations Open access
Semantic Scholar
Session 7
Z. Shen, J. Lozach, V. Cavalli, J. Rinehart +14 more
2009Molecular & Cellular Proteomics6 citations Open access
Semantic Scholar
Hereditary elliptocytosis-associated alpha-spectrin mutation p.L155dup as a modifier of sickle cell disease severity
M. Risinger, Georgios E Christakopoulos, Corinna L. Schultz, Patrick T. McGann +2 more
2018Pediatric Blood & Cancer5 citations Open access
Semantic Scholar
The Novel PIEZO1 Mutation p.L2023V Is Causal for Hereditary Xerocytosis Resulting in Delayed Channel Inactivation and a Dehydrated Red Blood Cell Phenotype
M. Risinger, E. Glogowska, A. Begtrup, Neha Dagaonkar +5 more
20144 citations
Semantic Scholar
The Spectrum of Alpha-Spectrin Associated Hereditary Spherocytosis
S. Chonat, M. Risinger, Neha Dagaonkar, Tamara Maghathe +6 more
20153 citations
Semantic Scholar
DEFINING A PHENOTYPE FOR RED CELL VOLUME REGULATION AND POTASSIUM CHLORIDE COTRANSPORT
Maa-Ohui Quarmyne, M. Risinger, Andrew Linkugel, Anna Frazier +2 more
20133 citations
Semantic Scholar
Compound heterozygosity for two novel mutations in the erythrocyte protein 4.2 gene causing spherocytosis in a Caucasian patient
Adrienne M. Hammill, M. Risinger, C. Joiner, M. Keddache +1 more
2011British Journal of Haematology3 citations Open access
Semantic Scholar
A Model for Protein-Protein Interactions Involved in the Linkage of the Actin Cytoskeleton to Transmembrane Receptors for Extracellular Matrix Proteins
Lin Shin, M. Risinger, J. A. Butler
19893 citations
Semantic Scholar
Advances on the genetic basis of red cell membrane disorders
M. Risinger, Wenying Zhang, T. Kalfa
2025Current opinion in hematology2 citations Open access
Semantic Scholar
Loss of ATG5 in Humans Causes Syndromic Congenital Dyserythropoietic Anemia with Impaired Mitophagy in Late Stages of Terminal Erythropoiesis
A. Ntoumaziou, Duc Nguyen, Yasmin Elgammal, Ammar Husami +10 more
2024Blood2 citations Open access
Semantic Scholar
Rapid degradation of protein tyrosine phosphatase 1B in sickle cells: Possible contribution to sickle cell membrane weakening
Panae Noomuna, J. Hausman, Ruhani Sansoya, T. Kalfa +2 more
2022The FASEB Journal2 citations Open access
Semantic Scholar
Evaluation of Phenotype-Genotype Correlation in Two Common PIEZO1 Mutations p.R2456H and p.L2495_E2495dup
M. Risinger, Vandy Black, L. Hsieh, R. Prins +9 more
2018Blood2 citations
Semantic Scholar
Clinical Application of Massively Parallel Sequencing in the Diagnosis of Hereditary Hemolytic and Dyserythropoietic Anemias
Harry Lesmana, Georgios E Christakopoulos, K. Seu, M. Risinger +4 more
20162 citations
Semantic Scholar
RGL2 Deficiency Impairs Human Erythropoiesis By Altering Terminal Erythroid Differentiation and Apoptosis.
Harry Lesmana, Georgios E Christakopoulos, M. Risinger, Haripriya Sakthivel +2 more
2017Blood1 citations Open access
Semantic Scholar
Next Generation Sequencing for Diagnostic Testing of Erythrocyte Cytoskeleton Disorders
T. Kalfa, M. Risinger, S. Pushkaran, P. Dexheimer +5 more
20121 citations
Semantic Scholar
recQ DNA Helicase Family in Genetic Stability
M. Risinger, J. Groden
20041 citations
Semantic Scholar
Cryohydrocytosis: When Cold Breaks the Membrane
A. Ntoumaziou, M. Risinger, Yasmin Elgammal, Wenying Zhang +2 more
2026American journal of hematology/oncology0 citations Open access
Semantic Scholar
Biomarkers of ineffective erythropoiesis in patients with sickle cell anemia, at baseline and while treated with hydroxyurea, in comparison to patients with other iron-loading red cell disorders
Yasmin Elgammal, Lubna Hamdan, M. Risinger, Diamantis Kostantinidis +7 more
2025Blood0 citations
Semantic Scholar
Erythroid-specific, inducible CDAN1∆/∆ mouse model phenocopies congenital dyserythropoietic anemia type-la
Corbin R Azucenas, Aikaterini Voulgaridou, Yasmin Elgammal, A. Ntoumaziou +6 more
2025Blood0 citations
Semantic Scholar
Hereditary spherocytic pyropoikilocytosis: Expanding the clinical and genetic spectrum of red blood cell membrane disorders
A. Ntoumaziou, Ammar Husami, M. Risinger, Yasmin Elgammal +5 more
2025Blood0 citations
Semantic Scholar
Transcriptomic analysis uncovers hidden intronic and synonymous pathogenic variants in red cell membrane disorders
Wenying Zhang, Yasmin Elgammal, Ammar Husami, Aikaterini Voulgaridou +9 more
2025Blood0 citations
Semantic Scholar
Congenital Dyserythropoietic Anemia Type II: An Update from the Congenital Dyseryhtropoietic Anemia Registry of North America (CDAR)
Yasmin Elgammal, M. Risinger, Ammar Husami, Joseph Walden +14 more
2023Blood0 citations Open access
Semantic Scholar
Role of Band 3 Tyrosine Phosphorylation in Causing the Vaso-Occlusive Events in Sickle Cell Disease
Panae Noomuna, M. Risinger, Sitong Zhou, K. Seu +9 more
2020Social Science Research Network0 citations
Semantic Scholar
INHERITED ANEMIAS Red cell membrane disorders: structure meets function
M. Risinger, T. Kalfa
20200 citations
Semantic Scholar

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