Mark A. Micale

1.3k total citations
32 papers, 689 citations indexed

About

Mark A. Micale is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Mark A. Micale has authored 32 papers receiving a total of 689 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 12 papers in Molecular Biology and 10 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Mark A. Micale's work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (7 papers) and Chromosomal and Genetic Variations (5 papers). Mark A. Micale is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (7 papers) and Chromosomal and Genetic Variations (5 papers). Mark A. Micale collaborates with scholars based in United States and United Kingdom. Mark A. Micale's co-authors include Sandra R. Wolman, Wael Sakr, Jill A. Macoska, Daniel W. Visscher, Isaac J. Powell, Stuart Schwartz, Jeffrey M. Conroy, Carol A. Crowe, Laurie A. Christ and Philip Benson and has published in prestigious journals such as SHILAP Revista de lepidopterología, JNCI Journal of the National Cancer Institute and The American Journal of Human Genetics.

In The Last Decade

Mark A. Micale

29 papers receiving 669 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 A. Micale United States 14 259 248 246 197 150 32 689
David J. McBride United Kingdom 9 343 1.3× 118 0.5× 306 1.2× 284 1.4× 151 1.0× 12 835
A. W. G. B. SMEETS Netherlands 12 261 1.0× 101 0.4× 142 0.6× 175 0.9× 89 0.6× 15 660
JDA Delhanty United Kingdom 17 285 1.1× 75 0.3× 399 1.6× 139 0.7× 324 2.2× 30 1.2k
John H. Proffitt United States 15 444 1.7× 110 0.4× 110 0.4× 93 0.5× 447 3.0× 17 1.1k
P. J. Fialkow United States 8 265 1.0× 64 0.3× 178 0.7× 182 0.9× 98 0.7× 10 734
Antonella Zagaria Italy 23 504 1.9× 57 0.2× 117 0.5× 242 1.2× 146 1.0× 80 1.2k
Marie‐Josée Le Bris France 18 420 1.6× 36 0.1× 220 0.9× 87 0.4× 78 0.5× 55 986
A Butturini United States 15 470 1.8× 55 0.2× 157 0.6× 108 0.5× 50 0.3× 41 1.1k
A. David B. Webster United Kingdom 18 242 0.9× 164 0.7× 295 1.2× 77 0.4× 83 0.6× 20 1.0k
Charlotte Jin Sweden 22 654 2.5× 44 0.2× 381 1.5× 201 1.0× 104 0.7× 43 1.1k

Countries citing papers authored by Mark A. Micale

Since Specialization
Citations

This map shows the geographic impact of Mark A. Micale'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. Micale 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. Micale more than expected).

Fields of papers citing papers by Mark A. Micale

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of Mark A. Micale. A scholar is included among the top collaborators of Mark A. Micale 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. Micale. Mark A. Micale 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.
Kennedy, Ann R., Kanika Arora, Harry Zhang, et al.. (2025). Varieties of altered TFE3 can occur in MiT-family-related renal cell carcinomas. International Urology and Nephrology. 57(8). 2425–2433.
2.
Micale, Mark A., et al.. (2019). Occult subtotal cleft of the secondary palate with VPI associated to 8q22.2 deletion. International Journal of Pediatric Otorhinolaryngology. 124. 54–58. 1 indexed citations
3.
4.
5.
Ysunza, Antonio, et al.. (2014). 22q11.2 deletion detected by endoscopic observation of pharyngeal pulsations in a child with submucous cleft palate and persistent velopharyngeal insufficiency. International Journal of Pediatric Otorhinolaryngology. 78(10). 1789–1794. 10 indexed citations
6.
7.
Shah, Priyanka A., et al.. (2013). Potential role of biofilms in deep cervical abscess. International Journal of Pediatric Otorhinolaryngology. 78(1). 10–13. 18 indexed citations
8.
Muslimani, Alaa, et al.. (2013). Pulmonary Infiltrates in Acute Myeloid Leukemia During Induction Treatment. American Journal of Clinical Oncology. 37(4). 377–383. 5 indexed citations
9.
Bhagavathi, Sharathkumar, et al.. (2009). Primary Bone Diffuse Large B-cell Lymphoma. The American Journal of Surgical Pathology. 33(10). 1463–1469. 27 indexed citations
10.
Micale, Mark A., et al.. (2007). Malignant blue nevus with lymph node metastases. Journal of Cutaneous Pathology. 35(7). 651–657. 16 indexed citations
11.
Micale, Mark A., et al.. (2007). Mosaic variegated aneuploidy without microcephaly: Implications for cytogenetic diagnosis. American Journal of Medical Genetics Part A. 143A(16). 1890–1893. 13 indexed citations
12.
Christ, Laurie A., Carol A. Crowe, Mark A. Micale, Jeffrey M. Conroy, & Stuart Schwartz. (1999). Chromosome Breakage Hotspots and Delineation of the Critical Region for the 9p-Deletion Syndrome. The American Journal of Human Genetics. 65(5). 1387–1395. 74 indexed citations
13.
Micale, Mark A., Diana Wolff, Lois H. Dickerman, et al.. (1996). CYTOGENETIC AND MOLECULAR GENETIC CHARACTERIZATION OF TRISOMY 20 MOSAICISM IN FETAL BLOOD AND TISSUES. Prenatal Diagnosis. 16(10). 893–897. 13 indexed citations
14.
Micale, Mark A., et al.. (1995). Parental origin of de novo chromosome 9 deletions in del(9p) syndrome. American Journal of Medical Genetics. 57(1). 79–81. 18 indexed citations
15.
Micale, Mark A., et al.. (1994). Chromosomal aneuploidy in proliferative breast disease. Human Pathology. 25(1). 29–35. 76 indexed citations
16.
Pretlow, T G, S R Wolman, Mark A. Micale, et al.. (1993). Xenografts of Primary Human Prostatic Carcinoma. JNCI Journal of the National Cancer Institute. 85(5). 394–398. 126 indexed citations
17.
Macoska, Jill A., Mark A. Micale, Wael Sakr, Philip Benson, & Sandra R. Wolman. (1993). Extensive genetic alterations in prostate cancer revealed by dual PCR and FISH analysis. Genes Chromosomes and Cancer. 8(2). 88–97. 69 indexed citations
18.
Micale, Mark A., et al.. (1993). Defining the extent and nature of cytogenetic events in prostatic adenocarcinoma: Paraffin FISH vs. metaphase analysis. Cancer Genetics and Cytogenetics. 69(1). 7–12. 50 indexed citations
19.
Micale, Mark A., et al.. (1992). Cytogenetics of primary prostatic adenocarcinoma. Cancer Genetics and Cytogenetics. 61(2). 165–173. 61 indexed citations
20.
Wolman, Sandra R., Jill A. Macoska, Mark A. Micale, & Wael Sakr. (1992). An Approach to Definition of Genetic Alterations in Prostate Cancer. Diagnostic Molecular Pathology. 1(1). 192–199. 26 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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