Michele Clemens

1.1k total citations
25 papers, 625 citations indexed

About

Michele Clemens is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Michele Clemens has authored 25 papers receiving a total of 625 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 12 papers in Pediatrics, Perinatology and Child Health and 10 papers in Surgery. Recurrent topics in Michele Clemens's work include Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (9 papers) and Cleft Lip and Palate Research (5 papers). Michele Clemens is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (9 papers) and Cleft Lip and Palate Research (5 papers). Michele Clemens collaborates with scholars based in United States, Australia and United Kingdom. Michele Clemens's co-authors include Elizabeth McPherson, Urvashi Surti, Angela E. Lin, Rosemarie Smith, Tom A. Maher, John B. Mulliken, Heather J. Stalker, Jeff M. Milunsky, Geping Zhao and Amy E. Roberts and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Journal of Oral and Maxillofacial Surgery.

In The Last Decade

Michele Clemens

25 papers receiving 610 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michele Clemens United States 15 394 298 157 123 69 25 625
R M Winter United Kingdom 14 402 1.0× 276 0.9× 94 0.6× 165 1.3× 57 0.8× 32 683
I D Young United Kingdom 17 350 0.9× 274 0.9× 151 1.0× 171 1.4× 28 0.4× 40 642
Carla Graziadio Brazil 14 236 0.6× 250 0.8× 176 1.1× 138 1.1× 46 0.7× 58 604
Constantinos Pángalos Greece 13 337 0.9× 220 0.7× 297 1.9× 41 0.3× 45 0.7× 38 643
Nataline B. Kardon United States 13 329 0.8× 232 0.8× 281 1.8× 66 0.5× 58 0.8× 26 640
Silvia Maitz Italy 17 319 0.8× 330 1.1× 123 0.8× 65 0.5× 15 0.2× 40 617
Susan J. Kirkpatrick United States 10 211 0.5× 154 0.5× 120 0.8× 122 1.0× 32 0.5× 13 430
M L Martínez-Frías Spain 10 152 0.4× 113 0.4× 103 0.7× 140 1.1× 23 0.3× 20 459
Daniela Bettio Italy 12 277 0.7× 169 0.6× 235 1.5× 49 0.4× 20 0.3× 35 535
Marc Le Lorc’h France 12 183 0.5× 168 0.6× 101 0.6× 171 1.4× 137 2.0× 19 476

Countries citing papers authored by Michele Clemens

Since Specialization
Citations

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

Fields of papers citing papers by Michele Clemens

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michele Clemens

This figure shows the co-authorship network connecting the top 25 collaborators of Michele Clemens. A scholar is included among the top collaborators of Michele Clemens 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 Michele Clemens. Michele Clemens 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.
Clemens, Michele, et al.. (2022). Antenatal Milk Expression as a Lactation Support Intervention for Parents of Infants With Severe Birth Defects. The Journal of Perinatal & Neonatal Nursing. 36(4). E25–E30. 7 indexed citations
2.
Hu, Jie, Urvashi Surti, Melanie Babcock, et al.. (2021). Reproductive outcomes in individuals with chromosomal reciprocal translocations. Genetics in Medicine. 23(9). 1753–1760. 25 indexed citations
3.
Saller, Devereux N., et al.. (2016). Genotype–phenotype correlation and pregnancy outcomes of partial trisomy 14q: A systematic review. American Journal of Medical Genetics Part A. 170(9). 2365–2371. 6 indexed citations
4.
Davis, S., Urvashi Surti, Stephen P. Emery, et al.. (2012). Application of chromosomal microarray in the evaluation of abnormal prenatal findings. Clinical Genetics. 84(1). 47–54. 32 indexed citations
5.
Sánchez-de-Toledo, Joan, Ricardo Muñoz, Richard A. Orr, et al.. (2011). Critical Congenital Heart Disease-Utility of Routine Screening for Chromosomal and Other Extracardiac Malformations. Congenital Heart Disease. 7(2). 145–150. 27 indexed citations
6.
Hendrix, Nancy W., Michele Clemens, Timothy Canavan, Urvashi Surti, & Aleksandar Rajkovic. (2011). Prenatally Diagnosed 17q12 Microdeletion Syndrome with a Novel Association with Congenital Diaphragmatic Hernia. Fetal Diagnosis and Therapy. 31(2). 129–133. 35 indexed citations
7.
Milunsky, Jeff M., Tom A. Maher, Geping Zhao, et al.. (2009). TFAP2A Mutations Result in Branchio-Oculo-Facial Syndrome. The American Journal of Human Genetics. 84(2). 301–301. 7 indexed citations
8.
Costello, Bernard J., Sean P. Edwards, & Michele Clemens. (2008). Fetal Diagnosis and Treatment of Craniomaxillofacial Anomalies. Journal of Oral and Maxillofacial Surgery. 66(10). 1985–1995. 15 indexed citations
9.
Milunsky, Jeff M., Tom A. Maher, Geping Zhao, et al.. (2008). TFAP2A Mutations Result in Branchio-Oculo-Facial Syndrome. The American Journal of Human Genetics. 82(5). 1171–1177. 161 indexed citations
10.
Prucka, Sandra K., et al.. (2004). Single umbilical artery: What does it mean for the fetus? A case-control analysis of pathologically ascertained cases. Genetics in Medicine. 6(1). 54–57. 36 indexed citations
11.
Wright, Tracy J., Michele Clemens, Oliver Quarrell, & Michael R. Altherr. (1998). Wolf-Hirschhorn and Pitt-Rogers-Danks syndromes caused by overlapping 4p deletions. American Journal of Medical Genetics. 75(4). 345–350. 31 indexed citations
12.
McPherson, Elizabeth, Michele Clemens, Lori Hoffner, & Urvashi Surti. (1998). Sacral tumors in Schinzel‐Giedion syndrome. American Journal of Medical Genetics. 79(1). 62–63. 1 indexed citations
13.
McPherson, Elizabeth & Michele Clemens. (1997). Bruck syndrome (osteogenesis imperfecta with congenital joint contractures): Review and report on the first North American case. American Journal of Medical Genetics. 70(1). 28–31. 29 indexed citations
14.
Clemens, Michele, et al.. (1997). Apparently balanced t(1;7)(q21.3;q34) in an infant with Coffin-Siris syndrome. American Journal of Medical Genetics. 71(4). 430–433. 19 indexed citations
15.
McPherson, Elizabeth & Michele Clemens. (1996). Cleft lip and palate, characteristic facial appearance, malrotation of the intestine, and lethal congenital heart disease in two sibs: A new autosomal recessive condition?. American Journal of Medical Genetics. 62(1). 58–60. 3 indexed citations
16.
Clemens, Michele, John T. Martsolf, John Rogers, et al.. (1996). Pitt-Rogers-Dank syndrome: The result of a 4p microdeletion. American Journal of Medical Genetics. 66(1). 95–100. 23 indexed citations
17.
Estop, A., Patricia Mowery‐Rushton, Kathleen Cieply, et al.. (1995). Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic features. Journal of Medical Genetics. 32(10). 819–822. 11 indexed citations
18.
McPherson, Elizabeth, Michele Clemens, Richard J. Gibbons, & Douglas R. Higgs. (1995). X‐linked α‐thalassemia/mental retardation (ATR‐X) syndrome: A new kindred with severe genital anomalies and mild hematologic expression. American Journal of Medical Genetics. 55(3). 302–306. 26 indexed citations
19.
Lin, Angela E., et al.. (1993). Further delineation of the Baller‐Gerold syndrome. American Journal of Medical Genetics. 45(4). 519–524. 17 indexed citations
20.
Lin, Angela E., Kenneth L. Garver, Michele Clemens, et al.. (1988). Interstitial and terminal deletions of the long arm of chromosome 4: Further delineation of phenotypes. American Journal of Medical Genetics. 31(3). 533–548. 87 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by R M Winter Breakdown of academic impact, for papers by I D Young Breakdown of academic impact, for papers by Carla Graziadio Breakdown of academic impact, for papers by Constantinos Pángalos Breakdown of academic impact, for papers by Nataline B. Kardon Breakdown of academic impact, for papers by Silvia Maitz Breakdown of academic impact, for papers by Susan J. Kirkpatrick Breakdown of academic impact, for papers by M L Martínez-Frías Breakdown of academic impact, for papers by Daniela Bettio Breakdown of academic impact, for papers by Marc Le Lorc’h
Rankless by CCL
2026