Jeanne Meck

2.7k total citations
57 papers, 1.5k citations indexed

About

Jeanne Meck is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jeanne Meck has authored 57 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 20 papers in Molecular Biology and 20 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jeanne Meck's work include Genomic variations and chromosomal abnormalities (28 papers), Prenatal Screening and Diagnostics (20 papers) and Genomics and Rare Diseases (6 papers). Jeanne Meck is often cited by papers focused on Genomic variations and chromosomal abnormalities (28 papers), Prenatal Screening and Diagnostics (20 papers) and Genomics and Rare Diseases (6 papers). Jeanne Meck collaborates with scholars based in United States, Saudi Arabia and South Sudan. Jeanne Meck's co-authors include Bassem R. Haddad, Michael D. Johnson, Chad J. Creighton, James M. Rae, Helga V. Toriello, Chahira Kozma, Jan Blancato, Swaroop Aradhya, Kenneth N. Rosenbaum and Daniel Pineda‐Alvarez and has published in prestigious journals such as Blood, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

In The Last Decade

Jeanne Meck

56 papers receiving 1.4k citations

Peers

Countries citing papers authored by Jeanne Meck

Since Specialization

Citations

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

Fields of papers citing papers by Jeanne Meck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jeanne Meck

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy number variants 2019 ·Genetics in Medicine ·Tracy Brandt, Laura M. Sack, Dolores Arjona, (unknown), Hui Mei, Hong Cui, Hua Gao, Lora Jh Bean, Arunkanth Ankala, Daniela del Gaudio, Amy Knight Johnson, Lisa M. Vincent, (unknown), (unknown), Gabriele Richard, Jeanne Meck	88
2	Diagnostic cytogenetic testing following positive noninvasive prenatal screening results: a clinical laboratory practice resource of the American College of Medical Genetics and Genomics (ACMG) 2017 ·Genetics in Medicine ·Athena M. Cherry, Yassmine Akkari, (unknown), Hutton M. Kearney, Nancy C. Rose, Sarah T. South, James Tepperberg, Jeanne Meck	29
3	Noninvasive prenatal screening for aneuploidy: positive predictive values based on cytogenetic findings 2015 ·American Journal of Obstetrics and Gynecology ·Jeanne Meck, (unknown), Ludmila Matyakhina, Ayala Aviram, Carolyn Trunca, Daniel Pineda‐Alvarez, Swaroop Aradhya, Rachel T. Klein, Athena M. Cherry	41
4	Assessing copy number from exome sequencing and exome array CGH based on CNV spectrum in a large clinical cohort 2014 ·Genetics in Medicine ·Kyle Retterer, Julie Scuffins, Daniel Schmidt, Rachel Lewis, Daniel Pineda‐Alvarez, Amanda Stafford, Lindsay Schmidt, (unknown), Federica Gibellini, (unknown), A. D. Blair, Sherri J. Bale, Ludmila Matyakhina, Jeanne Meck, Swaroop Aradhya, Eden Haverfield	86
5	A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity 2012 ·Genetics in Medicine ·(unknown), Swaroop Aradhya, Jeanne Meck, George E. Tiller, (unknown), Harold N. Bass	16
6	Histiocytic sarcoma transdifferentiated from follicular lymphoma presenting as a cutaneous tumor 2011 ·Journal of Cutaneous Pathology ·Weifen Zeng, Jeanne Meck, Bruce D. Cheson, Metin Özdemirli	21
7	Long-term persistence of nonpathogenic clonal chromosome abnormalities in donor hematopoietic cells after allogeneic stem cell transplantation 2009 ·Cancer Genetics and Cytogenetics ·Gulsun Erdag, Jeanne Meck, Aurelia Meloni‐Ehrig, Ludmila Matyakhina, (unknown), Ramaprasad Srinivasan, Philip N. Mowrey, (unknown), (unknown), Richard Childs	3
8	Patient decisions regarding prenatal aneuploid fluorescencein situhybridization results 2007 ·International Journal of Gynecology & Obstetrics ·(unknown), Helain J. Landy, Jeanne Meck	5
9	MDA-MB-435 cells are derived from M14 Melanoma cells––a loss for breast cancer, but a boon for melanoma research 2006 ·Breast Cancer Research and Treatment ·James M. Rae, Chad J. Creighton, Jeanne Meck, Bassem R. Haddad, Michael D. Johnson	307
10	Segregation of a t(1;3) translocation in multiple affected family members with both types of adjacent‐1 segregants 2003 ·American Journal of Medical Genetics Part A ·Chahira Kozma, Anne Slavotinek, Jeanne Meck	22
11	CD5‐Negative, CD10‐Negative small B‐cell leukemia: Variant of chronic lymphocytic leukemia or a distinct entity? 2002 ·American Journal of Hematology ·Salwa Sheikh, Bhaskar Kallakury, (unknown), Jeanne Meck, Dan P. Hartmann, Adam Bagg	19
12	Trisomy 7p resulting from 7p15;9p24 translocation: Report of a new case and review of associated medical complications 2000 ·American Journal of Medical Genetics ·Chahira Kozma, Bassem R. Haddad, Jeanne Meck	25
13	Risk of abnormal triple screen for Down syndrome is significantly higher in patients with female fetuses 1999 ·Prenatal Diagnosis ·Catherine Y. Spong, Alessandro Ghidini, (unknown), Jeanne Meck, (unknown), John C. Pezzullo	20
14	Identification of de novo chromosomal markers and derivatives by spectral karyotyping 1998 ·Human Genetics ·Bassem R. Haddad, Evelin Schröck, Jeanne Meck, Janet M. Cowan, Hannah Young, M.A. Ferguson‐Smith, Stanislas du Manoir, Thomas Ried	55
15	PRENATAL DETECTION OFDE NOVO INVERSION OF CHROMOSOME (2) (p13q11.2) AND POSTNATAL FOLLOW-UP 1996 ·Prenatal Diagnosis ·Chahira Kozma, (unknown), Jeanne Meck	3
16	PRENATAL DIAGNOSIS OF AN INFANT WITH MOSAIC TRISOMY 16 OF PATERNAL ORIGIN 1996 ·Prenatal Diagnosis ·(unknown), David M. Sherer, Susan L. Christian, (unknown), David H. Ledbetter, Carolyn M. Salafia, Jeanne Meck	14
17	Keratinocytes Immortalized by Human Papillomavirus-18 Exhibit Alterations Dependent upon Host Genetic Background and Complexity of Viral Genes Transfected 1994 ·Pathobiology ·(unknown), (unknown), Jeanne Meck, (unknown)	4
18	Cotransfection of HPV-18 and v-fos DNA Induces Tumorigenicity of Primary Human Keratinocytes 1993 ·Virology ·(unknown), Jeanne Meck, David A. Greenhalgh, Richard Schlegel	39
19	Prenatal diagnosis of tetrasomy 12p by in situ hybridization: Varying levels of mosaicism in different fetal tissues 1992 ·Prenatal Diagnosis ·Jan Blancato, (unknown), Julia B. George, Jacqueline M. Katz, Jeanne Meck	26
20	Familial Wolf-Hirschhorn syndrome associated with Rieger anomaly of the eye 1990 ·Ophthalmic Paediatrics and Genetics ·Chahira Kozma, (unknown), Jeanne Meck, Elias I. Traboulsi, (unknown)	10

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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