Hillary F. Massa

6.7k total citations · 1 hit paper
27 papers, 3.9k citations indexed

About

Hillary F. Massa is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Hillary F. Massa has authored 27 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Genetics and 6 papers in Plant Science. Recurrent topics in Hillary F. Massa's work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (5 papers) and RNA modifications and cancer (3 papers). Hillary F. Massa is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (5 papers) and RNA modifications and cancer (3 papers). Hillary F. Massa collaborates with scholars based in United States, France and Sweden. Hillary F. Massa's co-authors include Barbara J. Trask, Janet M. Young, Evan E. Eichler, Jeffrey A. Bailey, Michael Wigler, Susanne Månér, Jonathan Sebat, Nicholas E. Navin, Pär Lundin and B. Lakshmi and has published in prestigious journals such as Science, Journal of Biological Chemistry and Blood.

In The Last Decade

Hillary F. Massa

27 papers receiving 3.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Large-Scale Copy Number Polymorphism in the Human Genome

2004 1.8k citations Janet M. Young, Hillary F. Massa et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hillary F. Massa United States	20	2.2k	2.1k	1.1k	461	348	27	3.9k
Tom Strachan United Kingdom	36	1.7k 0.8×	4.2k 2.0×	535 0.5×	219 0.5×	296 0.9×	69	5.7k
Delphine Samson France	11	1.4k 0.6×	2.0k 0.9×	505 0.5×	211 0.5×	227 0.7×	13	4.1k
Eric Seboun United States	12	1.3k 0.6×	1.8k 0.8×	298 0.3×	202 0.4×	853 2.5×	24	3.9k
Rudolf Jaenisch United States	22	2.0k 0.9×	3.9k 1.8×	237 0.2×	394 0.9×	719 2.1×	27	5.8k
Sabine Fauré France	7	1.1k 0.5×	1.9k 0.9×	272 0.2×	173 0.4×	195 0.6×	10	3.3k
Stanley M. Gartler United States	42	3.3k 1.5×	4.7k 2.2×	751 0.7×	435 0.9×	264 0.8×	133	6.8k
Donna Karolchik United States	17	1.3k 0.6×	4.3k 2.0×	693 0.6×	945 2.0×	269 0.8×	21	5.3k
Richard J. Gibbons United Kingdom	42	2.5k 1.1×	5.3k 2.5×	459 0.4×	530 1.1×	321 0.9×	104	6.9k
Pouya Kheradpour United States	14	703 0.3×	3.1k 1.5×	435 0.4×	621 1.3×	217 0.6×	17	3.8k
Aaron M. Wenger United States	21	1.7k 0.8×	4.2k 2.0×	488 0.4×	818 1.8×	458 1.3×	33	5.7k

Countries citing papers authored by Hillary F. Massa

Since Specialization

Citations

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

Fields of papers citing papers by Hillary F. Massa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hillary F. Massa. 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 Hillary F. Massa. The network helps show where Hillary F. Massa may publish in the future.

Co-authorship network of co-authors of Hillary F. Massa

This figure shows the co-authorship network connecting the top 25 collaborators of Hillary F. Massa. A scholar is included among the top collaborators of Hillary F. Massa 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 Hillary F. Massa. Hillary F. Massa 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

Young, Janet M., Hillary F. Massa, Li Hsu, & Barbara J. Trask. (2009). Extreme variability among mammalian V1R gene families. Genome Research. 20(1). 10–18. 110 indexed citations

Loo, Lenora W. M., Douglas I. Grove, Eleanor Williams, et al.. (2004). Array Comparative Genomic Hybridization Analysis of Genomic Alterations in Breast Cancer Subtypes. Cancer Research. 64(23). 8541–8549. 173 indexed citations

Bailey, Jeffrey A., et al.. (2001). Segmental Duplications: Organization and Impact Within the Current Human Genome Project Assembly. Genome Research. 11(6). 1005–1017. 491 indexed citations

Vissinga, Christine, Tiong Chia Yeo, J. Frederick Woessner, et al.. (1999). Identification, characterization, and mapping of a mouse homolog of the gene mutated in Nijmegen breakage syndrome. Cytogenetic and Genome Research. 87(1-2). 80–84. 8 indexed citations

DeSilva, Udaya, Hillary F. Massa, Barbara J. Trask, & Eric D. Green. (1999). Comparative Mapping of the Region of Human Chromosome 7 Deleted in Williams Syndrome. Genome Research. 9(5). 428–436. 53 indexed citations

Rouquier, Sylvie, Hillary F. Massa, Pieter J. de Jong, et al.. (1999). A Genomic Region Encompassing a Cluster of Olfactory Receptor Genes and a Myosin Light Chain Kinase (MYLK) Gene Is Duplicated on Human Chromosome Regions 3q13–q21 and 3p13. Genomics. 56(1). 98–110. 48 indexed citations

Meng, Xiangying, Xiaojun Lu, Zhizhong Li, et al.. (1998). Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes. Human Genetics. 103(5). 590–599. 88 indexed citations

Sharma, Vikram, Parvoneh Poorkaj, Fuki M. Hisama, et al.. (1998). An Expression Map from Human Chromosome 14q24.3. Genomics. 47(2). 314–318. 5 indexed citations

Trask, Barbara J., Cynthia Friedman, Antonia Martín-Gallardo, et al.. (1998). Members of the olfactory receptor gene family are contained in large blocks of DNA duplicated polymorphically near the ends of human chromosomes. Human Molecular Genetics. 7(1). 13–26. 167 indexed citations

10.

Iwabuchi, Kuniyoshi, Bin Li, Hillary F. Massa, et al.. (1998). Stimulation of p53-mediated Transcriptional Activation by the p53-binding Proteins, 53BP1 and 53BP2. Journal of Biological Chemistry. 273(40). 26061–26068. 168 indexed citations

11.

Bartuski, Allison J., Yoshiro Kamachi, Charles Schick, et al.. (1998). A Murine Ortholog of the Human Serpin SCCA2 Maps to Chromosome 1 and Inhibits Chymotrypsin-like Serine Proteinases. Genomics. 54(2). 297–306. 11 indexed citations

12.

Wise, Carol A., Gregory A. Clines, Hillary F. Massa, Barbara J. Trask, & Michael Lovett. (1997). Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family.. Genome Research. 7(1). 10–16. 125 indexed citations

13.

Gorski, Jerome L., et al.. (1996). Cosmids Map Two Incontinentia Pigmenti Type 1 (IP1) Translocation Breakpoints to a 180-kb Region within a 1.2-Mb YAC Contig. Genomics. 35(2). 338–345. 1 indexed citations

14.

Ma, Chi, Barbara J. Trask, Hillary F. Massa, et al.. (1996). LAF4 maps to mouse Chromosome 1 and human Chromosome 2q11.2-q12. Mammalian Genome. 7(6). 467–468. 8 indexed citations

15.

Trask, B. J., Heather C. Mefford, Ger van den Engh, et al.. (1996). Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patients. Human Genetics. 98(6). 710–718. 43 indexed citations

16.

Wilson, Angus C., Julia Parrish, Hillary F. Massa, et al.. (1995). The gene encoding the VP16-accessory protein HCF (HCFC1) resides in human Xq28 and is highly expressed in fetal tissues and the adult kidney. Genomics. 25(2). 462–468. 40 indexed citations

17.

Hudgins, Louanne, Hillary F. Massa, & Christine M. Distèche. (1994). Identification of a microdeletion at 7q21.3 with fluorescence in situ hybridization in a patient with split hand/split foot (ectrodactyly). The American Journal of Human Genetics. 55. 1 indexed citations

18.

Green, Eric D., Valerie V. Braden, Robert S. Fulton, et al.. (1994). Integration of physical, genetic and cytogenetic maps of human chromosome 7: isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers. Human Molecular Genetics. 3(3). 489–501. 47 indexed citations

19.

Trask, Barbara J., Sally Lyman Allen, Hillary F. Massa, et al.. (1993). Studies of Metaphase and Interphase Chromosomes Using Fluorescence In Situ Hybridization. Cold Spring Harbor Symposia on Quantitative Biology. 58(0). 767–775. 69 indexed citations

20.

Trask, Barbara J., Hillary F. Massa, & Margit Burmeister. (1992). Fluorescence in situ hybridization establishes the order cen-DXS28(C7)-DXS67(B24)-DXS68(L1)-tel in human chromosome Xp21.3. Genomics. 13(2). 455–457. 9 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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