H.F. Willard

6.0k total citations · 1 hit paper
45 papers, 4.1k citations indexed

About

H.F. Willard is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, H.F. Willard has authored 45 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 21 papers in Genetics and 12 papers in Plant Science. Recurrent topics in H.F. Willard's work include Chromosomal and Genetic Variations (12 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers). H.F. Willard is often cited by papers focused on Chromosomal and Genetic Variations (12 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers). H.F. Willard collaborates with scholars based in United States, Canada and United Kingdom. H.F. Willard's co-authors include John A. McNeil, Jeanne B. Lawrence, Christine Clemson, M.H. Skolnick, Rachel Wevrick, John S. Waye, S.A. Latt, L.A. Menlove, Anthony P. Monaco and David H. Ledbetter and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Journal of Cell Biology.

In The Last Decade

H.F. Willard

44 papers receiving 4.0k citations

Hit Papers

XIST RNA paints the inactive X chromosome at interphase: ... 1996 2026 2006 2016 1996 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H.F. Willard United States 28 2.8k 2.1k 966 442 337 45 4.1k
A. Craig Chinault United States 46 4.1k 1.5× 2.8k 1.3× 780 0.8× 741 1.7× 250 0.7× 99 5.8k
Michele D’Urso Italy 35 2.8k 1.0× 1.4k 0.7× 423 0.4× 706 1.6× 221 0.7× 100 4.2k
O. J. Miller United States 33 2.9k 1.1× 1.8k 0.8× 1.5k 1.5× 251 0.6× 227 0.7× 86 4.5k
A. Westerveld Netherlands 44 4.3k 1.5× 1.4k 0.7× 414 0.4× 311 0.7× 876 2.6× 153 6.1k
Heidemarie Neitzel Germany 30 2.5k 0.9× 1.5k 0.7× 605 0.6× 302 0.7× 448 1.3× 95 4.0k
E. Viégas-Pèquignot France 33 4.2k 1.5× 2.0k 1.0× 810 0.8× 587 1.3× 474 1.4× 92 6.0k
Helen J. Eyre Australia 33 2.3k 0.8× 1.5k 0.7× 475 0.5× 253 0.6× 203 0.6× 63 3.8k
Holger Hoehn Germany 37 3.1k 1.1× 1.1k 0.5× 736 0.8× 520 1.2× 937 2.8× 135 4.3k
Veronica J. Buckle United Kingdom 47 4.6k 1.6× 2.1k 1.0× 1.3k 1.3× 359 0.8× 476 1.4× 91 6.5k
Park S. Gerald United States 34 1.8k 0.6× 1.2k 0.6× 352 0.4× 484 1.1× 271 0.8× 111 3.6k

Countries citing papers authored by H.F. Willard

Since Specialization
Citations

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

Fields of papers citing papers by H.F. Willard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H.F. Willard

This figure shows the co-authorship network connecting the top 25 collaborators of H.F. Willard. A scholar is included among the top collaborators of H.F. Willard 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 H.F. Willard. H.F. Willard 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.
Clemson, Christine, John A. McNeil, H.F. Willard, & Jeanne B. Lawrence. (1996). XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure.. The Journal of Cell Biology. 132(3). 259–275. 645 indexed citations breakdown →
2.
Naumova, Anna K., Robert M. Plenge, Lynne M. Bird, et al.. (1996). Heritability of X chromosome--inactivation phenotype in a large family.. PubMed. 58(6). 1111–9. 148 indexed citations
3.
Hendrich, Brian & H.F. Willard. (1995). Epigenetic regulation of gene expression: the effect of altered chromatin structure from yeast to mammals. Human Molecular Genetics. 4(suppl_1). 1765–1777. 66 indexed citations
4.
Rack, Katrina, Jamel Chelly, Richard J. Gibbons, et al.. (1994). Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia. Human Molecular Genetics. 3(7). 1053–1059. 61 indexed citations
5.
Willard, H.F., Carolyn J. Brown, Laura Carrel, Brian Hendrich, & Andrew P. Miller. (1993). Epigenetic and Chromosomal Control of Gene Expression: Molecular and Genetic Analysis of X Chromosome Inactivation. Cold Spring Harbor Symposia on Quantitative Biology. 58(0). 315–322. 37 indexed citations
6.
Bascom, R.A., Jaime Garcia‐Heras, C L Hsieh, et al.. (1992). Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM.. Europe PMC (PubMed Central). 51(5). 1028–35. 31 indexed citations
7.
Garcia‐Heras, Jaime, et al.. (1991). Localization of histidase to human chromosome region 12q22→q24.1 and mouse chromosome region 10C2→D1. Cytogenetic and Genome Research. 56(3-4). 178–181. 15 indexed citations
8.
Greig, Gillian, Sumit Parikh, Julia B. George, Vicki E. C. Powers, & H.F. Willard. (1991). Molecular cytogenetics of α satellite DNA from chromosome 12: fluorescence in situ hybridization and description of DNA and array length polymorphisms. Cytogenetic and Genome Research. 56(3-4). 144–148. 19 indexed citations
9.
Davies, Kay E., Jean‐Louis Mandel, Anthony P. Monaco, et al.. (1990). Report of the committee on the genetic constitution of the X chromosome (Part 1 of 3). Cytogenetic and Genome Research. 55(1-4). 254–272. 489 indexed citations
10.
Greig, Gillian, et al.. (1989). Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16.. PubMed. 45(6). 862–72. 66 indexed citations
11.
Kidd, K.K., A. Bowcock, J. Schmidtke, et al.. (1989). Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 922–947. Cytogenetic and Genome Research. 51(1-4). 922–947. 1 indexed citations
12.
Kidd, K.K., A. Bowcock, P. Pearson, et al.. (1988). Report of the committee on human gene mapping by recombinant DNA techniques (Part 1 of 6). Cytogenetic and Genome Research. 49(1-3). 132–145. 11 indexed citations
13.
Willard, H.F., et al.. (1987). Genetic linkage analysis of the pericentromeric region of the human x chromosome using polymorphic alpha satellite dna. 46. 716. 14 indexed citations
14.
Willard, H.F., M.H. Skolnick, P. Pearson, & J.-L. Mandel. (1985). Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques (Part 1 of 5). Cytogenetic and Genome Research. 40(1-4). 360–385. 74 indexed citations
15.
Willard, H.F., M.H. Skolnick, P. Pearson, & J.-L. Mandel. (1985). Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques (Part 5 of 5). Cytogenetic and Genome Research. 40(1-4). 465–489. 1 indexed citations
16.
Skolnick, M.H., H.F. Willard, & L.A. Menlove. (1984). Report of the committee on human gene mapping by recombinant DNA techniques. Cytogenetic and Genome Research. 37(1-4). 210–273. 247 indexed citations
17.
Willard, H.F., et al.. (1980). Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblasts.. PubMed. 32(1). 16–25. 21 indexed citations
18.
Mellman, Ira, et al.. (1979). Cobalamin coenzyme synthesis in normal and mutant human fibroblasts. Evidence for a processing enzyme activity deficient in cblC cells.. Journal of Biological Chemistry. 254(23). 11847–11853. 66 indexed citations
19.
Willard, H.F., Ira Mellman, & Leah Rosenberg. (1978). Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 30(1). 1–13. 93 indexed citations
20.
Willard, H.F. & S.A. Latt. (1976). Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy.. PubMed. 28(3). 213–27. 118 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

Rankless by CCL
2026