Anne Hing

5.6k total citations · 1 hit paper
56 papers, 2.7k citations indexed

About

Anne Hing is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Anne Hing has authored 56 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Genetics, 24 papers in Molecular Biology and 9 papers in Surgery. Recurrent topics in Anne Hing's work include Craniofacial Disorders and Treatments (35 papers), Cleft Lip and Palate Research (25 papers) and Genomic variations and chromosomal abnormalities (8 papers). Anne Hing is often cited by papers focused on Craniofacial Disorders and Treatments (35 papers), Cleft Lip and Palate Research (25 papers) and Genomic variations and chromosomal abnormalities (8 papers). Anne Hing collaborates with scholars based in United States, France and Australia. Anne Hing's co-authors include Michael L. Cunningham, Carrie L. Heike, Daniela V. Luquetti, Timothy C. Cox, Richard A. Hopper, Helen Donis-Keller, Cynthia Helms, Kelly N. Evans, Kathleen C.Y. Sie and Stephen W. Scherer and has published in prestigious journals such as Nature Genetics, PEDIATRICS and The American Journal of Human Genetics.

In The Last Decade

Anne Hing

54 papers receiving 2.6k 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.

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly

1996 501 citations Cynthia Helms, Anne Hing et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anne Hing United States	26	1.6k	1.3k	614	268	261	56	2.7k
Clarisse Baumann France	26	853 0.5×	969 0.8×	495 0.8×	330 1.2×	432 1.7×	73	2.1k
R M Winter United Kingdom	34	2.0k 1.2×	1.6k 1.3×	619 1.0×	143 0.5×	341 1.3×	105	3.3k
Peter Meinecke Germany	31	1.9k 1.2×	2.5k 1.9×	437 0.7×	251 0.9×	319 1.2×	105	4.0k
David J. David Australia	30	2.2k 1.4×	724 0.6×	1.2k 2.0×	299 1.1×	129 0.5×	109	3.1k
N. Philip France	24	829 0.5×	796 0.6×	371 0.6×	278 1.0×	275 1.1×	82	1.9k
Rika Kosaki Japan	25	846 0.5×	1.3k 1.0×	297 0.5×	236 0.9×	204 0.8×	113	2.3k
Thomy de Ravel Belgium	38	1.9k 1.2×	2.0k 1.6×	382 0.6×	475 1.8×	387 1.5×	112	4.2k
Keiko Wakui Japan	28	1.4k 0.8×	1.3k 1.0×	192 0.3×	153 0.6×	115 0.4×	89	2.3k
Alan Shanske United States	26	931 0.6×	976 0.8×	240 0.4×	141 0.5×	100 0.4×	84	1.9k
Muriel Holder‐Espinasse France	26	1.0k 0.6×	1.1k 0.8×	358 0.6×	291 1.1×	169 0.6×	74	2.0k

Countries citing papers authored by Anne Hing

Since Specialization

Citations

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

Fields of papers citing papers by Anne Hing

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Hing

This figure shows the co-authorship network connecting the top 25 collaborators of Anne Hing. A scholar is included among the top collaborators of Anne Hing 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 Anne Hing. Anne Hing 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

Gallagher, Emily R., et al.. (2024). Genetic Testing in Craniofacial Care: Development of Algorithms for Testing Patients with Orofacial Clefting, Branchial Arch Anomalies, and Craniosynostosis. The Cleft Palate-Craniofacial Journal. 62(10). 1764–1773.

Hing, Anne, et al.. (2023). Isolated frontosphenoidal craniosynostosis: An argument for genetic testing. American Journal of Medical Genetics Part A. 191(10). 2651–2655.

Li, Dong, Alanna Strong, David Cassiman, et al.. (2020). De novo loss-of-function variants in X-linked MED12 are associated with Hardikar syndrome in females. Genetics in Medicine. 23(4). 637–644. 22 indexed citations

Wenger, Tara, John P. Dahl, Elizabeth Bhoj, et al.. (2016). Tracheal cartilaginous sleeves in children with syndromic craniosynostosis. Genetics in Medicine. 19(1). 62–68. 22 indexed citations

Smith, Joshua D., Anne Hing, Christine M. Clarke, et al.. (2014). Exome Sequencing Identifies a Recurrent De Novo ZSWIM6 Mutation Associated with Acromelic Frontonasal Dysostosis. The American Journal of Human Genetics. 95(2). 235–240. 40 indexed citations

Gallagher, Emily R., Anne Hing, & Michael L. Cunningham. (2013). Evaluating fontanels in the newborn skull. Contemporary pediatrics. 30(11). 2 indexed citations

Rieder, Mark J., Glenn E. Green, Sarah S. Park, et al.. (2012). A Human Homeotic Transformation Resulting from Mutations in PLCB4 and GNAI3 Causes Auriculocondylar Syndrome. The American Journal of Human Genetics. 91(2). 397–397. 6 indexed citations

Luquetti, Daniela V., Carrie L. Heike, Anne Hing, Michael L. Cunningham, & Timothy C. Cox. (2011). Microtia: Epidemiology and genetics. American Journal of Medical Genetics Part A. 158A(1). 124–139. 305 indexed citations

Cunningham, Michael L., Jeremy A. Horst, Mark J. Rieder, et al.. (2010). IGF1R variants associated with isolated single suture craniosynostosis. American Journal of Medical Genetics Part A. 155(1). 91–97. 26 indexed citations

10.

Bachmann‐Gagescu, Ruxandra, Heather C. Mefford, Charles A. Cowan, et al.. (2010). Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity. Genetics in Medicine. 12(10). 641–647. 137 indexed citations

11.

Mefford, Heather C, Francesca Antonacci, Jesse Tsai, et al.. (2010). Copy number variation analysis in single‐suture craniosynostosis: Multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis. American Journal of Medical Genetics Part A. 152A(9). 2203–2210. 59 indexed citations

12.

Hing, Anne, Eleanor S. Click, Marianne L. Seto, et al.. (2009). Bilateral lambdoid and sagittal synostosis (BLSS): A unique craniosynostosis syndrome or predictable craniofacial phenotype?. American Journal of Medical Genetics Part A. 149A(5). 1024–1032. 16 indexed citations

13.

Seto, Marianne L., Anne Hing, Ming Hu, et al.. (2007). Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations. American Journal of Medical Genetics Part A. 143A(7). 678–686. 82 indexed citations

14.

Cunningham, Michael L., Marianne L. Seto, Anne Hing, et al.. (2006). Cleidocranial dysplasia with severe parietal bone dysplasia: C‐terminalRUNX2mutations. Birth Defects Research Part A Clinical and Molecular Teratology. 76(2). 78–85. 36 indexed citations

15.

Slavotinek, Anne, et al.. (2005). Craniofacial defects of blastogenesis: Duplication of pituitary with cleft palate and orophgaryngeal tumors. American Journal of Medical Genetics Part A. 135A(1). 13–20. 26 indexed citations

16.

Hing, Anne, et al.. (2004). Familial acromelic frontonasal dysostosis: Autosomal dominant inheritance with reduced penetrance. American Journal of Medical Genetics Part A. 128A(4). 374–382. 11 indexed citations

17.

Heike, Carrie L., Marianne L. Seto, Anne Hing, et al.. (2001). Century of Jackson-Weiss syndrome: Further definition of clinical and radiographic findings in ?lost? descendants of the original kindred. American Journal of Medical Genetics. 100(4). 315–324. 16 indexed citations

18.

Hing, Anne, Marijke J. van Baren, Marijke Joosse, et al.. (1999). A Physical and Transcriptional Map of the Preaxial Polydactyly Locus on Chromosome 7q36. Genomics. 57(3). 342–351. 60 indexed citations

19.

Hing, Anne, Cynthia Helms, Rachel Slaugh, et al.. (1995). Linkage of preaxial polydactyly type 2 to 7q36. American Journal of Medical Genetics. 58(2). 128–135. 35 indexed citations

20.

Hing, Anne & S. Bruce Dowton. (1993). Aase syndrome: Novel radiographic features. American Journal of Medical Genetics. 45(4). 413–415. 4 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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