Anne Hing

5.6k citations

56 papers · 2.7k indexed · 1 hit paper · h-index 26

Impact in

Developmental Biology top 2%
Genetics top 1%
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Genomic variations and chromosomal abnormalities
- Congenital Ear and Nasal Anomalies

Papers in ⓘ

Developmental Biology 4
Genetics 44
- Craniofacial Disorders and Treatments 35
- Cleft Lip and Palate Research 25
- Genomic variations and chromosomal abnormalities 8
- Ocular Disorders and Treatments 5
- Congenital Ear and Nasal Anomalies 5
- Connective tissue disorders research 4

Co-authors: Michael L. Cunningham (23 shared papers)Carrie L. Heike (13 shared papers)Daniela V. Luquetti (7 shared papers)Timothy C. Cox (4 shared papers)Richard A. Hopper (5 shared papers)Helen Donis-Keller (4 shared papers)Cynthia Helms (3 shared papers)Kelly N. Evans (4 shared papers)
Journals: The Cleft Palate-Craniofacial Journal (5 papers)Birth Defects Research Part A Clinical and Molecular Teratology (3 papers)Genetics in Medicine (3 papers)The American Journal of Human Genetics (3 papers)Journal of Craniofacial Surgery (2 papers)
Partner nations: United States Australia Netherlands

In The Last Decade

Anne Hing

54 papers receiving 2.6k citations

Hit Papers

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Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly 1996 · 501 citations

Peers

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-authors

The 25 scholars most cited alongside Anne Hing, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Anne Hing Line = papers co-authored together Anne Hing links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 56 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly Nature Genetics ·Elena Belloni, Maximilian Muenke, Erich Roessler, G. Traverse, J. Siegel‐Bartelt, Ayala Frumkin, Heather F. Mitchell, Helen Donis-Keller, Cynthia Helms, Anne Hing, Henry H. Heng, Ben F. Koop, Duane W. Martindale, Johanna M. Rommens, L.-C. Tsui, Stephen W. Scherer Hit paper breakdown →	1996	501
2	Microtia: Epidemiology and genetics American Journal of Medical Genetics Part A ·Daniela V. Luquetti, Carrie L. Heike, Anne Hing, Michael L. Cunningham, Timothy C. Cox	2011	305
3	Robin Sequence: From Diagnosis to Development of an Effective Management Plan PEDIATRICS ·Kelly N. Evans, Kathleen C.Y. Sie, Richard A. Hopper, Robin P. Glass, Anne Hing, Michael L. Cunningham	2011	200
4	GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart disease American Journal of Medical Genetics ·Tugce Pehlivan, Barbara R. Pober, Martina Brueckner, Stacey Garrett, Rachel Slaugh, Richard Van Rheeden, David B. Wilson, Michael S. Watson, Anne Hing	1999	142
5	Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity Genetics in Medicine ·Ruxandra Bachmann‐Gagescu, Heather C. Mefford, Charles A. Cowan, Gwen M. Glew, Anne Hing, Stephanie E Wallace, Patricia I. Bader, Aline I. Hamati, Pamela J. Reitnauer, Rosemarie Smith, David W. Stockton, Hiltrud Muhle, Ingo Helbig, Evan E. Eichler, Blake C. Ballif, Jill A. Rosenfeld, Karen D. Tsuchiya	2010	137
6	Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations American Journal of Medical Genetics Part A ·Marianne L. Seto, Anne Hing, Jocelyn Chang, Ming Hu, Kathleen A. Kapp‐Simon, Pravin K. Patel, Barbara K. Burton, Alex A. Kane, Matthew D. Smyth, Richard A. Hopper, Richard G. Ellenbogen, Kevin L. Stevenson, Matthew L. Speltz, Michael L. Cunningham	2007	82
7	Picture Perfect? Reliability of Craniofacial Anthropometry Using Three-Dimensional Digital Stereophotogrammetry Plastic & Reconstructive Surgery ·Carrie L. Heike, Michael L. Cunningham, Anne Hing, Erik Stuhaug, Jacqueline R. Starr	2009	77
8	New Scaphocephaly Severity Indices of Sagittal Craniosynostosis: A Comparative Study with Cranial Index Quantifications The Cleft Palate-Craniofacial Journal ·Salvador Ruíz-Correa, Raymond W. Sze, Jacqueline R. Starr, Hen-Tzu J. Lin, Matthew L. Speltz, Michael L. Cunningham, Anne Hing	2006	70
9	Making the Diagnosis Journal of Craniofacial Surgery ·Craig B. Birgfeld, Babette S. Saltzman, Anne Hing, Carrie L. Heike, Paritosh C. Khanna, Joseph S. Gruss, Richard A. Hopper	2013	69
10	A Human Homeotic Transformation Resulting from Mutations in PLCB4 and GNAI3 Causes Auriculocondylar Syndrome The American Journal of Human Genetics ·Mark J. Rieder, Glenn E. Green, Sarah S. Park, Brendan D. Stamper, Christopher T. Gordon, Jason M. Johnson, Christopher Cunniff, Joshua D. Smith, Sarah B. Emery, Stanislas Lyonnet, Jeanne Amiel, Muriel Holder, Andrew A. Heggie, Michael J. Bamshad, Deborah A. Nickerson, Timothy C. Cox, Anne Hing, Jeremy A. Horst, Michael L. Cunningham	2012	67
11	The morphogenesis of wormian bones: A study of craniosynostosis and purposeful cranial deformation American Journal of Medical Genetics Part A ·Pedro A. Sanchez‐Lara, John M. Graham, Anne Hing, John Lee, Michael L. Cunningham	2007	66
12	Two chromosome 7 dinucleotide repeat polymorphisms at gene loci epidermal growth factor receptor (EGFR) and proα2 (1) collagen (COL1A2) Human Molecular Genetics ·David Chi, Anne Hing, Cindy Helms, T. Steinbrueck, Santosh K. Mishra, Helen Donis-Keller	1992	61
13	A Physical and Transcriptional Map of the Preaxial Polydactyly Locus on Chromosome 7q36 Genomics ·Henk Heus, Anne Hing, Marijke J. van Baren, Marijke Joosse, Guido J. Breedveld, Jen C. Wang, Andrea K. Burgess, Helen Donnis-Keller, Cathleen Berglund, Julia Zguricas, Stephen W. Scherer, Johanna M. Rommens, Ben A. Oostra, Peter Heutink	1999	60
14	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 ·Heather C Mefford, Neil Shafer, Francesca Antonacci, Jesse Tsai, Sarah S. Park, Anne Hing, Mark J. Rieder, Matthew D. Smyth, Matthew L. Speltz, Evan E. Eichler, Michael L. Cunningham	2010	59
15	Chromosome abnormalities in congenital heart disease American Journal of Medical Genetics ·Mark C. Johnson, Anne Hing, Mary K. Wood, Michael S. Watson	1997	58
16	“Mandibulofacial dysostosis with microcephaly” caused by EFTUD2 mutations: Expanding the phenotype American Journal of Medical Genetics Part A ·Daniela V. Luquetti, Anne Hing, Mark J. Rieder, Deborah A. Nickerson, Emily H. Turner, Joshua D. Smith, Sarah Park, Michael L. Cunningham	2012	55
17	Fetus in fetu:Molecular analysis of a fetiform mass American Journal of Medical Genetics ·Anne Hing, Jane E. Corteville, Robert P. Foglia, David P. Bliss, Helen Donis‐Keller, S. Bruce Dowton	1993	42
18	Clinical care in craniofacial microsomia: A review of current management recommendations and opportunities to advance research American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Carrie L. Heike, Anne Hing, Clare Aspinall, S.P. Bartlett, Craig B. Birgfeld, Amelia F. Drake, Luiz André Freire Pimenta, Kathleen C.Y. Sie, Mark M. Urata, Daniela Vivaldi, Daniela V. Luquetti	2013	41
19	Exome Sequencing Identifies a Recurrent De Novo ZSWIM6 Mutation Associated with Acromelic Frontonasal Dysostosis The American Journal of Human Genetics ·Joshua D. Smith, Anne Hing, Christine M. Clarke, Nathan M. Johnson, Francisco A. Perez, Sarah S. Park, Jeremy A. Horst, Brig Mecham, Lisa Maves, Deborah A. Nickerson, Michael L. Cunningham	2014	40
20	Cleidocranial dysplasia with severe parietal bone dysplasia: C‐terminalRUNX2mutations Birth Defects Research Part A Clinical and Molecular Teratology ·Michael L. Cunningham, Marianne L. Seto, Anne Hing, Marilyn J. Bull, Robert J. Hopkin, Kathleen A. Leppig	2006	36

About Anne Hing

Anne Hing is a scholar working on Developmental Biology, Genetics, Genetics, Molecular Biology and Oral Surgery, having authored 56 papers that have together received 2.7k indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (35 papers), Cleft Lip and Palate Research (25 papers), Genomic variations and chromosomal abnormalities (8 papers), dental development and anomalies (7 papers), Congenital heart defects research (6 papers), Ocular Disorders and Treatments (5 papers), Congenital Ear and Nasal Anomalies (5 papers) and Connective tissue disorders research (4 papers). The work is most often cited by research in Developmental Biology (152 citations), Genetics (1.6k citations), Otorhinolaryngology (153 citations), Genetics (261 citations) and Molecular Biology (1.3k citations). Anne Hing has collaborated with scholars based in United States, Australia and Netherlands. Frequent 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. Their work appears in journals such as The Cleft Palate-Craniofacial Journal, Birth Defects Research Part A Clinical and Molecular Teratology, Genetics in Medicine, The American Journal of Human Genetics and Journal of Craniofacial Surgery.

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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