Annemarie Sommer

2.7k total citations
63 papers, 1.6k citations indexed

About

Annemarie Sommer is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Annemarie Sommer has authored 63 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 22 papers in Molecular Biology and 8 papers in Rheumatology. Recurrent topics in Annemarie Sommer's work include Craniofacial Disorders and Treatments (7 papers), Connective tissue disorders research (6 papers) and Cleft Lip and Palate Research (5 papers). Annemarie Sommer is often cited by papers focused on Craniofacial Disorders and Treatments (7 papers), Connective tissue disorders research (6 papers) and Cleft Lip and Palate Research (5 papers). Annemarie Sommer collaborates with scholars based in United States, Canada and Netherlands. Annemarie Sommer's co-authors include George W. Waylonis, John M. Opitz, Mark A. Kliewer, Laird G. Jackson, David Fitzpatrick, Angelo Selicorni, Antonie D. Kline, Alex V. Levin, Ian D. Krantz and Matthew Pastore and has published in prestigious journals such as JAMA, PEDIATRICS and The American Journal of Human Genetics.

In The Last Decade

Annemarie Sommer

63 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Annemarie Sommer United States 20 770 695 207 197 151 63 1.6k
J P Fryns Belgium 25 1.2k 1.6× 1.1k 1.6× 430 2.1× 304 1.5× 259 1.7× 90 2.2k
Michael C. Brodsky United States 28 412 0.5× 541 0.8× 355 1.7× 261 1.3× 80 0.5× 199 3.2k
Jean‐Pierre Fryns Belgium 20 454 0.6× 599 0.9× 375 1.8× 386 2.0× 256 1.7× 68 1.6k
Frank A. Billson Australia 26 267 0.3× 721 1.0× 176 0.9× 127 0.6× 53 0.4× 102 2.2k
Richard D. Bagnall Australia 32 481 0.6× 1.6k 2.2× 113 0.5× 163 0.8× 136 0.9× 79 3.3k
Uppala Radhakrishna United States 25 758 1.0× 1.0k 1.5× 174 0.8× 252 1.3× 134 0.9× 81 2.1k
Robert Śmigiel Poland 19 441 0.6× 545 0.8× 191 0.9× 231 1.2× 149 1.0× 142 1.2k
Massimo Pellegrini Italy 20 347 0.5× 702 1.0× 105 0.5× 180 0.9× 50 0.3× 61 1.6k
E. Kirk Neely United States 30 995 1.3× 818 1.2× 167 0.8× 169 0.9× 77 0.5× 47 2.4k
Haruhide Ito Japan 28 157 0.2× 466 0.7× 155 0.7× 567 2.9× 237 1.6× 128 2.7k

Countries citing papers authored by Annemarie Sommer

Since Specialization
Citations

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

Fields of papers citing papers by Annemarie Sommer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annemarie Sommer

This figure shows the co-authorship network connecting the top 25 collaborators of Annemarie Sommer. A scholar is included among the top collaborators of Annemarie Sommer 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 Annemarie Sommer. Annemarie Sommer 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.
2.
Cottrell, Catherine E., Annemarie Sommer, Gail D. Wenger, et al.. (2009). Atypical X‐chromosome inactivation in an X;1 translocation patient demonstrating Xq28 functional disomy. American Journal of Medical Genetics Part A. 149A(3). 408–414. 9 indexed citations
3.
Kline, Antonie D., Ian D. Krantz, Annemarie Sommer, et al.. (2008). Cornelia de Lange syndrome: Clinical review, diagnostic and scoring systems, and anticipatory guidance Am J Med Genet Part A 143A:1287–1296. American Journal of Medical Genetics Part A. 146A(20). 2713–2713. 2 indexed citations
4.
Sommer, Annemarie. (2007). Photo essay—Geroderma osteodysplastica. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 145C(3). 291–292. 2 indexed citations
5.
Kline, Antonie D., Ian D. Krantz, Annemarie Sommer, et al.. (2007). Cornelia de Lange syndrome: Clinical review, diagnostic and scoring systems, and anticipatory guidance. American Journal of Medical Genetics Part A. 143A(12). 1287–1296. 191 indexed citations
6.
Morris, Colleen A., Carolyn Β. Mervis, Holly H. Hobart, et al.. (2003). GTF2I hemizygosity implicated in mental retardation in Williams syndrome: Genotype–phenotype analysis of five families with deletions in the Williams syndrome region. American Journal of Medical Genetics Part A. 123A(1). 45–59. 125 indexed citations
7.
Sommer, Annemarie & Dennis W. Bartholomew. (2003). Craniofacial‐deafness‐hand syndrome revisited. American Journal of Medical Genetics Part A. 123A(1). 91–94. 14 indexed citations
8.
Schrander‐Stumpel, C. T. R. M., C Höweler, Marilyn C. Jones, et al.. (1995). Spectrum of X‐linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): Clinical review with six additional families. American Journal of Medical Genetics. 57(1). 107–116. 45 indexed citations
9.
Sommer, Annemarie. (1993). Occurrence of the Sandifer complex in the Brachmann‐de Lange syndrome. American Journal of Medical Genetics. 47(7). 1026–1028. 21 indexed citations
10.
Sommer, Annemarie, et al.. (1993). Aicardi syndrome, metastatic angiosarcoma of the leg, and scalp lipoma. American Journal of Medical Genetics. 45(5). 594–596. 14 indexed citations
11.
Sommer, Annemarie, et al.. (1992). Autosomal dominant inheritance of tetramelic monodactyly. American Journal of Medical Genetics. 42(1). 51–54. 2 indexed citations
12.
Groß, Eva, et al.. (1991). Congenital myopathy with oculo‐facial abnormalities (Marden‐Walker syndrome). American Journal of Medical Genetics. 39(4). 377–379. 13 indexed citations
13.
Fritsch, Michael H. & Annemarie Sommer. (1991). Handbook of Congenital and Early Onset Hearing Loss. 2 indexed citations
14.
Waylonis, George W., et al.. (1989). Familial Occurrence of Primary Fibromyalgia. Archives of Physical Medicine and Rehabilitation. 70(1). 61–63. 57 indexed citations
15.
Ardinger, Holly H, James W. Hanson, Mary Jo Harrod, et al.. (1986). Further delineation of Weaver syndrome. The Journal of Pediatrics. 108(2). 228–235. 37 indexed citations
16.
Hsia, Y. Edward, et al.. (1982). Familial digeorge syndrome in 7 children. The American Journal of Human Genetics. 34(6). 80. 4 indexed citations
17.
Icard‐Liepkalns, Christine, et al.. (1982). Properties of cloned human glioblastoma cells. Journal of the Neurological Sciences. 57(2-3). 257–264. 17 indexed citations
18.
Ray, Robin, et al.. (1980). Lower limb anomalies in the thrombocytopenia absent‐radius (TAR) syndrome. American Journal of Medical Genetics. 7(4). 523–528. 11 indexed citations
19.
Greenwood, Ronald D., et al.. (1977). Congenital Heart Disease in de Langeʼs Syndrome. Southern Medical Journal. 70(1). 80–80. 7 indexed citations
20.
Sommer, Annemarie, et al.. (1970). Achondroplasia and Down's syndrome.. Journal of Medical Genetics. 7(1). 63–66. 7 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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