Adam B. Kanis

998 total citations
13 papers, 745 citations indexed

About

Adam B. Kanis is a scholar working on Genetics, Molecular Biology and Ophthalmology. According to data from OpenAlex, Adam B. Kanis has authored 13 papers receiving a total of 745 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 2 papers in Ophthalmology. Recurrent topics in Adam B. Kanis's work include Congenital heart defects research (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Ocular Disorders and Treatments (2 papers). Adam B. Kanis is often cited by papers focused on Congenital heart defects research (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Ocular Disorders and Treatments (2 papers). Adam B. Kanis collaborates with scholars based in United States, Israel and Australia. Adam B. Kanis's co-authors include Val C. Sheffield, Edwin M. Stone, Darryl Nishimura, Shivanand R. Patil, Wallace L.M. Alward, Charles Searby, Julie M. Gastier, Ruth E. Swiderski, Kazuhide Kawase and David S. Walton and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Adam B. Kanis

13 papers receiving 726 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Adam B. Kanis United States	11	477	255	213	144	74	13	745
Tiina Alitalo Finland	20	604 1.3×	332 1.3×	238 1.1×	207 1.4×	88 1.2×	30	964
Tim Footz Canada	17	446 0.9×	190 0.7×	130 0.6×	69 0.5×	84 1.1×	36	728
William Bromley United States	5	609 1.3×	215 0.8×	218 1.0×	68 0.5×	81 1.1×	6	781
Maria Giuseppina Miano Italy	18	880 1.8×	512 2.0×	218 1.0×	55 0.4×	140 1.9×	38	1.2k
Jacqueline Siegel‐Bartelt Canada	8	820 1.7×	477 1.9×	111 0.5×	95 0.7×	44 0.6×	10	1.1k
J.W. Delleman Netherlands	17	360 0.8×	275 1.1×	196 0.9×	142 1.0×	137 1.9×	45	872
Elena Vallespín Spain	20	711 1.5×	349 1.4×	296 1.4×	74 0.5×	75 1.0×	53	944
Richard A Axton United Kingdom	14	611 1.3×	198 0.8×	176 0.8×	42 0.3×	131 1.8×	23	827
Oscar F. Chacón‐Camacho Mexico	12	348 0.7×	211 0.8×	156 0.7×	60 0.4×	43 0.6×	62	533
Sarah Hull United Kingdom	22	812 1.7×	292 1.1×	413 1.9×	146 1.0×	147 2.0×	44	1.1k

Countries citing papers authored by Adam B. Kanis

Since Specialization

Citations

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

Fields of papers citing papers by Adam B. Kanis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Adam B. Kanis. 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 Adam B. Kanis. The network helps show where Adam B. Kanis may publish in the future.

Co-authorship network of co-authors of Adam B. Kanis

This figure shows the co-authorship network connecting the top 25 collaborators of Adam B. Kanis. A scholar is included among the top collaborators of Adam B. Kanis 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 Adam B. Kanis. Adam B. Kanis is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

Sawyer, Taylor, et al.. (2012). A Case of Wolf-Hirschhorn Syndrome and Hypoplastic Left Heart Syndrome. Pediatric Cardiology. 34(5). 1244–1246. 10 indexed citations

Brookes, James, et al.. (2007). Cochlear implantation in deafness-dystonia-optic neuronopathy (DDON) syndrome. International Journal of Pediatric Otorhinolaryngology. 72(1). 121–126. 32 indexed citations

Nishimura, Darryl, Charles Searby, Wallace L.M. Alward, et al.. (2001). A Spectrum of FOXC1 Mutations Suggests Gene Dosage as a Mechanism for Developmental Defects of the Anterior Chamber of the Eye. The American Journal of Human Genetics. 68(2). 364–372. 172 indexed citations

Parvari, Ruti, et al.. (2001). Clinical and genetic characterization of an autosomal dominant nephropathy. American Journal of Medical Genetics. 99(3). 204–209. 10 indexed citations

Ghiasvand, Noor M., Adam B. Kanis, Cynthia Helms, et al.. (2000). Nonsyndromic congenital retinal nonattachment gene maps to human chromosome band 10q21. American Journal of Medical Genetics. 90(2). 165–168. 6 indexed citations

Kanis, Adam B., Ali A. Al‐Rajhi, Christine Taylor, et al.. (1999). Exclusion of AR-CHED from the chromosome 20 region containing the PPMD and AD-CHED loci. Ophthalmic Genetics. 20(4). 243–249. 12 indexed citations

Nishimura, Darryl, Ruth E. Swiderski, Wallace L.M. Alward, et al.. (1998). The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25. Nature Genetics. 19(2). 140–147. 359 indexed citations

Rijhsinghani, Asha, et al.. (1998). Antenatal sonographic diagnosis of club foot with particular attention to the implications and outcomes of isolated club foot. Ultrasound in Obstetrics and Gynecology. 12(2). 103–106. 34 indexed citations

Parvari, Ruti, Eli Hershkovitz, Adam B. Kanis, et al.. (1998). Homozygosity and Linkage-Disequilibrium Mapping of the Syndrome of Congenital Hypoparathyroidism, Growth and Mental Retardation, and Dysmorphism to a 1-cM Interval on Chromosome 1q42-43. The American Journal of Human Genetics. 63(1). 163–169. 45 indexed citations

10.

Walder, Roxanne Y., Michael R. Garrett, Gretel Beck, et al.. (1998). Short tandem repeat polymorphic markers for the rat genome from marker-selected libraries. Mammalian Genome. 9(12). 1013–1021. 13 indexed citations

11.

Chatterjee, Tapan K., Alex Eapen, Adam B. Kanis, & Rory A. Fisher. (1997). Genomic Organization, 5′-Flanking Region, and Chromosomal Localization of the HumanRGS3Gene. Genomics. 45(2). 429–433. 14 indexed citations

12.

Arbour, Nancy C., Joël Zlotogora, Robert G. Knowlton, et al.. (1997). Homozygosity Mapping of Achromatopsia to Chromosome 2 Using DNA Pooling. Human Molecular Genetics. 6(5). 689–694. 35 indexed citations

13.

Norgard, Michael V., Jerome Yankowitz, William J. Rhead, Adam B. Kanis, & Bryan D. Hall. (1996). PRENATAL ULTRASOUND FINDINGS IN HYDROLETHALUS: CONTINUING DIFFICULTIES IN DIAGNOSIS. Prenatal Diagnosis. 16(2). 173–179. 3 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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