Kwame Anyane‐Yeboa

5.6k total citations
66 papers, 2.3k citations indexed

About

Kwame Anyane‐Yeboa is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Kwame Anyane‐Yeboa has authored 66 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 32 papers in Molecular Biology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Kwame Anyane‐Yeboa's work include Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (11 papers) and Genomics and Rare Diseases (7 papers). Kwame Anyane‐Yeboa is often cited by papers focused on Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (11 papers) and Genomics and Rare Diseases (7 papers). Kwame Anyane‐Yeboa collaborates with scholars based in United States, Canada and Netherlands. Kwame Anyane‐Yeboa's co-authors include Dorothy Warburton, Dorothy Warburton, Stephen Brown, Ashley Wilson, Wendy K. Chung, Steven L. Gersen, Edwin R. Guzman, Vaidehi Jobanputra, Christina Sobin and Karen Kiley‐Brabeck and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and American Journal of Public Health.

In The Last Decade

Kwame Anyane‐Yeboa

66 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kwame Anyane‐Yeboa United States 26 1.3k 1.2k 361 277 270 66 2.3k
J P Fryns Belgium 25 1.1k 0.9× 1.2k 1.0× 430 1.2× 304 1.1× 176 0.7× 90 2.2k
Sulagna C. Saitta United States 24 1.1k 0.9× 1.0k 0.8× 219 0.6× 180 0.6× 244 0.9× 42 1.9k
Mitsuo Masuno Japan 21 1.4k 1.1× 1.1k 0.9× 180 0.5× 275 1.0× 216 0.8× 86 2.3k
Alan Shanske United States 26 976 0.8× 931 0.7× 310 0.9× 240 0.9× 142 0.5× 84 1.9k
Margherita Silengo Italy 29 2.0k 1.6× 1.7k 1.4× 617 1.7× 489 1.8× 273 1.0× 114 3.3k
Seema R. Lalani United States 30 1.5k 1.2× 1.6k 1.3× 481 1.3× 360 1.3× 293 1.1× 98 2.9k
Koji Muroya Japan 28 1.9k 1.5× 1.9k 1.5× 301 0.8× 377 1.4× 94 0.3× 119 3.1k
Maria Hoeltzenbein Germany 23 899 0.7× 794 0.6× 237 0.7× 272 1.0× 111 0.4× 54 2.8k
Małgorzata Krajewska‐Walasek Poland 23 1.4k 1.1× 1.0k 0.8× 329 0.9× 298 1.1× 129 0.5× 110 2.2k
Dvorah Abeliovich Israel 31 1.5k 1.2× 1.4k 1.1× 450 1.2× 340 1.2× 72 0.3× 98 3.0k

Countries citing papers authored by Kwame Anyane‐Yeboa

Since Specialization
Citations

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

Fields of papers citing papers by Kwame Anyane‐Yeboa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kwame Anyane‐Yeboa. 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 Kwame Anyane‐Yeboa. The network helps show where Kwame Anyane‐Yeboa may publish in the future.

Co-authorship network of co-authors of Kwame Anyane‐Yeboa

This figure shows the co-authorship network connecting the top 25 collaborators of Kwame Anyane‐Yeboa. A scholar is included among the top collaborators of Kwame Anyane‐Yeboa 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 Kwame Anyane‐Yeboa. Kwame Anyane‐Yeboa 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.
Ahimaz, Priyanka, et al.. (2022). Assessment of the beliefs, needs, and expectations for genetic counseling of patients with hypermobile Ehlers‐Danlos syndrome. American Journal of Medical Genetics Part A. 188(11). 3172–3183. 4 indexed citations
2.
Mehkri, Yusuf, et al.. (2022). Presumptive Diagnosis of Pallister-Hall Syndrome Using Magnetic Resonance Imaging. Cureus. 14(1). e21735–e21735. 1 indexed citations
3.
Okur, Volkan, Charles A. LeDuc, Edwin R. Guzman, et al.. (2019). Homozygous noncanonical splice variant in LSM1 in two siblings with multiple congenital anomalies and global developmental delay. Molecular Case Studies. 5(3). a004101–a004101. 4 indexed citations
4.
Rodan, Lance H., Kwame Anyane‐Yeboa, Karen Chong, et al.. (2018). Gain‐of‐function variants in the ODC1 gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities. American Journal of Medical Genetics Part A. 176(12). 2554–2560. 28 indexed citations
5.
Tang, Sha, Russell S. Miller, Luis Rohena, et al.. (2015). New Insights into the Genetics of Fetal Megacystis: ACTG2 Mutations, Encoding γ-2 Smooth Muscle Actin in Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (Berdon Syndrome). Fetal Diagnosis and Therapy. 38(4). 296–306. 40 indexed citations
6.
Rohena, Luis, Edwin R. Guzman, Mythily Ganapathi, et al.. (2015). FTO variant associated with malformation syndrome. American Journal of Medical Genetics Part A. 170(4). 1023–1028. 14 indexed citations
7.
Anyane‐Yeboa, Kwame, et al.. (2014). Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome: Case Report and Review of Prenatal Ultrasonographic Findings. Fetal Diagnosis and Therapy. 36(1). 74–80. 27 indexed citations
8.
Basel‐Vanagaite, Lina, Rüstem Yilmaz, Sha Tang, et al.. (2014). Expanding the clinical and mutational spectrum of Kaufman oculocerebrofacial syndrome with biallelic UBE3B mutations. Human Genetics. 133(7). 939–949. 28 indexed citations
9.
Rita, Debra, et al.. (2012). Molecular diagnostic dilemmas in Rett syndrome. Brain and Development. 34(9). 750–755. 3 indexed citations
10.
Garzón, Maria C., et al.. (2009). A Novel Mutation Causing Pseudohypoparathyroidism 1A with Congenital Hypothyroidism and Osteoma Cutis. Journal of Clinical Research in Pediatric Endocrinology. 1(5). 244–247. 9 indexed citations
11.
Jobanputra, Vaidehi, et al.. (2009). Changes in an inherited ring (22) due to meiotic recombination? Implications for genetic counseling. American Journal of Medical Genetics Part A. 149A(6). 1310–1314. 20 indexed citations
12.
Jobanputra, Vaidehi, Jonathan Sebat, Jennifer Troge, et al.. (2005). Application of ROMA (representational oligonucleotide microarray analysis) to patients with cytogenetic rearrangements. Genetics in Medicine. 7(2). 111–118. 26 indexed citations
13.
Sobin, Christina, et al.. (2004). Networks of Attention in Children With the 22q11 Deletion Syndrome. Developmental Neuropsychology. 26(2). 611–626. 84 indexed citations
14.
Levy, Joseph, Wendy Chung, Maria C. Garzón, et al.. (2002). Congenital myopathy, recurrent secretory diarrhea, bullous eruption of skin, microcephaly, and deafness: A new genetic syndrome?. American Journal of Medical Genetics Part A. 116A(1). 20–25. 2 indexed citations
15.
16.
Graham, John M., Kwame Anyane‐Yeboa, Anja Raams, et al.. (2001). Cerebro-Oculo-Facio-Skeletal Syndrome with a Nucleotide Excision–Repair Defect and a Mutated XPD Gene, with Prenatal Diagnosis in a Triplet Pregnancy. The American Journal of Human Genetics. 69(2). 291–300. 85 indexed citations
17.
Potocki, Lorraine, Sung Sup Park, Marjorie Withers, et al.. (2000). Molecular mechanism for duplication 17p11.2— the homologous recombination reciprocal of the Smith-Magenis microdeletion. Nature Genetics. 24(1). 84–87. 263 indexed citations
18.
Berdon, W. E., et al.. (1997). Lumbar gibbus in storage diseases and bone dysplasias. Pediatric Radiology. 27(4). 289–294. 29 indexed citations
19.
Anyane‐Yeboa, Kwame, et al.. (1988). Myelomeningocele, Arnold‐Chiari anomaly and hydrocephalus in focal dermal hypoplasia. American Journal of Medical Genetics. 30(4). 917–923. 14 indexed citations
20.
Grover, Ranjeet, Stanton Newman, Doris L. Wethers, Kwame Anyane‐Yeboa, & Kenneth A. Pass. (1986). Newborn screening for hemoglobinopathies: the benefit beyond the target.. American Journal of Public Health. 76(10). 1236–1237. 12 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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