Kwame Anyane‐Yeboa

5.6k citations

66 papers · 2.3k indexed · h-index 26

Molecular Biology top 10%
Genetics top 1%
Pediatrics, Perinatology and Child Health top 5%
Surgery
Epidemiology top 10%

Co-authors: Dorothy Warburton Stephen Brown Ashley Wilson Wendy K. Chung Steven L. Gersen Edwin R. Guzman Vaidehi Jobanputra Christina Sobin
Topics: Genomic variations and chromosomal abnormalities (18 papers)Prenatal Screening and Diagnostics (11 papers)Genomics and Rare Diseases (7 papers)
Cited by: Genetics Developmental Biology Molecular Biology
Journals: Nature Genetics The Journal of Clinical Endocrinology & Metabolism American Journal of Public Health
Partner nations: United States Canada Netherlands

In The Last Decade

Kwame Anyane‐Yeboa

66 papers receiving 2.2k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Assessment of the beliefs, needs, and expectations for genetic counseling of patients with hypermobile Ehlers‐Danlos syndrome 2022 ·American Journal of Medical Genetics Part A ·Priyanka Ahimaz,(unknown),(unknown),(unknown),Rebecca Hernan,Kwame Anyane‐Yeboa,Elaine M. Pereira	4
2	Clinical Real-Time Genome Sequencing to Solve the Complex and Confounded Presentation of a Child With Focal Segmental Glomerulosclerosis and Multiple Malignancies 2022 ·Kidney International Reports ·Namrata G. Jain,Dina Ahram,Maddalena Marasà,Ateeq Ur Rehman,(unknown),Stergios Zacharoulis,Anya Revah‐Politi,(unknown),(unknown),Vimla S. Aggarwal,Gunnar Hargus,Kwame Anyane‐Yeboa,Vivette D. D’Agati,Fangming Lin,Vaidehi Jobanputra,Simone Sanna‐Cherchi	2
3	New Insights into the Genetics of Fetal Megacystis: ACTG2 Mutations, Encoding γ-2 Smooth Muscle Actin in Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (Berdon Syndrome) 2015 ·Fetal Diagnosis and Therapy ·(unknown),Sha Tang,Russell S. Miller,Luis Rohena,Layla Shahmirzadi,Kelly Gonzalez,Xiang Li,Charles A. LeDuc,Jiancheng Guo,Ashley Wilson,(unknown),Kenneth I. Glassberg,Heidi Rotterdam,Antonia R. Sepulveda,Wenqi Zeng,Wendy K. Chung,Kwame Anyane‐Yeboa	40
4	FTO variant associated with malformation syndrome 2015 ·American Journal of Medical Genetics Part A ·Luis Rohena,(unknown),Edwin R. Guzman,Mythily Ganapathi,Megan T. Cho,Eden Haverfield,Kwame Anyane‐Yeboa	14
5	Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome: Case Report and Review of Prenatal Ultrasonographic Findings 2014 ·Fetal Diagnosis and Therapy ·(unknown),Kwame Anyane‐Yeboa,(unknown),Kenneth I. Glassberg,Russell S. Miller	27
6	Rare inheritance of Leri-Weill Syndrome due to crossover of short stature Homeobox Gene (SHOX) Deletions between X and Y Chromosomes: a case report 2013 ·International Journal of Pediatric Endocrinology ·Marisa Censani,Kwame Anyane‐Yeboa,Ronald J. Wapner,Erica Spiegel,Edwin R. Guzman,Sharon E. Oberfield	2
7	The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease 2013 ·Human Genetics ·Dorothy Warburton,Michael Ronemus,Jennie Kline,Vaidehi Jobanputra,Ismee Williams,Kwame Anyane‐Yeboa,Wendy K. Chung,Lan Yu,Nancy Wong,Danielle Awad,Chih‐Yu Yu,Anthony Leotta,Jude Kendall,Boris Yamrom,Yoon-ha Lee,Michael Wigler,Dan Levy	80
8	CM-AVM syndrome in a neonate: case report and treatment with a novel flow reduction strategy 2012 ·PubMed ·Gerald Behr,Leonardo Liberman,Jocelyn Compton,Maria C. Garzón,Kimberly D. Morel,Christine T. Lauren,Thomas J. Starc,(unknown),(unknown),(unknown),Kwame Anyane‐Yeboa,Philip M. Meyers,Emile Bacha,Jessica J. Kandel	10
9	Retinoblastoma Presenting in a Child with Hypomelanosis of Ito 2011 ·The Open Ophthalmology Journal ·Tarek El-Sawy,(unknown),Michael F. Chiang,Kwame Anyane‐Yeboa,Kimberly D. Morel,Robert Folberg,Brian P. Marr,David M. Abramson	4
10	Duplication of the ZIC2 gene is not associated with holoprosencephaly 2011 ·American Journal of Medical Genetics Part A ·Vaidehi Jobanputra,(unknown),Kwame Anyane‐Yeboa,Anita Shanmugham,(unknown),Stephen Brown,Peter E. Warburton,Brynn Levy,Dorothy Warburton	21
11	Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH 2010 ·American Journal of Medical Genetics Part A ·Sibel Kantarci,Kate G. Ackerman,Meaghan Russell,Mauro Longoni,Carrie Sougnez,Kristin Noonan,Eli Hatchwell,Xiaoyun Zhang,(unknown),Kwame Anyane‐Yeboa,Paul W. Dickman,Jay M. Wilson,Patricia K. Donahoe,Barbara R. Pober	40
12	A Novel Mutation Causing Pseudohypoparathyroidism 1A with Congenital Hypothyroidism and Osteoma Cutis 2009 ·Journal of Clinical Research in Pediatric Endocrinology ·(unknown),Maria C. Garzón,Kwame Anyane‐Yeboa,Bina Shah	9
13	Changes in an inherited ring (22) due to meiotic recombination? Implications for genetic counseling 2009 ·American Journal of Medical Genetics Part A ·Vaidehi Jobanputra,(unknown),Kwame Anyane‐Yeboa,Dorothy Warburton,Brynn Levy	20
14	Application of ROMA (representational oligonucleotide microarray analysis) to patients with cytogenetic rearrangements 2005 ·Genetics in Medicine ·Vaidehi Jobanputra,Jonathan Sebat,Jennifer Troge,Wendy K. Chung,Kwame Anyane‐Yeboa,Michael Wigler,Dorothy Warburton	26
15	Networks of Attention in Children With the 22q11 Deletion Syndrome 2004 ·Developmental Neuropsychology ·Christina Sobin,Karen Kiley‐Brabeck,(unknown),Maude L. Blundell,Kwame Anyane‐Yeboa,Maria Karayiorgou	84
16	Homozygosity for Multiple Contiguous Single-Nucleotide Polymorphisms as an Indicator of Large Heterozygous Deletions: Identification of a Novel Heterozygous 8-kb Intragenic Deletion (IVS7–19 to IVS15–17) in a Patient with Glycogen Storage Disease Type II 2002 ·The American Journal of Human Genetics ·Maryann L. Huie,Kwame Anyane‐Yeboa,Edwin R. Guzman,Rochelle Hirschhorn	25
17	Cerebro-Oculo-Facio-Skeletal Syndrome with a Nucleotide Excision–Repair Defect and a Mutated XPD Gene, with Prenatal Diagnosis in a Triplet Pregnancy 2001 ·The American Journal of Human Genetics ·John M. Graham,Kwame Anyane‐Yeboa,Anja Raams,Esther Appeldoorn,Wim J. Kleijer,Victor H. Garritsen,David B. Busch,(unknown),Nicolaas G.J. Jaspers	85
18	Lumbar gibbus in storage diseases and bone dysplasias 1997 ·Pediatric Radiology ·(unknown),W. E. Berdon,Ralph S. Lachman,Kwame Anyane‐Yeboa,Carrie Ruzal‐Shapiro,David P. Roye	29
19	Caveat to genotype-phenotype correlation in mucopolysaccharidosis type II: Discordant clinical severity of R468W and R468Q mutations of the iduronate-2-sulfatase gene 1993 ·Human Mutation ·Chester B. Whitley,(unknown),Elena L. Aronovich,Paul Crotty,Kwame Anyane‐Yeboa,Donna Russo,(unknown)	32
20	Myelomeningocele, Arnold‐Chiari anomaly and hydrocephalus in focal dermal hypoplasia 1988 ·American Journal of Medical Genetics ·(unknown),Kwame Anyane‐Yeboa,Marc E. Grossman,Ted Rosén	14

About Kwame Anyane‐Yeboa

Kwame Anyane‐Yeboa is a scholar working on Genetics, Genetics and Urology, having authored 66 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (11 papers) and Genomics and Rare Diseases (7 papers). The work is most often cited by research in Genetics (1.2k citations), Developmental Biology (45 citations) and Molecular Biology (1.3k citations). Kwame Anyane‐Yeboa has collaborated with scholars based in United States, Canada and Netherlands. Frequent 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 Maude L. Blundell. Their work appears in journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and American Journal of Public Health.

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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