F.F.B. Elder

5.2k citations

76 papers · 3.9k indexed · h-index 31

Impact in

Genetics top 0.5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Genetic diversity and population structure
- Genetics and Neurodevelopmental Disorders
Molecular Biology top 5%
- Congenital heart defects research
- Sexual Differentiation and Disorders

Papers in ⓘ

Genetics 46
- Genomic variations and chromosomal abnormalities 13
- Genetic diversity and population structure 12
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 12
- Genetic Mapping and Diversity in Plants and Animals 7
Paleontology 7
- Evolution and Paleontology Studies 7

Co-authors: Wilbur R. Harrison (15 shared papers)Terence J. Robinson (15 shared papers)Andrew R. Zinn (11 shared papers)Paul A. Overbeek (5 shared papers)Judith L. Ross (8 shared papers)Frank Greenberg (5 shared papers)Takahiko Yokoyama (1 shared paper)Nancy A. Jenkins (1 shared paper)
Journals: Cytogenetic and Genome Research (13 papers)Genomics (4 papers)Prenatal Diagnosis (3 papers)Mammalian Genome (3 papers)Nature Genetics (3 papers)
Partner nations: United States South Africa United Kingdom

In The Last Decade

F.F.B. Elder

75 papers receiving 3.7k citations

Peers

Countries citing papers authored by F.F.B. Elder

Since Specialization

Citations

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

Fields of papers citing papers by F.F.B. Elder

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside F.F.B. Elder, 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 F.F.B. Elder Line = papers co-authored together F.F.B. Elder 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 76 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Reversal of Left-Right Asymmetry: a Situs Inversus Mutation Science ·Takahiko Yokoyama, Neal G. Copeland, Nancy A. Jenkins, Charles A. Montgomery, F.F.B. Elder, Paul A. Overbeek	1993	361
2	Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia Nature Genetics ·Jacqueline T. Hecht, Laura D. Nelson, Eric Crowder, Yang Wang, F.F.B. Elder, Wilbur R. Harrison, Clair A. Francomano, Christa Prange, Gregory G. Lennon, Michelle Deere, Jack Lawler	1995	304
3	Yeast stimulation of bone marrow mitosis for cytogenetic investigations Cytogenetic and Genome Research ·M.R. Lee, F.F.B. Elder	1980	257
4	Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis Nature Genetics ·Melanie M. Sohocki, Sara J. Bowne, Lori S. Sullivan, Seth Blackshaw, Constance L. Cepko, Annette Payne, Shomi Bhattacharya, Shagufta Khaliq, S. Qasim Mehdi, David G. Birch, Wilbur R. Harrison, F.F.B. Elder, John R. Heckenlively, Stephen P. Daiger	2000	229
5	Chromosome 1p36 Deletions: The Clinical Phenotype and Molecular Characterization of a Common Newly Delineated Syndrome The American Journal of Human Genetics ·Stuart K. Shapira, Christopher McCaskill, Hope Northrup, Aimee S. Spikes, F.F.B. Elder, V. Reid Sutton, Julie R. Korenberg, Frank Greenberg, Lisa G. Shaffer	1997	201
6	Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse Nature Genetics ·David O. Morgan, Lee Turnpenny, Judith Goodship, Weilie Dai, Kumud Majumder, Lucy Matthews, Alison Gardner, Gaby Schuster, Long Vien, Wilbur R. Harrison, F.F.B. Elder, Miranda Penman-Splitt, Paul A. Overbeek, Tom Strachan	1998	190
7	Cytogenetic findings in a prospective series of patients with DiGeorge anomaly. PubMed ·Frank Greenberg, F.F.B. Elder, Paula Haffner, Hope Northrup, David H. Ledbetter	1988	138
8	Phenotypes Associated with SHOX Deficiency The Journal of Clinical Endocrinology & Metabolism ·Judith L. Ross, Charles I. Scott, Pia Marttila, Karen Kowal, Andrea Naß, Peter Papenhausen, Jack Abboudi, Lee Osterman, Harvey Kushner, Paul Carter, Marybeth Ezaki, F.F.B. Elder, Fanglin Wei, Huaqun Chen, Andrew R. Zinn	2001	136
9	Cognitive and motor development during childhood in boys with Klinefelter syndrome American Journal of Medical Genetics Part A ·Judith L. Ross, David P. Roeltgen, Gerry A. Stefanatos, Rebecca Benecke, Martha P.D. Zeger, Harvey Kushner, Purita Ramos, F.F.B. Elder, Andrew R. Zinn	2008	135
10	Early Androgen Deficiency in Infants and Young Boys with 47,XXY Klinefelter Syndrome Hormone Research in Paediatrics ·Judith L. Ross, Carole Samango‐Sprouse, Najiba Lahlou, Karen Kowal, F.F.B. Elder, Andrew R. Zinn	2005	117
11	Androgen Receptor CAG_nRepeat Length Influences Phenotype of 47,XXY (Klinefelter) Syndrome The Journal of Clinical Endocrinology & Metabolism ·Andrew R. Zinn, Purita Ramos, F.F.B. Elder, Karen Kowal, Carole Samango‐Sprouse, Judith L. Ross	2005	91
12	Paracentric inversions in humans: A review of 446 paracentric inversions with presentation of 120 new cases American Journal of Medical Genetics ·Mark J. Pettenati, P. Nagesh Rao, Mary C. Phelan, Frank S. Grass, Kathleen W. Rao, Paula C. Cosper, A J Carroll, F.F.B. Elder, Jennifer L. Smith, Michael D. Higgins, J. T. Lanman, Rodney R. Higgins, Merlin G. Butler, Frederick W. Luthardt, E. Keitges, Colleen Jackson‐Cook, J.A. Brown, Stephanie P. Schwartz, D L Van Dyke, C. G. Palmer	1995	82
13	Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4. PubMed ·Michael R. Altherr, Ulla Bengtsson, F.F.B. Elder, David H. Ledbetter, John J. Wasmuth, Megan McDonald, James F. Gusella, Frank Greenberg	1991	81
14	Complete SHOX deficiency causes Langer mesomelic dysplasia American Journal of Medical Genetics ·Andrew R. Zinn, Fanglin Wei, Ling Zhang, F.F.B. Elder, Charles I. Scott, Pia Marttila, Judith L. Ross	2002	80
15	Characterization of telomerase-immortalized, non-neoplastic, human Barrett’s cell line (BAR-T) Diseases of the Esophagus ·Kshama Jaiswal, Carmela P. Morales, Linda A. Feagins, Kenia Gandia, X. Zhang, H.-Y. Zhang, Kadija‐Kathy Hormi‐Carver, Yuenan Shen, F.F.B. Elder, Ruben D. Ramirez, George A. Sarosi, Stuart J. Spechler, Rhonda F. Souza	2007	76
16	Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease Pediatric Research ·Ashleigh A. Richards, Lane J. Jaeckle Santos, Haley A. Nichols, Bill P. Crider, F.F.B. Elder, Natalie Hauser, Andrew R. Zinn, Vidu Garg	2008	74
17	A molecular cytogenetic analysis of X chromosome repatterning in the Bovidae: transpositions, inversions, and phylogenetic inference Cytogenetic and Genome Research ·Terence J. Robinson, Wilbur R. Harrison, F. Abel Ponce de Léon, Stacy Davis, F.F.B. Elder	1998	57
18	PRENATAL DIAGNOSIS OF UNIPARENTAL DISOMY 15 FOLLOWING TRISOMY 15 MOSAICISM Prenatal Diagnosis ·Susan L. Christian, Ann C. M. Smith, Michelle Macha, Susan H. Black, F.F.B. Elder, JAMIE M.-P. JOHNSON, Robert G. Resta, Urvashi Surti, Lorraine Suslak, Marion S. Verp, David H. Ledbetter	1996	55
19	Insertional Mutation of the Collagen Genes Col4a3 and Col4a4 in a Mouse Model of Alport Syndrome Genomics ·Wei Lü, Carrie L. Phillips, Paul D. Killen, Tommy Hlaing, Wilbur R. Harrison, F.F.B. Elder, Jeffrey H. Miner, Paul A. Overbeek, Miriam H. Meisler	1999	54
20	A Turner syndrome neurocognitive phenotype maps to Xp22.3 Behavioral and Brain Functions ·Andrew R. Zinn, David P. Roeltgen, Gerry A. Stefanatos, Purita Ramos, F.F.B. Elder, Harvey Kushner, Karen Kowal, Judith L. Ross	2007	52

About F.F.B. Elder

F.F.B. Elder is a scholar working on Genetics, Paleontology, Aging, Molecular Biology and Plant Science, having authored 76 papers that have together received 3.9k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (20 papers), Genomic variations and chromosomal abnormalities (13 papers), Genetic diversity and population structure (12 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers), Genetic Mapping and Diversity in Plants and Animals (7 papers), Evolution and Paleontology Studies (7 papers) and Congenital heart defects research (6 papers). The work is most often cited by research in Genetics (2.2k citations), Molecular Biology (2.1k citations), Immunology and Allergy (148 citations), Paleontology (163 citations) and Aging (38 citations). F.F.B. Elder has collaborated with scholars based in United States, South Africa and United Kingdom. Frequent co-authors include Wilbur R. Harrison, Terence J. Robinson, Andrew R. Zinn, Paul A. Overbeek, Judith L. Ross, Frank Greenberg, Takahiko Yokoyama, Nancy A. Jenkins, Charles A. Montgomery and Neal G. Copeland. Their work appears in journals such as Cytogenetic and Genome Research, Genomics, Prenatal Diagnosis, Mammalian Genome and Nature Genetics.

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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