Sallie B. Freeman

3.8k citations

28 papers · 2.5k indexed · h-index 20

Pediatrics, Perinatology and Child Health top 0.5%
- Prenatal Screening and Diagnostics 20
Genetics top 2%
- Genomic variations and chromosomal abnormalities 12
- Genetic Syndromes and Imprinting 3
Public Health, Environmental and Occupational Health top 2%
- Down syndrome and intellectual disability research 3
Reproductive Medicine top 5%
Molecular Biology top 10%
- DNA Repair Mechanisms 3
- Epigenetics and DNA Methylation 3
Epidemiology
- Congenital Heart Disease Studies 4
Plant Science
- Chromosomal and Genetic Variations 3

Co-authors: Stephanie L. Sherman Emily G. Allen Terry Hassold Lisa F. Taft Lora Bean Dorothy Pettay Kenneth J. Dooley S. L. Sherman
Cited by: Pediatrics, Perinatology and Child Health Genetics Public Health, Environmental and Occupational Health
Journals: Nature Genetics (1 paper)Development (1 paper)The American Journal of Human Genetics (1 paper)
Partner nations: United States Denmark Canada

In The Last Decade

Sallie B. Freeman

28 papers receiving 2.4k citations

Peers

Countries citing papers authored by Sallie B. Freeman

Since Specialization

Citations

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

Fields of papers citing papers by Sallie B. Freeman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Sallie B. Freeman, 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 Sallie B. Freeman Line = papers co-authored together Sallie B. Freeman links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project Genetics in Medicine ·Jessica Ezzell Hunter,Emily G. Allen,Mikyong Shin,Lora Jh Bean,Adolfo Correa,Charlotte M. Druschel,Charlotte A. Hobbs,Leslie A. O’Leary,Paul A. Romitti,Marjorie H. Royle,Claudine P. Torfs,Sallie B. Freeman,Stephanie L. Sherman	2013	40
2	Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: A report from the National Down Syndrome Project Birth Defects Research Part A Clinical and Molecular Teratology ·Lora Jh Bean,Emily G. Allen,Stuart W. Tinker,NaTasha D. Hollis,Adam E. Locke,Charlotte M. Druschel,Charlotte A. Hobbs,Leslie A. O’Leary,Paul A. Romitti,Marjorie H. Royle,Claudine P. Torfs,Kenneth J. Dooley,Sallie B. Freeman,Stephanie L. Sherman	2011	46
3	Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome Genetic Epidemiology ·Adam E. Locke,Kenneth J. Dooley,Stuart W. Tinker,Soo Yeon Cheong,Eleanor Feingold,Emily G. Allen,Sallie B. Freeman,Claudine P. Torfs,L. Clifford,Michael P. Epstein,Michael C. Wu,Xihong Lin,George Capone,Stephanie L. Sherman,Lora Jh Bean	2010	63
4	Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project Genetics in Medicine ·Sallie B. Freeman,Lora Bean,Emily G. Allen,Stuart W. Tinker,Adam E. Locke,Charlotte M. Druschel,Charlotte A. Hobbs,Paul A. Romitti,Marjorie H. Royle,Claudine P. Torfs,Kenneth J. Dooley,Stephanie L. Sherman	2008	204
5	Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects Human Genetics ·Emily G. Allen,Sallie B. Freeman,Charlotte M. Druschel,Charlotte A. Hobbs,Leslie A. O’Leary,Paul A. Romitti,Marjorie H. Royle,Claudine P. Torfs,Stephanie L. Sherman	2008	127
6	Epidemiology of Down syndrome Mental Retardation and Developmental Disabilities Research Reviews ·Stephanie L. Sherman,Emily G. Allen,Lora Bean,Sallie B. Freeman	2007	343
7	Nondisjunction of chromosome 21 American Journal of Medical Genetics ·Norma T. Takaesu,Patricia A. Jacobs,Annette E. Cockwell,R. Dwain Blackston,Sallie B. Freeman,Jelica Nuccio,David M. Kurnit,Irene A. Uchida,Viola Freeman,Terry Hassold	2005	15
8	Linkage disequilibrium mapping in trisomic populations: Analytical approaches and an application to congenital heart defects in Down syndrome Genetic Epidemiology ·Kimberly F. Kerstann,Eleanor Feingold,Sallie B. Freeman,Lora Jh Bean,Robert E. Pyatt,Stuart W. Tinker,Amy H. Jewel,George Capone,Stephanie L. Sherman	2004	14
9	Women with a Reduced Ovarian Complement May Have an Increased Risk for a Child with Down Syndrome The American Journal of Human Genetics ·Sallie B. Freeman,Quanhe Yang,Katherine Allran,Lisa F. Taft,Stephanie L. Sherman	2000	92
10	Risk factors for trisomy 21: Maternal cigarette smoking and oral contraceptive use in a spopulation-based case-control study Genetics in Medicine ·Quanhe Yang,Stephanie L. Sherman,Terry Hassold,Katherine Allran,Lisa F. Taft,Dorothy Pettay,Muin J. Khoury,J. David Erickson,Sallie B. Freeman	1999	71
11	Asplenia syndrome in a child with a balanced reciprocal translocation of chromosomes 11 and 20 [46,XX,t(11;20)(q13.1;q13.13)] American Journal of Medical Genetics ·Sallie B. Freeman,Kasinathan Muralidharan,Dorothy Pettay,R. Dwain Blackston,Kristin M. May	1996	16
12	Susceptible chiasmate configurations of chromosome 21 predispose to non–disjunction in both maternal meiosis I and meiosis II Nature Genetics ·Neil E. Lamb,Sallie B. Freeman,Amanda Savage-Austin,Dorothy Pettay,Lisa F. Taft,Jane Hersey,Yuan-chao Gu,Joseph Shen,Denise M. Saker,Kristen M. May,Dimitris Avramopoulos,Michael B. Petersen,Anni Hallberg,Margareta Mikkelsen,Terry Hassold,Stephanie L. Sherman	1996	290
13	Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study. PubMed ·Paula W. Yoon,Sallie B. Freeman,S. L. Sherman,Lisa F. Taft,Yan Gu,Dorothy Pettay,W. Dana Flanders,Muin J. Khoury,Terry Hassold	1996	145
14	Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination Human Molecular Genetics ·Stephanie L. Sherman,Michael B. Petersen,Sallie B. Freeman,Jane Hersey,Dorothy Pettay,Lisa F. Taft,Merete Frantzen,Margareta Mikkelsen,Terry Hassold	1994	141
15	Paternal uniparental disomy in a child with a balanced 15;15 translocation and Angelman syndrome American Journal of Medical Genetics ·Sallie B. Freeman,Kristin M. May,Dorothy Pettay,Paul M. Fernhoff,Terry Hassold	1993	47
16	Characterization and molecular analysis of nondisjunction in 18 cases of trisomy 21 and leukemia Genes Chromosomes and Cancer ·Briana J. Lorber,Sallie B. Freeman,Terry Hassold,Abdel Ragab,Roger A. Vega,Annette E. Cockwell,Patricia A. Jacobs,Martin Radford,John Doyle,Ian D. Dubé,Alvin Zipursky	1992	17
17	Molecular studies of non-disjunction in trisomy 16. Journal of Medical Genetics ·Terry Hassold,Dorothy Pettay,Sallie B. Freeman,M Grantham,Norma T. Takaesu	1991	52
18	Assignment of X-linked hydrocephalus to Xq28 by linkage analysis Genomics ·Patrick J. Willems,Irene Dijkstra,Bart Van Der Auwera,Lieve Vits,Paul Coucke,Peter Raeymaekers,Christine Van Broeckhoven,G. Giacomo Consalez,Sallie B. Freeman,Stephen T. Warren,Oebele F. Brouwer,Han G. Brunner,W.O. Renier,August F. Van Elsen,Jan E. Dumon	1990	48
19	Prenatal ascertainment of triploidy by maternal serum alpha‐fetoprotein screening Prenatal Diagnosis ·Sallie B. Freeman,Jean H. Priest,Wendy MacMahon,Paul M. Fernhoff,Louis J. Elsas	1989	10
20	SIALIC ACID IN EGG CAPSULES AND OVIDUCTS OF THE NEWT, NOTOPHTHALMUS VIRIDESCENS Biological Bulletin ·Adam Humphries,Sallie B. Freeman,Wilton M. Workman	1968	15

About Sallie B. Freeman

Sallie B. Freeman is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Physiology, having authored 28 papers that have together received 2.5k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (20 papers), Genomic variations and chromosomal abnormalities (12 papers), Congenital Heart Disease Studies (4 papers), Down syndrome and intellectual disability research (3 papers), Genetic Syndromes and Imprinting (3 papers), DNA Repair Mechanisms (3 papers), Epigenetics and DNA Methylation (3 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (1.2k citations), Genetics (963 citations) and Public Health, Environmental and Occupational Health (756 citations). Sallie B. Freeman has collaborated with scholars based in United States, Denmark and Canada. Frequent co-authors include Stephanie L. Sherman, Emily G. Allen, Terry Hassold, Lisa F. Taft, Lora Bean, Dorothy Pettay, Kenneth J. Dooley, S. L. Sherman, Claudine P. Torfs and Charlotte M. Druschel. Their work appears in journals such as Nature Genetics, Development and The American Journal of Human 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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