S. Sherman

J. Greenberg, Jinkuk Hong, S. Sherman, 2014, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Examination of reproductive aging milestones among women who carry the FMR1 premutation.

M. Epstein, S. Sherman, K. Charen, 2007, Human reproduction.

Ovarian histopathological and ubiquitin‐immunophenotypic features in fragile X‐associated primary ovarian insufficiency: a study of five cases and selected controls

M. Gearing, C. Welt, S. Sherman, 2011, Histopathology.

Reproductive Health of Adolescent Girls Who Carry the FMR1 Premutation

S. Sherman, C. Domínguez, JOHN J. DE CARO, 2008, Annals of the New York Academy of Sciences.

Premature ovarian failure among fragile X premutation carriers: parent-of-origin effect?

S. Sherman, 2000, American journal of human genetics.

Comparison of COVID-19 and Non-COVID-19 Pneumonia in Down Syndrome

M. Mayer, M. Dierssen, R. de la Torre, 2021, Journal of clinical medicine.

Study of telomere length in men who carry a fragile X premutation or full mutation allele

P. Chopra, S. Sherman, I. Albizua, 2020, Human Genetics.

Women who carry a fragile X premutation are biologically older than noncarriers as measured by telomere length

S. Sherman, I. Albizua, E. Allen, 2017, American journal of medical genetics. Part A.

Examination of FMR1 transcript and protein levels among 74 premutation carriers

Tiffany R. Oliver, S. Sherman, E. Allen, 2010, Journal of Human Genetics.

Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.

J. Mowrey, S. Warren, S. Sherman, 2009, American journal of human genetics.

Attendance at Fragile X Specialty Clinics: Facilitators and Barriers.

R. Clark, S. Kidd, M. Raspa, 2017, American journal on intellectual and developmental disabilities.

Anti-Mullerian hormone indicates early ovarian decline in fragile X mental retardation (FMR1) premutation carriers: a preliminary study.

S. Sherman, K. Charen, E. Allen, 2008, Human reproduction.

Detection of early FXTAS motor symptoms using the CATSYS computerised neuromotor test battery

R. Letz, S. Sherman, J. Juncos, 2008, Journal of Medical Genetics.

Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction.

L. Shaffer, S. Page, S. Sherman, 2003, American Journal of Human Genetics.

CGG‐repeat polymorphism of the BCR gene rules out predisposing alleles leading to the philadelphia chromosome

G. Riggins, S. Warren, W. Stock, 1994, Genes, chromosomes & cancer.

Trisomy 21: association between reduced recombination and nondisjunction.

P. Jacobs, T. Hassold, M. Mikkelsen, 1991, American journal of human genetics.

Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns

P. Jacobs, T. Hassold, P. Rogan, 1994, Human Genetics.

An n-allele model for progressive amplification in the FMR1 locus.

N. Morton, A. Morris, A. Collins, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Clinical significance of tri-nucleotide repeats in Fragile X testing: A clarification of American College of Medical Genetics guidelines

E. Spector, S. Sherman, K. Kronquist, 2008, Genetics in Medicine.

Recommendations from Multi-disciplinary Focus Groups on Cascade Testing and Genetic Counseling for Fragile X-associated Disorders

Sufen Chiu, D. Hessl, L. Nelson, 2007, Journal of Genetic Counseling.

Recommendations from Multi-disciplinary Focus Groups

Sufen Chiu, D. Hessl, L. Nelson, 2007 .

FMR1 and the continuum of primary ovarian insufficiency.

C. Welt, S. Sherman, Shannon D. Sullivan, 2011, Seminars in reproductive medicine.

Health knowledge of women with a fragile X premutation: Improving understanding with targeted educational material

S. Sherman, K. Charen, Liana Smolich, 2020, Journal of genetic counseling.

Descriptive analysis of seizures and comorbidities associated with fragile X syndrome

S. Warren, J. Sweeney, W. Kaufmann, 2022, Molecular genetics & genomic medicine.

A PCR-based genetic map for human chromosome 3.

J. Weissenbach, P. O'Connell, L. Ballard, 1994, Genomics.

Genetic Analysis Workshop 7: summary of the melanoma workshop.

N. Risch, S. Sherman, 1992, Cytogenetics and cell genetics.

Association between telomere length and chromosome 21 nondisjunction in the oocyte

S. Sherman, I. Albizua, E. Allen, 2015, Human Genetics.

Co‐occurrence of congenital anomalies by maternal race/ethnicity among infants and fetuses with Down syndrome, 2013–2017: A U.S. population‐based analysis

R. Kirby, S. Sherman, P. Lupo, 2021, Birth defects research.

A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiency.

N. Morton, M. New, P. Speiser, 1988, American journal of human genetics.

Abstracts of workshop presentations pp. 1106-1116

R. L. Miller, D. Cox, D. Ledbetter, 1989 .

Study of telomere length in men who carry a fragile X premutation or full mutation allele

P. Chopra, S. Sherman, I. Albizua, 2020, Human Genetics.

Variation in the Zinc Finger of PRDM9 is Associated with the Absence of Recombination along Nondisjoined Chromosomes 21 of Maternal Origin

Tiffany R. Oliver, E. Feingold, Candace D. Middlebrooks, 2016, Journal of Down Syndrome & chromosome abnormalities.

FXPOI: Pattern of AGG Interruptions Does not Show an Association With Age at Amenorrhea Among Women With a Premutation

S. Nolin, S. Sherman, K. Charen, 2018, Front. Genet..

The FMR1 Premutation and Attention-Deficit Hyperactivity Disorder (ADHD): Evidence for a Complex Inheritance

M. Epstein, J. Hunter, S. Sherman, 2012, Behavior genetics.

The diagnostic experience of women with fragile X–associated primary ovarian insufficiency (FXPOI)

S. Sherman, C. Bellcross, E. Allen, 2022, Journal of Assisted Reproduction and Genetics.

Refining the risk for fragile X–associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size

S. Nolin, S. Sherman, K. Charen, 2021, Genetics in Medicine.

Down syndrome

S. Antonarakis, M. Rafii, R. Reeves, 2020, Nature Reviews Disease Primers.

Smarter clustering methods for SNP genotype calling

Yan Lin, George C. Tseng, Eleanor Feingold, 2008, Bioinform..

Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndrome

T. Hassold, S. Sherman, J. Shen, 1998, Chromosoma.

Susceptible chiasmate configurations of chromosome 21 predispose to non–disjunction in both maternal meiosis I and meiosis II

Neil E. Lamb, Stephanie L. Sherman, Lisa Taft, 1996, Nature Genetics.

Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome.

R. Rozen, M. Pogribna, S. J. James, 2000, American journal of human genetics.

Risk factors for trisomy 21: Maternal cigarette smoking and oral contraceptive use in a spopulation-based case-control study

M. Khoury, T. Hassold, Quanhe Yang, 1999, Genetics in Medicine.

Recombination across the centromere of disjoined and non-disjoined chromosome 21.

J. Buard, A. Laurent, G. Roizes, 2003, Human molecular genetics.

Genome-wide variation in recombination in female meiosis: a risk factor for non-disjunction of chromosome 21.

K. Broman, E. Feingold, S. Sherman, 2000, Human molecular genetics.

Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.

E. Feingold, T. Hassold, G. Karadima, 1997, Human molecular genetics.

Recombination and nondisjunction in humans and flies.

R. Hawley, T. Hassold, S. Sherman, 1996, Human molecular genetics.

Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16.

T. Hassold, S. Freeman, S. Sherman, 1995, American Journal of Human Genetics.

Cytogenetic and molecular studies of Down syndrome individuals with leukemia.

P. Jacobs, A. Zipursky, T. Hassold, 1995, American journal of human genetics.

Chapter 3 Trisomy 21: Causes and Consequences

S. Sherman, J. Visootsak, 2008 .

Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans.

M Mikkelsen, T. Hassold, G. Karadima, 1998, Human molecular genetics.

XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region.

D. Page, P. Jacobs, T. Hassold, 1991, American journal of human genetics.

Abstracts for the committee on the genetic constitution of the X chromosome (Part 3 of 3)

Brien, J. Beckmann, K. Kidd, 1991 .

Opportunities, barriers, and recommendations in down syndrome research

Raymond D. Kent, J. Lawrence, S. Warren, 2021, Translational science of rare diseases.

Epidemiology of Down syndrome.

Lora J. H. Bean, Stephanie L Sherman, S. Freeman, 2007, Mental retardation and developmental disabilities research reviews.

Human genes containing polymorphic trinucleotide repeats

G. Riggins, S. Warren, J. L. Chastain, 1992, Nature Genetics.

Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21.

Lora J. H. Bean, V. Cheung, K. Doheny, 2014, Human molecular genetics.

Behavioral genetics '97: ASHG statement. Recent developments in human behavioral genetics: past accomplishments and future directions.

J. Rice, J. Loehlin, J. Meyer, 1997, American journal of human genetics.

Association between maternal age and meiotic recombination for trisomy 21.

E. Feingold, S. Sherman, N. Lamb, 2005, American journal of human genetics.

Germline mutation of microRNA-125a is associated with breast cancer

S. Sherman, F. Kooy, R. Duan, 2009, Journal of Medical Genetics.

Approaches to identify genetic variants that influence the risk for onset of fragile X-associated primary ovarian insufficiency (FXPOI): a preliminary study

S. Sherman, Wendy E. Grus, E. Allen, 2014, Front. Genet..

Maternal Age and Oocyte Aneuploidy: Lessons Learned from Trisomy 21

Lora J. H. Bean, S. Sherman, E. Allen, 2013 .

Genetic Analysis of Variation in Human Meiotic Recombination

Eleanor Feingold, Vivian G. Cheung, Stephanie L. Sherman, 2009, PLoS genetics.

Tight linkage of apolipoprotein C2 to myotonic dystrophy on chromosome 19

M. Pericak-Vance, R. Bartlett, S. Humphries, 1986, Neurology.

A genetic map of chromosome 19 based on family linkage data

S. Sherman, E. Robson, S. Ball, 1985, Annals of human genetics.

Paternal nondisjunction in trisomy 21: excess of male patients.

S. Antonarakis, T. Hassold, M. Petersen, 1993, Human molecular genetics.

Abstracts of workshop presentations (Part 11 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

Startle disease, or hyperekplexia: Response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis

R. Sparkes, S. Sherman, M. Torres, 1992, Annals of neurology.

Recent Developments in Human Behavioral Genetics : Past Accomplishments and Future Directions

J. Loehlin, I. Gottesman, J. Defries, 2007 .

Counting cross-overs: characterizing meiotic recombination in mammals.

P. Hunt, T. Hassold, S. Sherman, 2000, Human molecular genetics.

The marker (X) syndrome: a cytogenetic and genetic analysis

N. Morton, P. Jacobs, G. Turner, 1984, Annals of human genetics.

Fragile X syndrome: Diagnostic and carrier testing

D. Driscoll, B. Pletcher, S. Sherman, 2005, Genetics in Medicine.

Distribution of lod scores under uncertain mode of inheritance.

C. Maclean, D. Bishop, S. Diehl, 1993, American journal of human genetics.

Effect of meiotic recombination on the production of aneuploid gametes in humans

T. Hassold, S. Sherman, N. Lamb, 2005, Cytogenetic and Genome Research.

The FMR1 premutation and reproduction.

C. Welt, L. Nelson, R. Hagerman, 2007, Fertility and sterility.

Parental Perspectives on Pharmacological Clinical Trials: a Qualitative Study in Down Syndrome and Fragile X Syndrome

S. Sherman, J. Visootsak, K. Charen, 2017, Journal of Genetic Counseling.

Expressive language sampling as a source of outcome measures for treatment studies in fragile X syndrome: feasibility, practice effects, test-retest reliability, and construct validity

L. Abbeduto, E. Berry-Kravis, J. Edgin, 2020, Journal of Neurodevelopmental Disorders.

Women with a reduced ovarian complement may have an increased risk for a child with Down syndrome.

Quanhe Yang, S. Freeman, L. Taft, 2000, American journal of human genetics.

Model systems for understanding FXPOI

S. Sherman, R. Hukema, K. Usdin, 2016 .

Fanconi anemia: evidence for linkage heterogeneity on chromosome 20q.

R. G. Allen, A. Auerbach, B. Weiffenbach, 1991, Genomics.

Analytic strategies for stroke genetics.

V. Hertzberg, B. Stern, S. Sherman, 2002, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review

R. Pyeritz, L. Nelson, Y. Cohen, 2018, Front. Genet..

Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice.

P. Jin, Li Lin, Dahua Chen, 2012, Human molecular genetics.

Report of the committee on the genetic constitution of chromosome 1.

G. Bruns, S. Sherman, 1988, Cytogenetics and cell genetics.

Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects

S. Freeman, S. Sherman, P. Romitti, 2009, Human Genetics.

Inherited genetic susceptibility of acute lymphoblastic leukemia in Down syndrome.

Noah A. Kallsen, Shanna A. Peyton, Austin L. Brown, 2019, Blood.

The association between maternal occupation and down syndrome: A report from the national Down syndrome project.

Carissa M Rocheleau, J. Hunter, M. Waters, 2019, International journal of hygiene and environmental health.

Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: A report from the National Down Syndrome Project

Tiffany R. Oliver, Lora J. H. Bean, S. Freeman, 2013, American journal of medical genetics. Part A.

Gestational age is related to symptoms of attention-deficit/hyperactivity disorder in late-preterm to full-term children and adolescents with down syndrome

L. Abbeduto, S. Sherman, Tracie C. Rosser, 2020, Scientific Reports.

Neuropsychiatric and behavioral aspects of trisomy 21

S. Sherman, J. Visootsak, 2007, Current psychiatry reports.

Capturing cognitive and behavioral variability among individuals with Down syndrome: a latent profile analysis

Luther G. Kalb, E. Mahone, R. Reeves, 2021, Journal of neurodevelopmental disorders.

Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome Project.

Lora J. H. Bean, A. Locke, S. Freeman, 2011, Birth defects research. Part A, Clinical and molecular teratology.

Relationship of recombination patterns and maternal age among non-disjoined chromosomes 21.

E. Feingold, S. Sherman, N. Lamb, 2006, Biochemical Society transactions.

Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study.

W D Flanders, M J Khoury, M. Khoury, 1996, American journal of human genetics.

Relationship between Apgar scores and long-term cognitive outcomes in individuals with Down syndrome

D. Harvey, L. Abbeduto, S. Sherman, 2021, Scientific Reports.

Investigation of factors associated with paternal nondisjunction of chromosome 21

Eleanor Feingold, Tiffany R. Oliver, Stephanie L Sherman, 2009, American journal of medical genetics. Part A.

Association of FMR1 repeat size with ovarian dysfunction.

M. Epstein, S. Sherman, E. Allen, 2005, Human reproduction.

Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment

W. Brown, W. Kaufmann, H. Andrews, 2017, Pediatrics.

Fragile X analysis of 1112 prenatal samples from 1991 to 2010

W. Brown, S. Nolin, Nicole Ersalesi, 2011, Prenatal diagnosis.

Abstracts of workshop presentations (Part 1 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles

A. Vianna-Morgante, M. Milá, S. Nolin, 2019, American journal of medical genetics. Part A.

Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population.

D. Crawford, M. Yeargin-Allsopp, C. Boyle, 1999, American journal of human genetics.

Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population.

S. Sherman, D. Pettay, J. Hersey, 1996, American journal of medical genetics.

Fragile X syndrome: examination of issues pertaining to population-based screening

S. Sherman, K. Meadows, 1996 .

Modeling the natural history of the fragile X gene

S. Sherman, 1995 .

Segregation analysis of balanced pericentric inversions in pedigree data

N. Morton, J. Lindsten, M. Petersen, 1986, Clinical genetics.

Recurrence risks for relatives in families with an isolated case of the fragile X syndrome.

G. Turner, S. Sherman, A. Rogatko, 1988, American journal of medical genetics.

Analysis of the genomic expression profile in trisomy 18: insight into possible genes involved in the associated phenotypes.

S. Warren, P. Chopra, M. Gambello, 2019, Human molecular genetics.

Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles.

W. Brown, J. Mandel, H. Hjalgrim, 2003, American journal of human genetics.

Women’s Attitudes Toward Testing for Fragile X Carrier Status: A Qualitative Analysis

L. Taft, S. Sherman, A. Anido, 2005, Journal of Genetic Counseling.

Paternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size range.

D. Crawford, S. Sherman, M. Leslie, 2002, American journal of human genetics.

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

N. E. Morton, P. A. Jacobs, N. Morton, 2004, Human Genetics.

Conference report: Fourth International Workshop on the fragile X and X-linked mental retardation.

K. Davies, W. Brown, H. Lubs, 1988, American journal of medical genetics.

A branching non‐linear autoregressive model for the transmission of the fragile X dynamic repeat mutation

R. Huggins, S. Sherman, D. Loesch, 1998, Annals of human genetics.

The International Fragile X Premutation Registry: building a resource for research and clinical trial readiness

Peter K. Todd, D. Hessl, D. Hall, 2022, Journal of Medical Genetics.

Evolving methods in genetic epidemiology. IV. Approaches to non-Mendelian inheritance.

S. Sherman, 1997, Epidemiologic Reviews.

Regionally Smoothed Meta‐Analysis Methods for GWAS Datasets

George C Tseng, Monir H. Sharker, Ferdouse Begum, 2016, Genetic epidemiology.

Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21

Tiffany R. Oliver, Lora J. H. Bean, V. Cheung, 2012, Human Genetics.

An Examination of the Relationship between Hotspots and Recombination Associated with Chromosome 21 Nondisjunction

Tiffany R. Oliver, Lora J. H. Bean, V. Cheung, 2014, PloS one.

Genetic analysis workshop IV: Summary for coeliac disease

S. Sherman, 1987, Genetic epidemiology. Supplement.

Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR.

D. Crawford, S. Sherman, B. Wilson, 2000, Human molecular genetics.

associated with breast cancer Germline mutation of microRNA-125a is

W. Zhou, S. Sherman, F. Kooy, 2009 .

Consensus characterization of 16 FMR1 reference materials: a consortium study.

Amit Phansalkar, Elaine Lyon, Monique A Johnson, 2008, The Journal of molecular diagnostics : JMD.

The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project

Lora J. H. Bean, A. Correa, J. Hunter, 2013, Genetics in Medicine.

Abstracts of workshop presentations (Part 13 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

Prevalence of the fragile X syndrome in African-Americans.

D. Crawford, M. Yeargin-Allsopp, C. Boyle, 2002, American journal of medical genetics.

Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability.

S. Warren, D. Crawford, S. Sherman, 2000, Human molecular genetics.

Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population.

C. Gunter, A. Reiss, S. Warren, 2000, American journal of human genetics.

Report of the committee on the genetic constitution of chromosome 1.

G. Bruns, S. Sherman, 1989, Cytogenetics and cell genetics.

Linkage disequilibrium mapping in trisomic populations: Analytical approaches and an application to congenital heart defects in Down syndrome

Eleanor Feingold, Lora J H Bean, Lora J. H. Bean, 2004, Genetic epidemiology.

Estimating meiotic exchange patterns from recombination data: an application to humans.

E. Feingold, S. Sherman, N. Lamb, 1997, Genetics.

Bias associated with study protocols in epidemiologic studies of disease familial aggregation.

M. Khoury, W. Flanders, S. Sherman, 2000, American Journal of Epidemiology.

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

N. Morton, M. Pembrey, R. Winter, 2004, Human Genetics.

Familial split hand/split foot long bone deficiency does not segregate with markers linked to the SHFD1 locus in 7q21.3-q22.1.

C. Schwartz, S. Sherman, E. Boyd, 1994, Human molecular genetics.

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.

C. Gunter, D. Nelson, S. Warren, 1998, Human molecular genetics.

Significance of linkage disequilibrium between the fragile X locus and its flanking markers.

G. Neri, P. Chiurazzi, S. Sherman, 1996, American journal of medical genetics.

Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site.

J. Sutcliffe, G. Riggins, D. Nelson, 1992, American journal of medical genetics.

Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects

Michael E Zwick, Lora J H Bean, Lora J. H. Bean, 2017, G3: Genes, Genomes, Genetics.

FISH studies of the sperm of fathers of paternally derived cases of trisomy 21: no evidence for an increase in aneuploidy

T. Hassold, E. Millie, L. Taft, 1998, Human Genetics.

FORWARD: A Registry and Longitudinal Clinical Database to Study Fragile X Syndrome

Sharyn A. Lincoln, W. Kaufmann, E. Berry-Kravis, 2017, Pediatrics.

New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS)

S. Sherman, J. Juncos, L. Shubeck, 2011, neurogenetics.

Down syndrome: national conference on patient registries, research databases, and biobanks.

J. Krischer, S. Terry, P. Kaufmann, 2011, Molecular genetics and metabolism.

An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects.

Lora J. H. Bean, S. Mooney, C. Maslen, 2012, American journal of human genetics.

An empirical bayesian approach for testing gene expression fold change and its application in detecting global dosage effects

Zhaohui S. Qin, Z. Qin, J. Birchler, 2020, NAR genomics and bioinformatics.

The method of sib‐pair linkage analysis in context of case‐control design

M. Khoury, Quanhe Yang, F. Sun, 1997, Genetic epidemiology.

Maternal meiosis II nondisjunction in trisomy 21 is associated with maternal low socioeconomic status

S. Sherman, C. Torfs, R. Christianson, 2004, Genetics in Medicine.

Multipoint estimation of genetic maps for human trisomies with one parent or other partial data.

E Feingold, E. Feingold, S. Sherman, 2000, American journal of human genetics.

Cognitive aspects of Fragile X syndrome.

S. Sherman, J. Visootsak, Lillie Huddleston, 2014, Wiley interdisciplinary reviews. Cognitive science.

The cognitive neuropsychological phenotype of carriers of the FMR1 premutation

S. Rivera, J. Olichney, Jin-Chen Yang, 2014, Journal of Neurodevelopmental Disorders.

Associated features in females with an FMR1 premutation

J. Greenberg, J. Olichney, M. Milá, 2014, Journal of Neurodevelopmental Disorders.

Depression and anxiety symptoms among women who carry the FMR1 premutation: Impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms

E. Binder, J. Cubells, J. Hunter, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Is there evidence for neuropsychological and neurobehavioral phenotypes among adults without FXTAS who carry the FMR1 premutation? A review of current literature

J. Hunter, S. Sherman, A. Abramowitz, 2009, Genetics in Medicine.

Investigation of Phenotypes Associated with Mood and Anxiety Among Male and Female Fragile X Premutation Carriers

J. Hunter, S. Sherman, A. Abramowitz, 2008, Behavior genetics.

Cognitive and behavioral performance among FMR1 high-repeat allele carriers surveyed from special education classes.

J. Bregman, S. Sherman, A. Abramowitz, 2002, American journal of medical genetics.

Analyses stratified by maternal age and recombination further characterize genes associated with maternal nondisjunction of chromosome 21

E. Feingold, S. Sherman, J. Chernus, 2021, Prenatal diagnosis.

Development and validation of the Arizona Cognitive Test Battery for Down syndrome

Melissa J. Allman, Lynn Nadel, Stephanie L. Sherman, 2010, Journal of Neurodevelopmental Disorders.

Spoken language outcome measures for treatment studies in Down syndrome: feasibility, practice effects, test-retest reliability, and construct validity of variables generated from expressive language sampling

L. Abbeduto, E. Berry-Kravis, J. Edgin, 2021, Journal of neurodevelopmental disorders.

Normal variation at the myotonic dystrophy locus in global human populations.

S. Warren, A. Torroni, S. Sherman, 1995, American journal of human genetics.

Abstracts of workshop presentations (Part 12 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

The Arizona Cognitive Test Battery for Down Syndrome: Test-Retest Reliability and Practice Effects.

E. I. Pierpont, C. Maslen, L. Abbeduto, 2017, American journal on intellectual and developmental disabilities.

Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

A J Agopian, Cristina E. Trevino, D. Cutler, 2020, Scientific Reports.

Associations Between Medical History, Cognition, and Behavior in Youth With Down Syndrome: A Report From the Down Syndrome Cognition Project.

E. I. Pierpont, C. Maslen, E. Feingold, 2018, American journal on intellectual and developmental disabilities.

Contribution of Copy Number Variation to Down Syndrome-associated Atrioventricular Septal Defects

Michael E Zwick, Promita Bose, Lora J H Bean, 2014, Genetics in Medicine.

The origin of non-disjunction in humans

T. Hassold, S. Sherman, 1993 .

The Relation of the Dopamine Transporter Gene (DAT1) to Symptoms of Internalizing Disorders in Children

I. Waldman, S. Sherman, A. Abramowitz, 1998, Behavior genetics.

Abstracts of workshop presentations (Part 4 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

Examination of factors associated with instability of the FMR1 CGG repeat.

C. Schwartz, W. Brown, A. Ashley-Koch, 1998, American journal of human genetics.

Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females.

S. Sherman, K. Meadows, A. Ashley, 1996, American journal of medical genetics.

The FMR1 Premutation and Attention-Deficit Hyperactivity Disorder (ADHD): Evidence for a Complex Inheritance

J. Hunter, S. Sherman, A. Abramowitz, 2011, Behavior Genetics.

Intra-individual stability over time of standardized anti-Mullerian hormone in FMR1 premutation carriers.

A. V. van Kessel, A. Smits, T. Feuth, 2011, Human reproduction.

Insufficiency in Mice

P. Jin, Li Lin, Dahua Chen, 2012 .

Reproductive endocrinology Intra-individual stability over time of standardized anti-Müllerian hormone in FMR 1 premutation carriers

A. Smits, T. Feuth, H. Yntema, 2011 .

Decisions to participate in fragile X and other genomics-related research: Native American and African American voices.

S. Sherman, L. Stephens, W. Williams, 2009, Journal of cultural diversity.

No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50.

J. Hunter, S. Sherman, A. Abramowitz, 2008, American journal of human genetics.

Fragile X‐associated primary ovarian insufficiency: evidence for additional genetic contributions to severity

M. Epstein, J. Hunter, S. Sherman, 2008, Genetic epidemiology.

Newborn, Carrier, and Early Childhood Screening Recommendations for Fragile X

W. Brown, W. Kaufmann, D. Skinner, 2012, Pediatrics.

Genetic Diversity of the Fragile X Syndrome Gene (FMR1) in a Large Sub‐Saharan West African Population

S. Sherman, E. Allen, Scott M. Williams, 2010, Annals of human genetics.

Fragile X AGG analysis provides new risk predictions for 45–69 repeat alleles

W. Brown, R. Shroff, F. Tassone, 2013, American journal of medical genetics. Part A.

Genetic Control of Hotspots

V. Cheung, E. Feingold, S. Sherman, 2010, Science.

Characteristics Associated with Autism Spectrum Disorder Risk in Individuals with Down Syndrome

G. Capone, S. Sherman, L. Hahn, 2019, Journal of Autism and Developmental Disorders.

Characteristics Associated with Autism Spectrum Disorder Risk in Individuals with Down Syndrome

G. Capone, S. Sherman, L. Hahn, 2019, Journal of Autism and Developmental Disorders.

Predictors and risk model development for menopausal age in fragile X premutation carriers

A. Smits, T. Feuth, H. Yntema, 2011, Genetics in Medicine.

A counseling guide to the Martin-Bell syndrome.

D. Weaver, S. Sherman, 1987, American journal of medical genetics.

A new genetic model for the fragile X syndrome involving an autosomal suppressor gene--comments on the paper by M.H. Israel.

S. Sherman, 1987, American journal of medical genetics.

FMR1 CGG expansion to full mutation: What is the lower limit in premutation females?

W. Brown, J. Mandel, H. Hjalgrim, 2000 .

Characteristics of the transmission of the FMR1 gene from carrier females in a prospective sample of conceptuses.

C. Schwartz, W. Brown, A. Smits, 1994, American journal of medical genetics.

An application of empirical Bayes methods to updating linkage information on chromosome 21.

B. Keats, K. Amfoh, S. Sherman, 1992, Cytogenetics and cell genetics.

Influence of CHDs on psycho-social and neurodevelopmental outcomes in children with Down syndrome

J. Hunter, A. Perkins, S. Sherman, 2015, Cardiology in the Young.

Clustering of comorbid conditions among women who carry an FMR1 premutation

J. Hunter, S. Sherman, K. Charen, 2020, Genetics in Medicine.

Genomic landscape of Down syndrome-associated acute lymphoblastic leukemia.

M. Loh, M. Shago, J. Gastier-Foster, 2023, Blood.

Report of the committee on linkage and gene order.

B. Keats, S. Sherman, J. Ott, 1990, Cytogenetics and cell genetics.

Improving Health Education for Women Who Carry an FMR1 Premutation

S. Sherman, J. Visootsak, K. Charen, 2016, Journal of Genetic Counseling.

Improved prenatal detection of fra(X)(q27.3): methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures.

S. Sherman, E. Jenkins, S. Kunaporn, 1991, American journal of medical genetics.

Genetic epidemiologic methods to screen for matrilineal inheritance in mitochondrial disorders

D. Wallace, W. Flanders, R. Go, 1996, Genetic epidemiology.

Abstracts of workshop presentations pp. 1075-1091

R. L. Miller, D. Cox, D. Ledbetter, 1989 .

Correction to: Expressive language sampling as a source of outcome measures for treatment studies in fragile X syndrome: feasibility, practice effects, test-retest reliability, and construct validity

L. Abbeduto, E. Berry-Kravis, J. Edgin, 2020, Journal of Neurodevelopmental Disorders.

Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: heterogeneity owing to diagnostic subtype and severity.

I. Waldman, S. Sherman, D. Rowe, 1998, American journal of human genetics.

Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation

Cristina E. Trevino, D. Cutler, M. Epstein, 2021, Fertility and sterility.

Contributors and Participants

D. Cox, A. Kong, N. Mendell, 1982 .

Investigation of factors associated with paternal nondisjunction of chromosome 21

Tiffany R. Oliver, E. Feingold, S. Sherman, 2009 .

A novel procedure for genotyping of single nucleotide polymorphisms in trisomy with genomic DNA and the invader assay

Michael Olivier, Adam Locke, Jack Littrell, 2008, Nucleic acids research.

Abstracts of workshop presentations pp. 1057-1074

R. L. Miller, D. Cox, D. Ledbetter, 1989 .

Predictors of Comorbid Conditions in Women Who Carry an FMR1 Premutation

J. Hunter, S. Sherman, K. Charen, 2021, Frontiers in Psychiatry.

Abstracts for the committee on the genetic constitution of chromosome 6

Brien, J. Beckmann, K. Kidd, 1991 .

Abstracts of workshop presentations pp. 1023-1039

R. L. Miller, D. Cox, D. Ledbetter, 1989 .

Abstracts for the committee on comparative gene mapping

Brien, J. Beckmann, K. Kidd, 1991 .

Multipoint genetic mapping with trisomy data.

H. Zhao, S. Sherman, N. Lamb, 2001, American journal of human genetics.

A Variance-Component Framework for Pedigree Analysis of Continuous and Categorical Outcomes

Xihong Lin, M. Boehnke, M. Epstein, 2009, Statistics in biosciences.

Response to Stene's comments on the segregation of balanced pericentric inversions

L. Iselius, S. Sherman, 1986, Clinical genetics.

Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts.

J. Grigsby, K. Cornish, C. Kogan, 2012, Neuropsychology.

Abstracts for the committee on the genetic constitution of chromosome 15

Brien, J. Beckmann, K. Kidd, 1991 .

Feasibility of an app-based mindfulness intervention among women with an FMR1 premutation experiencing maternal stress.

Stephanie L Sherman, Charisma L. Jenkins, Jessica Ezzell Hunter, 2019, Research in developmental disabilities.

Depression and anxiety symptoms among women who carry the FMR1 premutation: Impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms

E. Binder, J. Cubells, J. Hunter, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50.

J. Hunter, S. Sherman, A. Abramowitz, 2008, American journal of human genetics.

Neurodevelopmental outcomes in children with Down syndrome and congenital heart defects

P. Kirshbom, W. Mahle, S. Sherman, 2011, American journal of medical genetics. Part A.

Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects

Lora J. H. Bean, D. Cutler, C. Maslen, 2015, G3: Genes, Genomes, Genetics.

Epidemiology of Down syndrome.

Lora J. H. Bean, S. Freeman, S. Sherman, 2007, Mental retardation and developmental disabilities research reviews.

Genotype/Phenotype Relationships in FXTAS

F. Tassone, S. Sherman, M. Leehey, 2010 .

Low-level maternal exposure to nicotine associates with significant metabolic perturbations in second-trimester amniotic fluid.

Dean P. Jones, C. Schwartz, Shuzhao Li, 2017, Environment international.