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1

Down syndrome

Antonarakis, Stylianos E., Skotko, Brian G., Rafii, Michael S., Strydom, Andre, Pape, Sarah E., Bianchi, Diana W., Sherman, Stephanie L., Reeves, Roger H.

Journal:

Nature Reviews Disease Primers

Year:

2020

Language:

english

File:

PDF, 3.25 MB

english, 2020

2

Caffeine Enhances Memory Performance in Young Adults during Their Non-optimal Time of Day

Sherman, Stephanie M., Buckley, Timothy P., Baena, Elsa, Ryan, Lee

Journal:

Frontiers in Psychology

Year:

2016

Language:

english

File:

PDF, 839 KB

english, 2016

3

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

Emily Graves Allen, Sallie B. Freeman, Charlotte Druschel, Charlotte A. Hobbs, Leslie A. O’Leary, Paul A. Romitti, Marjorie H. Royle, Claudine P. Torfs, Stephanie L. Sherman

Journal:

Year:

2009

Language:

english

File:

PDF, 470 KB

english, 2009

4

Religious Coping and Posttraumatic Growth Among Family Caregivers of Cancer Patients in India

Thombre, Avinash, Sherman, Allen C., Simonton, Stephanie

Journal:

Journal of Psychosocial Oncology

Year:

2010

Language:

english

File:

PDF, 135 KB

english, 2010

5

Covid-19 lockdowns, income distribution, and food security: An analysis for South Africa

Arndt, Channing, Davies, Rob, Gabriel, Sherwin, Harris, Laurence, Makrelov, Konstantin, Robinson, Sherman, Levy, Stephanie, Simbanegavi, Witness, van Seventer, Dirk, Anderson, Lillian

Journal:

Global Food Security

Year:

2020

File:

PDF, 1.23 MB

2020

6

Safety Factors Predictive of Job Satisfaction and Job Retention Among Home Healthcare Aides

Sherman, Martin F., Gershon, Robyn R. M., Samar, Stephanie M., Pearson, Julie M., Canton, Allison N., Damsky, Marc R.

Journal:

Journal of Occupational & Environmental Medicine

Year:

2008

Language:

english

File:

PDF, 472 KB

english, 2008

7

Epidemiology of Down syndrome

Stephanie L. Sherman, Emily G. Allen, Lora H. Bean, Sallie B. Freeman

Journal:

Development Diabilities Research Reviews

Year:

2007

Language:

english

File:

PDF, 153 KB

english, 2007

8

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

Sherman, Stephanie L., Meadows, Kellen L., Ashley, Allison E.

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 532 KB

english, 1996

9

Policy Statement: American college of medical genetics. Fragile X Syndrome: Diagnostic and carrier testing

Vicki Park, Patricia Howard-Peebles, Stephanie Sherman, Annette Taylor, Eric Wulfsberg

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 227 KB

english, 1994

10

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

M. Hixon, Elise Millie, L. A. Judis, Stephanie Sherman, Katherine Allran, Lisa Taft, Terry Hassold

Journal:

Year:

1998

Language:

english

File:

PDF, 40 KB

english, 1998

11

Posttraumatic growth among cancer patients in India

Avinash Thombre, Allen C. Sherman, Stephanie Simonton

Journal:

Journal of Behavioral Medicine

Year:

2010

Language:

english

File:

PDF, 226 KB

english, 2010

12

Neuropsychiatric and behavioral aspects of trisomy 21

Jeannie Visootsak, Stephanie Sherman

Journal:

Current Psychiatry Reports

Year:

2007

Language:

english

File:

PDF, 214 KB

english, 2007

13

Association between Maternal Age and Meiotic Recombination for Trisomy 21

Neil E. Lamb, Kai Yu, John Shaffer, Eleanor Feingold, Stephanie L. Sherman

Journal:

The American Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 1.70 MB

english, 2005

14

Diagnosis of Fragile X Syndrome: A Qualitative Study of African American Families

Visootsak, Jeannie, Charen, Krista, Rohr, Julia, Allen, Emily, Sherman, Stephanie

Journal:

Journal of Genetic Counseling

Year:

2012

Language:

english

File:

PDF, 159 KB

english, 2012

15

The fading affect bias across alcohol consumption frequency for alcohol-related and non-alcohol-related events

Gibbons, Jeffrey A., Toscano, Angela, Kofron, Stephanie, Rothwell, Christine, Lee, Sherman A., Ritchie, Timothy D., Walker, W. Richard

Journal:

Consciousness and Cognition

Year:

2013

Language:

english

File:

PDF, 532 KB

english, 2013

16

A Working Daigram of the Visual Arts Organizing Field

Sherman, Stephanie, Sokolow, Deb

Journal:

Year:

2015

Language:

english

File:

PDF, 11.39 MB

english, 2015

17

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

Kaufmann, Walter E., Kidd, Sharon A., Andrews, Howard F., Budimirovic, Dejan B., Esler, Amy, Haas-Givler, Barbara, Stackhouse, Tracy, Riley, Catharine, Peacock, Georgina, Sherman, Stephanie L., Brown,

Journal:

Year:

2017

Language:

english

File:

PDF, 549 KB

english, 2017

18

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

Albizua, Igor, Chopra, Pankaj, Sherman, Stephanie L, Gambello, Michael J, Warren, Stephen T

Journal:

Human Molecular Genetics

Year:

2019

File:

PDF, 605 KB

2019

19

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

Abbeduto, Leonard, Berry-Kravis, Elizabeth, Sterling, Audra, Sherman, Stephanie, Edgin, Jamie O., McDuffie, Andrea, Hoffmann, Anne, Hamilton, Debra, Nelson, Michael, Aschkenasy, Jeannie, Thurman, Ange

Journal:

Journal of Neurodevelopmental Disorders

Year:

2020

File:

PDF, 191 KB

2020

20

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

Meadows, Kellen L., Pettay, Dorothy, Newman, James, Hersey, Jane, Ashley, Allison E., Sherman, Stephanie L.

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 564 KB

english, 1996

21

Population-based study of congenital heart defects in Down syndrome

Freeman, Sallie B., Taft, Lisa F., Dooley, Kenneth J., Allran, Katherine, Sherman, Stephanie L., Hassold, Terry J., Khoury, Muin J., Saker, Denise M.

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 114 KB

english, 1998

22

Genetic epidemiologic methods to screen for matrilineal inheritance in mitochondrial disorders

Fatima Mili, W. Dana Flanders, Stephanie L. Sherman, Rodney C.P. Go, Douglas C. Wallace

Journal:

Genetic Epidemiology

Year:

1996

Language:

english

File:

PDF, 695 KB

english, 1996

23

Sequential sib-pair and association studies to detect genes in quantitative traits

Amanda Savage, Fengzhu Sun, Dana C. Crawford, Allison E. Ashley, Quanhe Yang, Stephanie L. Sherman

Journal:

Genetic Epidemiology

Year:

1997

Language:

english

File:

PDF, 34 KB

english, 1997

24

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

Quanhe Yang, Michael Atkinson, Fengzhu Sun, Stephanie Sherman, Muin J. Khoury

Journal:

Genetic Epidemiology

Year:

1997

Language:

english

File:

PDF, 29 KB

english, 1997

25

Testing for contributions of mitochondrial DNA mutations to complex diseases

Fengzhu Sun, Allison E. Ashley-Koch, L. Kathryn Durham, Eleanor Feingold, M. Elizabeth Halloran, Amita K. Manatunga, Stephanie L. Sherman

Journal:

Genetic Epidemiology

Year:

1998

Language:

english

File:

PDF, 131 KB

english, 1998

26

Premature ovarian failure in the fragile X syndrome

Stephanie L. Sherman

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 120 KB

english, 2000

27

Small encapsulated hepatocellular carcinoma of the liver provisional analysis of pathogenetic mechanisms

Ross G. Cameron, Emmanuel Farber, M. James Phillips, Paul D. Greig, Stephanie Wilson, Morris Sherman, Gary A. Levy

Journal:

Year:

1993

Language:

english

File:

PDF, 1.45 MB

english, 1993

28

Coping with head and neck cancer during different phases of treatment

Allen C. Sherman, Stephanie Simonton, Dawn Camp Adams, Emre Vural, Ehab Hanna

Journal:

Year:

2000

Language:

english

File:

PDF, 115 KB

english, 2000

29

Prevalence of the fragile X syndrome in African-Americans

Dana C. Crawford, Kellen L. Meadows, James L. Newman, Lisa F. Taft, Elizabeth Scott, Mary Leslie, Lisa Shubek, Patricia Holmgreen, Marshalyn Yeargin-Allsopp, Coleen Boyle, Stephanie L. Sherman

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 83 KB

english, 2002

30

The fragile(X) syndrome: The mutation problem

Patricia A. Jacobs, Stephanie Sherman, Gillian Turner, Tessa Webb, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 362 KB

english, 1986

31

A counseling guide to the Martin-Bell syndrome

David D. Weaver, Stephanie L. Sherman, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 273 KB

english, 1987

32

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

Dr. Stephanie L. Sherman

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 351 KB

english, 1987

33

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

Stephanie L. Sherman, André Rogatko, Gillian Turner, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1988

Language:

english

File:

PDF, 722 KB

english, 1988

34

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

Dr. W. Ted Brown, Ed Jenkins, Giovanni Neri, Herbert Lubs, Lawrence R. Shapiro, Kay E. Davies, Stephanie Sherman, Randi Hagerman, Charles Laird

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 2.33 MB

english, 1991

35

Collaborative prospective study of the fragile X syndrome: Request for participation

Stephanie L. Sherman

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 401 KB

english, 1991

36

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

Edmund C. Jenkins, Michael S. Krawczun, Sandra L. Stark-Houck, Charlotte J. Duncan, Suphat Kunaporn, Hong Gu, Carol Schwartz-Richstein, Patricia N. Howard-Peebles, Anne Gross, Stephanie L. Sherman, W.

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 534 KB

english, 1991

37

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

Gregory J. Riggins, Stephanie L. Sherman, Ben A. Oostra, James S. Sutcliffe, David Feitell, David L. Nelson, Bernard A. Van Oost, Arie P. T. Smits, Feliciano J. Ramos, Ellen Pfendner, Derek P. A. Kuhl

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 529 KB

english, 1992

38

Concordance and recessive inheritance of Leber congenital amaurosis

Scott R. Lambert, Stephanie Sherman, David Taylor, Anthony Kriss, Rebecca Coffey, Marcus Pembrey

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 271 KB

english, 1993

39

CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defects in Down syndrome

Cheryl L. Maslen, Darcie Babcock, Susan W. Robinson, Lora J. H. Bean, Kenneth J. Dooley, Virginia L. Willour, Stephanie L. Sherman

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 117 KB

english, 2006

40

Neurodevelopmental outcomes in children with Down syndrome and congenital heart defects

Jeannie Visootsak, William T. Mahle, Paul M. Kirshbom, Lillie Huddleston, Marcia Caron-Besch, Amy Ransom, Stephanie L. Sherman

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 98 KB

english, 2011

41

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

Dr Stephen G. Ryan, Stephanie L. Sherman, Joseph C. Terry, Robert S. Sparkes, M. Cristina Torres, Ray W. Mackey

Journal:

Annals of Neurology

Year:

1992

Language:

english

File:

PDF, 711 KB

english, 1992

42

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

Gregory J. Riggins, Stephen T. Warren, Stephanie L Sherman, Carol N. Phillips, Wendy Stock, Carol A. Westbrook

Journal:

Genes, Chromosomes and Cancer

Year:

1994

Language:

english

File:

PDF, 357 KB

english, 1994

43

A trisomic transmission disequilibrium test

Zhiying Xu, Kimberly F. Kerstann, Stephanie L. Sherman, Aravinda Chakravarti, Eleanor Feingold

Journal:

Genetic Epidemiology

Year:

2004

Language:

english

File:

PDF, 86 KB

english, 2004

44

Combined segregation and linkage analysis for IDDM and HLA-DR under several ascertainment assumptions

Leigh Pascoe, Stephanie Sherman, Danny Wu, Murray Becker, Catherine Falk

Journal:

Genetic Epidemiology

Year:

1989

Language:

english

File:

PDF, 389 KB

english, 1989

45

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

Kimberly F. Kerstann, Eleanor Feingold, Sallie B. Freeman, Lora J. H. Bean, Robert Pyatt, Stuart Tinker, Amy H. Jewel, George Capone, Stephanie L. Sherman

Journal:

Genetic Epidemiology

Year:

2004

Language:

english

File:

PDF, 157 KB

english, 2004

46

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

Jessica Ezzell Hunter, Michael P. Epstein, Stuart W. Tinker, Krista H. Charen, Stephanie L. Sherman

Journal:

Genetic Epidemiology

Year:

2008

Language:

english

File:

PDF, 99 KB

english, 2008

47

Postoperative radiotherapy for advanced medullary thyroid cancer—Local disease control in the modern era

David L. Schwartz, Vishal Rana, Stephanie Shaw, Cynthia Yazbeck, Kie-Kian Ang, William H. Morrison, David I. Rosenthal, Ana Hoff, Douglas B. Evans, Gary L. Clayman, Adam S. Garden, Steven I. Sherman

Journal:

Year:

2008

Language:

english

File:

PDF, 215 KB

english, 2008

48

Interaction between a chromosome 10 RET enhancer and chromosome 21 in the Down syndrome–Hirschsprung disease association

Stacey Arnold, Anna Pelet, Jeanne Amiel, Salud Borrego, Robert Hofstra, Paul Tam, Isabella Ceccherini, Stanislas Lyonnet, Stephanie Sherman, Aravinda Chakravarti

Journal:

Year:

2009

Language:

english

File:

PDF, 274 KB

english, 2009

49

Down syndrome: genetic recombination and the origin of the extra chromosome 21

Terry Hassold, Stephanie Sherman

Journal:

Clinical Genetics

Year:

2000

Language:

english

File:

PDF, 144 KB

english, 2000

50

Fragile X analysis of 1112 prenatal samples from 1991 to 2010

Sarah L. Nolin, Anne Glicksman, Xiaohua Ding, Nicole Ersalesi, W. Ted Brown, Stephanie L. Sherman, Carl Dobkin

Journal:

Prenatal Diagnosis

Year:

2011

Language:

english

File:

PDF, 123 KB

english, 2011