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S

Suzanne B. Cassidy

University of California System

42H指数
185论文数
1.0W被引数
收录论文 21
发表时间
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Letter regarding Prevalence of growth hormone deficiency in previously GH-treated young adults with Prader-Willi syndrome by Donze et al
errCLINICAL ENDOCRINOLOGY
IF2.4
err2019-06-26
err5
PREAI
errHoybye, Charlotte; Tauber, Maithe; Angulo, Moris A.; Eiholzer, Urs; Driscoll, Daniel J.; Cassidy, Suzanne B.; Holland, Antony J.
err分享
err收藏
Clinical utility gene card for: Prader-Willi Syndrome
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2014-04-16
err21
errOAAI
errBuiting, Karin; Cassidy, Suzanne B.; Driscoll, Daniel J.; Gillessen-Kaesbach, Gabriele; Kanber, Deniz; Tauber, Maithe; Schwinger, Eberhard; Horsthemke, Bernhard
err分享
err收藏
Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology
errGENETICS IN MEDICINE
IF6.2
err2014-02-01
err18
errOAAI
errGold, June-Anne; Ruth, Chelsey; Osann, Kathryn; Flodman, Pamela; McManus, Barbara; Lee, Hye-Seung; Donkervoort, Sandra; Khare, Manaswitha; Roof, Elizabeth; Dykens, Elizabeth; Driscoll, Daniel J.; Butler, Merlin G.; Heinemann, Janalee; Cassidy, Suzanne; Kimonis, Virginia E.
err分享
err收藏
Prader-Willi syndrome
errGENETICS IN MEDICINE
IF6.2
err2012-01-01
err1.0K
errOAAI
errCassidy, Suzanne B.; Schwartz, Stuart; Miller, Jennifer L.; Driscoll, Daniel J.
err分享
err收藏
Associations between serum 25-hydroxyvitamin D, parathyroid hormone and osteocalcin in a representative sample of Irish adults aged ≥ 18 years
errPROCEEDINGS OF THE NUTRITION SOCIETY
IF4.5
err2011-08-15
err0
errOAAI
errCassidy, S.; Muldowney, S.; Walsh, E.; Walton, J.; McNulty, B.; Nugent, A.; Gibney, M. J.; Flynn, A.; Cashman, K. D.
err分享
err收藏
Prader-Willi and Angelman syndromes: genetic counseling Reply
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2009-10-07
err0
errOAAI
errCassidy, Suzanne B.; Driscoll, Daniel J.
err分享
err收藏
Prader-Willi syndrome
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2008-09-10
err493
errOAAI
errCassidy, Suzanne B.; Driscoll, Daniel J.
err分享
err收藏
Obsessions and compulsions in Prader-Willi syndrome
errJOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY
IF7
err2006-12-07
err230
PREAI
errDykens, EM; Leckman, JF; Cassidy, B
err分享
err收藏
Terminal 22q deletion syndrome: A newly recognized cause of speech and language disability in the autism spectrum终端22q缺失综合征: 自闭症谱系中言语和语言残疾的新认识原因
errPEDIATRICS
IF6.4
err2004-08-01
err156
PREAI
errManning, MA; Cassidy, SB; Clericuzio, C; Cherry, AM; Schwartz, S; Hudgins, L; Enns, GM; Hoyme, HE
err分享
err收藏
Delineation of complex chromosomal rearrangements: evidence for increased complexity
errHUMAN GENETICS
IF3.6
err2004-04-01
err27
PREAI
errAstbury, C; Christ, LA; Aughton, DJ; Cassidy, SB; Fujimoto, A; Pletcher, BA; Schafer, IA; Schwartz, S
err分享
err收藏
Detection of deletions in de novo balanced chromosome rearrangements: Further evidence for their role in phenotypic abnormalities从头平衡染色体重排中缺失的检测: 它们在表型异常中的作用的进一步证据
errGENETICS IN MEDICINE
IF6.2
err2004-03-01
err41
errOAAI
errAstbury, C; Christ, LA; Aughton, DJ; Cassidy, SB; Kumar, A; Eichler, EE; Schwartz, S
err分享
err收藏
Myeloid leukemia in Prader-Willi syndrome
errJOURNAL OF PEDIATRICS
IF3.5
err2003-02-01
err47
PREAI
errDavies, HD; Leusink, GL; McConnell, A; Deyell, M; Cassidy, SB; Rick, GH; Coppes, MJ
err分享
err收藏
The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria
errPEDIATRICS
IF6.4
err2001-11-01
err364
PREAI
errGunay-Aygun, M; Schwartz, S; Heeger, S; O'Riordan, MA; Cassidy, SB
err分享
err收藏
Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations
errHUMAN GENETICS
IF3.6
err2001-07-31
err41
PREAI
errRosenberg, MJ; Killoran, C; Dziadzio, L; Chang, S; Stone, DL; Meck, J; Aughton, D; Bird, LM; Bodurtha, J; Cassidy, SB; Graham, JM; Grix, A; Guttmacher, AE; Hudgins, L; Kozma, C; Michaelis, RC; Pauli, R; Peters, KF; Rosenbaum, KN; Tifft, CJ; Wargowski, D; Williams, MS; Biesecker, LG
err分享
err收藏
Genetics of childhood disorders: XII. Genomic imprinting: Breaking the rules
errJOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
IF9.5
err2000-03-01
err7
errOAAI
errEverman, DB; Cassidy, SB
err分享
err收藏
Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err1999-08-01
err211
errOAAI
errAmos-Landgraf, JM; Ji, YG; Gottlieb, W; Depinet, T; Wandstrat, AE; Cassidy, SB; Driscoll, DJ; Rogan, PK; Schwartz, S; Nicholls, RD
err分享
err收藏
The risk of testicular cancer in males with Prader-Willi syndrome (PWS) registered with the US PWS Association
errPEDIATRIC RESEARCH
IF3.1
err1999-04-01
err2
errOAAI
errCoppes, MJ; Rose, S; Cassidy, S; McConnell, A; Deyell, M; Davies, D
err分享
err收藏
Molecular mechanism of Angelman syndrome in two large families involves an imprinting mutation
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err1999-02-01
err73
errOAAI
errOhta, T; Buiting, K; Kokkonen, H; McCandless, S; Heeger, S; Leisti, H; Driscoll, DJ; Cassidy, SB; Horsthemke, B; Nicholls, RD
err分享
err收藏
Prader-Willi syndrome
errAMERICAN JOURNAL OF PSYCHIATRY
IF14.7
err1998-09-01
err39
PREAI
errMartin, A; State, M; Koenig, K; Schultz, R; Dykens, EM; Cassidy, SB; Leckman, JF
err分享
err收藏
Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome
errGENES CHROMOSOMES & CANCER
IF2.8
err1998-02-01
err52
PREAI
errTsuchiya, KD; Wiesner, G; Cassidy, SB; Limwongse, C; Boyle, JT; Schwartz, S
err分享
err收藏

研究方向

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L
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H 指数: 103 · 论文数: 775
M
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H 指数: 90 · 论文数: 261
H
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