William Seltzer - Publications, H-index & Citations

William Seltzer

rutgers university new brunswick

32H指数

122论文数

4.9K被引数

收录论文 10

发表时间

Rare autosomal trisomies, revealed by maternal plasma DNA sequencing, suggest increased risk of feto-placental disease

SCIENCE TRANSLATIONAL MEDICINE

IF14.6

2017-08-30

121

OAAI

Pertile, Mark D.; Halks-Miller, Meredith; Flowers, Nicola; Barbacioru, Catalin; Kinnings, Sarah L.; Vavrek, Darcy; Seltzer, William K.; Bianchi, Diana W.

An empirical estimate of carrier frequencies for 400+causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals

GENETICS IN MEDICINE

IF6.2

2013-03-01

204

OAAI

Lazarin, Gabriel A.; Haque, Imran S.; Nazareth, Shivani; Iori, Kevin; Patterson, A. Scott; Jacobson, Jessica L.; Marshall, John R.; Seltzer, William K.; Patrizio, Pasquale; Evans, Eric A.; Srinivasan, Balaji S.

Biochemical markers in persons with preclinical familial Alzheimer disease

NEUROLOGY

IF8.5

2008-07-08

176

PREAI

Ringman, J. M.; Younkin, S. G.; Pratico, D.; Seltzer, W.; Cole, G. M.; Geschwind, D. H.; Rodriguez-Agudelo, Y.; Schaffer, B.; Fein, J.; Sokolow, S.; Rosario, E. R.; Gylys, K. H.; Varpetian, A.; Medina, L. D.; Cummings, J. L.

Late-onset hereditary axonal neuropathies

NEUROLOGY

IF8.5

2008-07-01

PREAI

Bennett, C. L.; Lawson, V. H.; Brickell, K. L.; Isaacs, K.; Seltzer, W.; Lipe, H. P.; Weiss, M. D.; Carter, G. T.; Flanigan, K. M.; Chance, P. F.; Bird, T. D.

Rare myelin protein zero sequence variant in late onset CMT1B

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2007-12-01

PREAI

Souayah, Nizar; Seltzer, W. K.; Brannagan, Thomas H.; Chin, Russell L.; Sander, Howard W.

Evaluating the clinical utility of a molecular genetic test for polycystic kidney disease

MOLECULAR GENETICS AND METABOLISM

IF3.5

2007-09-01

OAAI

Garcia-Gonzalez, Miguel A.; Jones, Jeffrey G.; Allen, Susan K.; Palatucci, Christopher M.; Batish, Sat D.; Seltzer, William K.; Lan, Zheng; Allen, Erica; Qian, Feng; Lens, Xose M.; Pei, York; Germino, Gregory G.; Watnick, Terry J.

A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort

GENETICS IN MEDICINE

IF6.2

2007-07-01

117

OAAI

Putcha, Girish V.; Bejjani, Bassem A.; Bleoo, Stacey; Booker, Jessica K.; Carey, John C.; Carson, Nancy; Das, Soma; Dempsey, Melissa A.; Gastier-Foster, Julie M.; Greinwald, John H., Jr.; Hoffmann, Marcy L.; Jeng, Linda Jo Bone; Kenna, Margaret A.; Khababa, Ishrag; Lilley, Margaret; Mao, Rong; Muralidharan, Kasinathan; Otani, Iris M.; Rehm, Heidi L.; Schaefer, Fred; Seltzer, William K.; Spector, Elaine B.; Springer, Michelle A.; Weck, Karen E.; Wenstrup, Richard J.; Withrow, Stacey; Wu, Bai-Lin; Zariwala, Maimoona A.; Schrijver, Iris

The spectrum of SCNIA-related infantile epileptic encephalopathies

BRAIN

IF11.7

2007-03-01

450

OAAI

Harkin, Louise A.; McMahon, Jacinta M.; Iona, Xenia; Dibbens, Leanne; Pelekanos, James T.; Zuberi, Sameer M.; Sadleir, Lynette G.; Andermann, Eva; Gill, Deepak; Farrell, Kevin; Connolly, Mary; Stanley, Thorsten; Harbord, Michael; Andermann, Frederick; Wang, Jing; Batish, Sat Dev; Jones, Jeffrey G.; Seltzer, William K.; Gardner, Alison; Sutherland, Grant; Berkovic, Samuel F.; Mulley, John C.; Scheffer, Ingrid E.

Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese

NEUROLOGY

IF8.5

2000-09-26

167

PREAI

Gwinn-Hardy, K; Chen, JY; Liu, HC; Liu, TY; Boss, M; Seltzer, W; Adam, A; Singleton, A; Koroshetz, W; Waters, C; Hardy, J; Farrer, M

Laboratory guidelines for Huntington disease genetic testing

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

1998-05-01

133

OAAI

Nance, MA; Seltzer, W; Ashizawa, T; Bennett, R; McIntosh, N; Myers, RH; Potter, T; Shea, DK

研究方向