Suzanne Leal : rechercher sur Z-Library

Campagne de collecte 15 septembre 2024 – 1 octobre 2024 C'est quoi, la collecte de fonds?

Le plus grand référentiel d'articles scientifiques au monde. 70,000,000+ d'articles gratuitement.

Campagne de collecte 15 septembre 2024 – 1 octobre 2024

Z-Library est une des plus grandes bibliothèques en ligne dans le monde, avec le stockage de plus de 17,000,000 livres et plus de 84,837,000 articles. Nous encourageons l'accès libre de chacun à la littérature. Aujourd'hui (15 septembre 2024) nous faisons un appel de fonds à tous ceux qui veulent contribuer encore plus au soutien et au développement de notre projet.

Les téléchargements SANS LIMITE sont aussi (au cours de 31 jours après la date de don) disponibles pour TOUS les utilisateurs qui soient en mesure de soutenir le projet pendant la période de collecte de fonds jusqu'au 1 octobre 2024.

C'est quoi, la collecte de fonds?En savoir plus

Livres
Articles (139)
Les plus populaires
Liste
- Liste
- Tableau

1

The genetics of colored sequence synesthesia: Evidence of linkage to chromosome 16q and genetic heterogeneity for the condition

Nelson, Stephanie, Avidan, Nili, Sarma, Anand, Tushe, Rejnal, Milewicz, Dianna, Lee, Kwanghyuk, Bray, Molly, Leal, Suzanne, Eagleman, David

Journal:

Bioentrepreneur

Année:

2009

Fichier:

PDF, 277 KB

2009

2

The genetics of colored sequence synesthesia: Suggestive evidence of linkage to 16q and genetic heterogeneity for the condition

Steffie N. Tomson, Nili Avidan, Kwanghyuk Lee, Anand K. Sarma, Rejnal Tushe, Dianna M. Milewicz, Molly Bray, Suzanne M. Leal, David M. Eagleman

Journal:

Behavioural Brain Research

Année:

2011

Langue:

english

Fichier:

PDF, 645 KB

english, 2011

3

Next generation analytic tools for large scale genetic epidemiology studies of complex diseases

Leah E. Mechanic, Huann-Sheng Chen, Christopher I. Amos, Nilanjan Chatterjee, Nancy J. Cox, Rao L. Divi, Ruzong Fan, Emily L. Harris, Kevin Jacobs, Peter Kraft, Suzanne M. Leal, Kimberly McAllister, J

Journal:

Genetic Epidemiology

Année:

2012

Langue:

english

Fichier:

PDF, 161 KB

english, 2012

4

A second generation human haplotype map of over 3.1 million SNPs

Frazer, Kelly A., Ballinger, Dennis G., Cox, David R., Hinds, David A., Stuve, Laura L., Gibbs, Richard A., Belmont, John W., Boudreau, Andrew, Hardenbol, Paul, Leal, Suzanne M.

Journal:

Année:

2007

Langue:

english

Fichier:

PDF, 1.01 MB

english, 2007

5

Variant Association Tools for Quality Control and Analysis of Large-Scale Sequence and Genotyping Array Data

Wang, Gao T., Peng, Bo, Leal, Suzanne M.

Journal:

The American Journal of Human Genetics

Année:

2014

Langue:

english

Fichier:

PDF, 2.51 MB

english, 2014

6

A Novel Adaptive Method for the Analysis of Next-Generation Sequencing Data to Detect Complex Trait Associations with Rare Variants Due to Gene Main Effects and Interactions

Liu, Dajiang J., Leal, Suzanne M., Gibson, Greg

Journal:

Année:

2010

Langue:

english

Fichier:

PDF, 1.03 MB

english, 2010

7

An entertainment-education colorectal cancer screening decision aid for African American patients: A randomized controlled trial

Hoffman, Aubri S., Lowenstein, Lisa M., Kamath, Geetanjali R., Housten, Ashley J., Leal, Viola B., Linder, Suzanne K., Jibaja-Weiss, Maria L., Raju, Gottumukkala S., Volk, Robert J.

Journal:

Année:

2017

Langue:

english

Fichier:

PDF, 275 KB

english, 2017

8

Randomized Phase II Trial of Cisplatin and Etoposide in Combination With Veliparib or Placebo for Extensive-Stage Small-Cell Lung Cancer: ECOG-ACRIN 2511 Study

Owonikoko, Taofeek K., Dahlberg, Suzanne E., Sica, Gabriel L., Wagner, Lynne I., Wade, James L., Srkalovic, Gordan, Lash, Bradley W., Leach, Joseph W., Leal, Ticiana B., Aggarwal, Charu, Ramalingam, S

Journal:

Journal of Clinical Oncology

Année:

2019

Langue:

english

Fichier:

PDF, 701 KB

english, 2019

9

The genetics of colored sequence synesthesia: Evidence of linkage to chromosome 16q and genetic heterogeneity for the condition

Nelson, Stephanie, Avidan, Nili, Sarma, Anand, Tushe, Rejnal, Milewicz, Dianna, Lee, Kwanghyuk, Bray, Molly, Leal, Suzanne, Eagleman, David

Journal:

Bioentrepreneur

Année:

2009

Langue:

english

Fichier:

PDF, 277 KB

english, 2009

10

Analysis of two-locus traits under heterogeneity for recessive versus dominant inheritance

Suzanne M. Leal, Jurg Ott

Journal:

Genetic Epidemiology

Année:

1997

Langue:

english

Fichier:

PDF, 24 KB

english, 1997

11

False positive rates in a genomic screen for complex quantitative traits

William K. Scott, Marcy C. Speer, Suzanne M. Leal, Linda M. Brzustowicz, Carol S. Haynes, Margaret A. Pericak-Vance

Journal:

Genetic Epidemiology

Année:

1997

Langue:

english

Fichier:

PDF, 32 KB

english, 1997

12

Phenotypes and genetic analysis of psychiatric and neuropsychiatric traits

Suzanne M. Leal

Journal:

American Journal of Medical Genetics Part A

Année:

2001

Langue:

english

Fichier:

PDF, 81 KB

english, 2001

13

Potentially functional polymorphism in the promoter region of prodynorphin gene may be associated with protection against cocaine dependence or abuse

Andrew C.H. Chen, K. Steven LaForge, Ann Ho, Pauline F. McHugh, Scott Kellogg, Kathy Bell, Rosemary P. Schluger, Suzanne M. Leal, Mary Jeanne Kreek

Journal:

American Journal of Medical Genetics Part A

Année:

2002

Langue:

english

Fichier:

PDF, 206 KB

english, 2002

14

Novel and previously reported single-nucleotide polymorphisms in the human 5-HT1B receptor gene: No association with cocaine or alcohol abuse or dependence

Tessa Cigler, K. Steven LaForge, Pauline F. McHugh, Sagar U. Kapadia, Suzanne M. Leal, Mary Jeanne Kreek

Journal:

American Journal of Medical Genetics Part A

Année:

2001

Langue:

english

Fichier:

PDF, 122 KB

english, 2001

15

Novel missense mutations and a 288-bp exonic insertion in PAX9 in families with autosomal dominant hypodontia

Parimal Das, Mehreen Hai, Claire Elcock, Suzanne M. Leal, Donald T. Brown, Alan H. Brook, Pragna I. Patel

Journal:

American Journal of Medical Genetics Part A

Année:

2003

Langue:

english

Fichier:

PDF, 272 KB

english, 2003

16

A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3

Muhammad Aslam, Muhammad Wajid, Maria H. Chahrour, Muhammad Ansar, Sayedul Haque, Thanh L. Pham, Regie P. Santos, Kai Yan, Wasim Ahmad, Suzanne M. Leal

Journal:

American Journal of Medical Genetics Part A

Année:

2005

Langue:

english

Fichier:

PDF, 78 KB

english, 2005

17

Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31

Asif Mir, Muhammad Ansar, Maria H. Chahrour, Thanh L. Pham, Muhammad Wajid, Sayedul Haque, Kai Yan, Wasim Ahmad, Suzanne M. Leal

Journal:

American Journal of Medical Genetics Part A

Année:

2005

Langue:

english

Fichier:

PDF, 68 KB

english, 2005

18

Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability

Kim L. McBride, Ricardo Pignatelli, Mark Lewin, Trang Ho, Susan Fernbach, Andres Menesses, Wilbur Lam, Suzanne M. Leal, Norman Kaplan, Paul Schliekelman, Jeffrey A. Towbin, John W. Belmont

Journal:

American Journal of Medical Genetics Part A

Année:

2005

Langue:

english

Fichier:

PDF, 89 KB

english, 2005

19

Terminal osseous dysplasia with pigmentary defects (TODPD): Follow-up of the first reported family, characterization of the radiological phenotype, and refinement of the linkage region

Nicola Brunetti-Pierri, Ralph Lachman, Kwanghyuk Lee, Suzanne M. Leal, Pasquale Piccolo, Ignatia B. Van Den Veyver, Carlos A. Bacino

Journal:

American Journal of Medical Genetics Part A

Année:

2010

Langue:

english

Fichier:

PDF, 233 KB

english, 2010

20

Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing loss

Kwanghyuk Lee, Muhammad Ansar, Paula B. Andrade, Bushra Khan, Regie Lyn P. Santos-Cortez, Wasim Ahmad, Suzanne M. Leal

Journal:

American Journal of Medical Genetics Part A

Année:

2012

Langue:

english

Fichier:

PDF, 293 KB

english, 2012

21

Mapping genes of complex psychiatric diseases in Daghestan genetic isolates

Kazima B. Bulayeva, Suzanne M. Leal, Tatiana A. Pavlova, Ruslan M. Kurbanov, Stephen J. Glatt, Oleg A. Bulayev, Ming T. Tsuang

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Année:

2005

Langue:

english

Fichier:

PDF, 145 KB

english, 2005

22

Chromosome 19p13 loci in Finnish migraine with aura families

Mari A. Kaunisto, Päivi J. Tikka, Mikko Kallela, Suzanne M. Leal, Jeanette C. Papp, Arja Korhonen, Eija Hämäläinen, Hanna Harno, Hannele Havanka, Markku Nissilä, Erkki Säkö, Matti Ilmavirta, Jaakko Ka

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Année:

2005

Langue:

english

Fichier:

PDF, 95 KB

english, 2005

23

Catechol-O-methyltransferase (COMT) gene variants: Possible association of the Val158Met variant with opiate addiction in hispanic women

Bronson E. Oosterhuis, K. Steven LaForge, Dmitri Proudnikov, Ann Ho, David A. Nielsen, Robert Gianotti, Sandra Barral, Derek Gordon, Suzanne M. Leal, Jurg Ott, Mary Jeanne Kreek

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 81 KB

english, 2008

24

Genetic maps of microsatellite and single-nucleotide polymorphism markers: Are the distances accurate?

Suzanne M. Leal

Journal:

Genetic Epidemiology

Année:

2003

Langue:

english

Fichier:

PDF, 107 KB

english, 2003

25

A bootstrap approach to estimating power for linkage heterogeneity

Dr. Suzanne M. Leal, Jurg Ott

Journal:

Genetic Epidemiology

Année:

1993

Langue:

english

Fichier:

PDF, 342 KB

english, 1993

26

Variability of genotype-specific penetrance probabilities in the calculation of risk support intervals

Suzanne M. Leal, Dr. Jurg Ott

Journal:

Genetic Epidemiology

Année:

1995

Langue:

english

Fichier:

PDF, 250 KB

english, 1995

27

Detection of genotyping errors and pseudo-SNPs via deviations from Hardy-Weinberg equilibrium

Suzanne M. Leal

Journal:

Genetic Epidemiology

Année:

2005

Langue:

english

Fichier:

PDF, 129 KB

english, 2005

28

Homozygosity Mapping of a Locus for a Novel Syndromic Ichthyosis to Chromosome 3q27-q28

Baala, Lekbir, Hadj-Rabia, Smail, Hamel-Teillac, Dominique, Hadchouel, Michelle, Prost, Catherine, Leal, Suzanne M., Jacquemin, Emmanuel, Sefiani, Abdelaziz, de Prost, Yves, Courtois, Gilles, Munnich,

Journal:

The Journal of Investigative Dermatology

Année:

2002

Langue:

english

Fichier:

PDF, 310 KB

english, 2002

29

Localization of a novel autosomal recessive nonsyndromic hearing impairment locusDFNB65to chromosome 20q13.2–q13.32

Aamira Tariq, Regie Lyn P. Santos, Mohammad Nasim Khan, Kwanghyuk Lee, Muhammad Jawad Hassan, Wasim Ahmad, Suzanne M. Leal

Journal:

Journal of Molecular Medicine

Année:

2006

Langue:

english

Fichier:

PDF, 198 KB

english, 2006

30

Novel sequence variants in theTMIEgene in families with autosomal recessive nonsyndromic hearing impairment

Regie Lyn P. Santos, Hatem El-Shanti, Shaheen Sikandar, Kwanghyuk Lee, Attya Bhatti, Kai Yan, Maria H. Chahrour, Nathan McArthur, Thanh L. Pham, Amjad Abdullah Mahasneh, Wasim Ahmad, Suzanne M. Leal

Journal:

Journal of Molecular Medicine

Année:

2006

Langue:

english

Fichier:

PDF, 131 KB

english, 2006

31

Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33–q27.3

Peter John, Ghazanfar Ali, Muhammad S. Chishti, Syed Muhammad S. Naqvi, Suzanne M. Leal, Wasim Ahmad

Journal:

Année:

2006

Langue:

english

Fichier:

PDF, 222 KB

english, 2006

32

DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2

Regie Lyn P. Santos, Muhammad Jawad Hassan, Shaheen Sikandar, Kwanghyuk Lee, Ghazanfar Ali, Protacio E. Martin, Michael Angelo L. Wambangco, Wasim Ahmad, Suzanne M. Leal

Journal:

Année:

2006

Langue:

english

Fichier:

PDF, 187 KB

english, 2006

33

DFNB89,a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2

Sulman Basit, Kwanghyuk Lee, Rabia Habib, Leon Chen, Umm-e-Kalsoom, Regie Lyn P. Santos-Cortez, Zahid Azeem, Paula Andrade, Muhammad Ansar, Wasim Ahmad, Suzanne M. Leal

Journal:

Année:

2011

Langue:

english

Fichier:

PDF, 404 KB

english, 2011

34

Splice-site mutations in theTRICgene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families

Muhammad S. Chishti, Attya Bhatti, Sana Tamim, Kwanghyuk Lee, Merry-Lynn McDonald, Suzanne M. Leal, Wasim Ahmad

Journal:

Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 373 KB

english, 2008

35

Mitochondrial DNA variant interactions modify breast cancer risk

Daniel Covarrubias, Ren-Kui Bai, Lee-Jun C. Wong, Suzanne M. Leal

Journal:

Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 184 KB

english, 2008

36

Complex phenotypes and complex genetics: An introduction to genetic studies of complex traits

John W. Belmont, Suzanne M. Leal

Journal:

Current Atherosclerosis Reports

Année:

2005

Langue:

english

Fichier:

PDF, 212 KB

english, 2005

37

A Recurrent Intragenic Deletion Mutation in DSG4 Gene in Three Pakistani Families with Autosomal Recessive Hypotrichosis

Rafiq, Muhammad Arshad, Ansar, Muhammad, Mahmood, Saqib, Haque, Sayedul, Faiyaz-ul-Haque, Muhammad, Leal, Suzanne M., Ahmad, Wasim

Journal:

The Journal of Investigative Dermatology

Année:

2004

Langue:

english

Fichier:

PDF, 57 KB

english, 2004

38

Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome)

McBride, Kim L, Zender, Gloria A, Fitzgerald-Butt, Sara M, Koehler, Daniel, Menesses-Diaz, Andres, Fernbach, Susan, Lee, Kwanghyuk, Towbin, Jeffrey A, Leal, Suzanne, Belmont, John W

Journal:

European Journal of Human Genetics

Année:

2009

Langue:

english

Fichier:

PDF, 345 KB

english, 2009

39

Missing heritability and strategies for finding the underlying causes of complex disease

Eichler, Evan E., Flint, Jonathan, Gibson, Greg, Kong, Augustine, Leal, Suzanne M., Moore, Jason H., Nadeau, Joseph H.

Journal:

Nature Reviews Genetics

Année:

2010

Langue:

english

Fichier:

PDF, 308 KB

english, 2010

40

A second Middle Eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9

Leal, Suzanne M, Apaydin, Fazil, Barnwell, Carol, Iber, Metin, Kandogan, Tolga, Pfister, Markus, Braendle, Uwe, Cura, Orhan, Schwalb, Marvin, Zenner, Hans-Peter

Journal:

European Journal of Human Genetics

Année:

1998

Langue:

english

Fichier:

PDF, 64 KB

english, 1998

41

A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1–14q24.3 in large consanguineous kindred from Pakistan

Ansar, Muhammad, Din, Mohammad Amin ud, Arshad, Muhammad, Sohail, Muhammad, Faiyaz-Ul-Haque, Mohammad, Haque, Sayedul, Ahmad, Wasim, Leal, Suzanne M

Journal:

European Journal of Human Genetics

Année:

2003

Langue:

english

Fichier:

PDF, 88 KB

english, 2003

42

DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22–q21.12

Wajid, Muhammad, Abbasi, Amir Ali, Ansar, Muhammad, Pham, Thanh L, Yan, Kai, Haque, Sayedul, Ahmad, Wasim, Leal, Suzanne M

Journal:

European Journal of Human Genetics

Année:

2003

Langue:

english

Fichier:

PDF, 70 KB

english, 2003

43

A locus for hereditary hypotrichosis localized to human chromosome 18q21.1

Rafique, Muhammad Arshad, Ansar, Muhammad, Jamal, Syed Muhammad, Malik, Sajid, Sohail, Muhammad, Faiyaz-Ul-Haque, Mohammad, Haque, Sayedul, Leal, Suzanne M, Ahmad, Wasim

Journal:

European Journal of Human Genetics

Année:

2003

Langue:

english

Fichier:

PDF, 110 KB

english, 2003

44

Multicenter Initiative Seeking Critical Genes in Respiratory Papillomatosis

Farrel J. Buchinsky, Craig S. Derkay, Suzanne M. Leal, Joseph Donfack, Garth D. Ehrlich, J Christopher Post

Journal:

The Laryngoscope

Année:

2004

Langue:

english

Fichier:

PDF, 1.09 MB

english, 2004

45

A Fast and Noise-Resilient Approach to Detect Rare-Variant Associations With Deep Sequencing Data for Complex Disorders

Yee Him Cheung, Gao Wang, Suzanne M. Leal, Shuang Wang

Journal:

Genetic Epidemiology

Année:

2012

Langue:

english

Fichier:

PDF, 928 KB

english, 2012

46

Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data

Bingshan Li, Suzanne M. Leal

Journal:

The American Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 227 KB

english, 2008

47

A Homozygous Mutation in ADAMTSL4 Causes Autosomal-Recessive Isolated Ectopia Lentis

Dina Ahram, T. Shawn Sato, Abdulghani Kohilan, Marwan Tayeh, Shan Chen, Suzanne Leal, Mahmoud Al-Salem, Hatem El-Shanti

Journal:

The American Journal of Human Genetics

Année:

2009

Langue:

english

Fichier:

PDF, 510 KB

english, 2009

48

Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74

Zubair M. Ahmed, Rizwan Yousaf, Byung Cheon Lee, Shaheen N. Khan, Sue Lee, Kwanghyuk Lee, Tayyab Husnain, Atteeq Ur Rehman, Sarah Bonneux, Muhammad Ansar, Wasim Ahmad, Suzanne M. Leal, Vadim N. Gladys

Journal:

The American Journal of Human Genetics

Année:

2011

Langue:

english

Fichier:

PDF, 1.52 MB

english, 2011

49

Replication Strategies for Rare Variant Complex Trait Association Studies via Next-Generation Sequencing

Dajiang J. Liu, Suzanne M. Leal

Journal:

The American Journal of Human Genetics

Année:

2010

Langue:

english

Fichier:

PDF, 167 KB

english, 2010

50

A distinct autosomal recessive ataxia maps to chromosome 12in an inbred family from Jordan

Hatem El-Shanti, Azhar Daoud, Ammar A. Sadoon, Suzanne M. Leal, Shan Chen, Kwanghyuk Lee, Ronald Spiegel

Journal:

Brain and Development

Année:

2006

Langue:

english

Fichier:

PDF, 216 KB

english, 2006