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1

Identification of candidate genes for familial early-onset essential tremor

Liu, Xinmin, Hernandez, Nora, Kisselev, Sergey, Floratos, Aris, Sawle, Ashley, Ionita-Laza, Iuliana, Ottman, Ruth, Louis, Elan D, Clark, Lorraine N

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.12 MB

english, 2015

2

Co-localization between Sequence Constraint and Epigenomic Information Improves Interpretation of Whole-Genome Sequencing Data

Xu, Danqing, Wang, Chen, Kiryluk, Krzysztof, Buxbaum, Joseph D., Ionita-Laza, Iuliana

Journal:

The American Journal of Human Genetics

Year:

2020

File:

PDF, 1.53 MB

2020

3

Halorina cryptica nov. ichnogen., nov. ichnosp., mass-occurrence of Upper Triassic crustacean microcoprolites from neptunian dikes and sills cutting the Dachstein-type carbonate platform and their paleoenvironmental significance (Northern Apuseni Mountains, Romania)

LazÄr, Iuliana, Schlagintweit, Felix, GrÄdinaru, Eugen

Journal:

Year:

2020

File:

PDF, 3.45 MB

2020

4

Linkage disequilibrium mapping of the chromosome 6q21–22.31 bipolar I disorder susceptibility locus

Jinbo Fan, Iuliana Ionita-Laza, Matthew B. McQueen, Bernie Devlin, Shaun Purcell, Stephen V. Faraone, Michael H. Allen, Charles L. Bowden, Joseph R. Calabrese, Mark D. Fossey, Edward S. Friedman, Lasz

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2010

Language:

english

File:

PDF, 256 KB

english, 2010

5

On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test

Iuliana Ionita-Laza, George H. Perry, Benjamin A. Raby, Barbara Klanderman, Charles Lee, Nan M. Laird, Scott T. Weiss, Christoph Lange

Journal:

Genetic Epidemiology

Year:

2008

Language:

english

File:

PDF, 1.06 MB

english, 2008

6

Response to Macgregor

Iuliana Ionita-Laza, Matthew B. McQueen, Scott Weiss, Nan M. Laird, Christoph Lange

Journal:

The American Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 55 KB

english, 2008

7

Finding Disease Variants in Mendelian Disorders By Using Sequence Data: Methods and Applications

Iuliana Ionita-Laza, Vlad Makarov, Seungtai Yoon, Benjamin Raby, Joseph Buxbaum, Dan L. Nicolae, Xihong Lin

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 620 KB

english, 2011

8

Scan-Statistic Approach Identifies Clusters of Rare Disease Variants in LRP2, a Gene Linked and Associated with Autism Spectrum Disorders, in Three Datasets

Iuliana Ionita-Laza, Vlad Makarov, Joseph D. Buxbaum

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 598 KB

english, 2012

9

De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia

Xu, Bin, Ionita-Laza, Iuliana, Roos, J Louw, Boone, Braden, Woodrick, Scarlet, Sun, Yan, Levy, Shawn, Gogos, Joseph A, Karayiorgou, Maria

Journal:

Nature Genetics

Year:

2012

Language:

english

File:

PDF, 447 KB

english, 2012

10

Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis

Iuliana Ionita-Laza, Angela J. Rogers, Christoph Lange, Benjamin A. Raby, Charles Lee

Journal:

Year:

2009

Language:

english

File:

PDF, 340 KB

english, 2009

11

Genomewide Weighted Hypothesis Testing in Family-Based Association Studies, with an Application to a 100K Scan

Iuliana Ionita-Laza, Matthew B. McQueen, Nan M. Laird, Christoph Lange

Journal:

The American Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 231 KB

english, 2007

12

Identifying rare disease variants in the Genetic Analysis Workshop 17 simulated data: a comparison of several statistical approaches

Ruixue Fan, Chien-Hsun Huang, Shaw-Hwa Lo, Tian Zheng, Iuliana Ionita-Laza

Journal:

BMC Proceedings

Year:

2011

Language:

english

File:

PDF, 133 KB

english, 2011

13

Response to Ott and Hoh

Iuliana Ionita-Laza, Joseph D. Buxbaum

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 41 KB

english, 2012

14

Sequence Kernel Association Tests for the Combined Effect of Rare and Common Variants

Ionita-Laza, Iuliana, Lee, Seunggeun, Makarov, Vlad, Buxbaum, Joseph D., Lin, Xihong

Journal:

The American Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 430 KB

english, 2013

15

Statistical Challenges in Sequence-Based Association Studies with Population- and Family-Based Designs

Iuliana Ionita-Laza, Michael H. Cho, Nan M. Laird

Journal:

Statistics in Biosciences

Year:

2013

Language:

english

File:

PDF, 545 KB

english, 2013

16

Copy number variation genotyping using family information

Jen-hwa Chu, Angela Rogers, Iuliana Ionita-Laza, Katayoon Darvishi…

Journal:

BMC Bioinformatics

Year:

2013

Language:

english

File:

PDF, 3.05 MB

english, 2013

17

Family-based association tests for sequence data, and comparisons with population-based association tests

Ionita-Laza, Iuliana, Lee, Seunggeun, Makarov, Vladimir, Buxbaum, Joseph D, Lin, Xihong

Journal:

European Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 1.34 MB

english, 2013

18

Does rate of progression run in essential tremor families? Slower vs. faster progressors

Louis, Elan D., Hernandez, Nora, Ionita-Laza, Iuliana, Ottman, Ruth, Clark, Lorraine N.

Journal:

Parkinsonism & Related Disorders

Year:

2013

Language:

english

File:

PDF, 222 KB

english, 2013

19

Comparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data

Jing Huang,Yong Chen,Michael D Swartz,Iuliana Ionita-Laza

Journal:

BMC Proceedings

Year:

2014

Language:

english

File:

PDF, 1.08 MB

english, 2014

20

Genetic variants within the serotonin transporter associated with familial risk for major depression

Talati, Ardesheer, Guffanti, Guia, Odgerel, Zagaa, Ionita-Laza, Iuliana, Malm, Heli, Sourander, Andre, Brown, Alan S., Wickramaratne, Priya J., Gingrich, Jay A., Weissman, Myrna M.

Journal:

Psychiatry Research

Year:

2015

Language:

english

File:

PDF, 231 KB

english, 2015

21

On the Optimal Design of Genetic Variant Discovery Studies

Ionita-Laza, Iuliana, Laird, Nan M

Journal:

Statistical Applications in Genetics and Molecular Biology

Year:

2010

Language:

english

File:

PDF, 1.71 MB

english, 2010

22

Rare Variant Analysis for Family-Based Design

De, Gourab, Yip, Wai-Ki, Ionita-Laza, Iuliana, Laird, Nan, Xiong, Momiao

Journal:

Year:

2013

Language:

english

File:

PDF, 307 KB

english, 2013

23

Identification of Rare Causal Variants in Sequence-Based Studies: Methods and Applications to VPS13B, a Gene Involved in Cohen Syndrome and Autism

Ionita-Laza, Iuliana, Capanu, Marinela, De Rubeis, Silvia, McCallum, Kenneth, Buxbaum, Joseph D., Zeggini, Eleftheria

Journal:

Year:

2014

Language:

english

File:

PDF, 840 KB

english, 2014

24

A New Testing Strategy to Identify Rare Variants with Either Risk or Protective Effect on Disease

Ionita-Laza, Iuliana, Buxbaum, Joseph D., Laird, Nan M., Lange, Christoph, Leal, Suzanne M.

Journal:

Year:

2011

Language:

english

File:

PDF, 153 KB

english, 2011

25

Empirical Bayes scan statistics for detecting clusters of disease risk variants in genetic studies

McCallum, Kenneth J., Ionita-Laza, Iuliana

Journal:

Year:

2015

File:

PDF, 250 KB

2015

26

Empirical Bayes scan statistics for detecting clusters of disease risk variants in genetic studies

McCallum, Kenneth J., Ionita-Laza, Iuliana

Journal:

Year:

2015

Language:

english

File:

PDF, 250 KB

english, 2015

27

A spectral approach integrating functional genomic annotations for coding and noncoding variants

Ionita-Laza, Iuliana, McCallum, Kenneth, Xu, Bin, Buxbaum, Joseph D

Journal:

Nature Genetics

Year:

2016

Language:

english

File:

PDF, 1.21 MB

english, 2016

28

Quantile Regression in the Secondary Analysis of Case-Control Data

Wei, Ying, Song, Xiaoyu, Liu, Mengling, Ionita-Laza, Iuliana, Reibman, Joan

Journal:

Journal of the American Statistical Association

Year:

2015

Language:

english

File:

PDF, 127 KB

english, 2015

29

De Novo Synonymous Mutations in Regulatory Elements Contribute to the Genetic Etiology of Autism and Schizophrenia

Takata, Atsushi, Ionita-Laza, Iuliana, Gogos, Joseph A., Xu, Bin, Karayiorgou, Maria

Journal:

Year:

2016

Language:

english

File:

PDF, 1.19 MB

english, 2016

30

QRank: a novel quantile regression tool for eQTL discovery

Song, Xiaoyu, Li, Gen, Zhou, Zhenwei, Wang, Xianling, Ionita-Laza, Iuliana, Wei, Ying

Journal:

Year:

2017

Language:

english

File:

PDF, 1.23 MB

english, 2017

31

Joint study of genetic regulators for expression traits related to breast cancer

Tian Zheng,Shuang Wang,Lei Cong,Yuejing Ding,Iuliana Ionita-Laza…

Journal:

BMC Proceedings

Year:

2007

Language:

english

File:

PDF, 2.17 MB

english, 2007

32

Constructing gene association networks for rheumatoid arthritis using the backward genotype-trait association (BGTA) algorithm

Yuejing Ding,Lei Cong,Iuliana Ionita-Laza,Shaw-Hwa Lo,Tian Zheng

Journal:

BMC Proceedings

Year:

2007

Language:

english

File:

PDF, 1.67 MB

english, 2007

33

Unified Sequence-Based Association Tests Allowing for Multiple Functional Annotations and Meta-Analysis of Noncoding Variation in Metabochip Data

He, Zihuai, Xu, Bin, Lee, Seunggeun, Ionita-Laza, Iuliana

Journal:

The American Journal of Human Genetics

Year:

2017

Language:

english

File:

PDF, 1.14 MB

english, 2017

34

Rare-variant association tests in longitudinal studies, with an application to the Multi-Ethnic Study of Atherosclerosis (MESA)

He, Zihuai, Lee, Seunggeun, Zhang, Min, Smith, Jennifer A., Guo, Xiuqing, Palmas, Walter, Kardia, Sharon L.R., Ionita-Laza, Iuliana, Mukherjee, Bhramar

Journal:

Genetic Epidemiology

Year:

2017

Language:

english

File:

PDF, 269 KB

english, 2017

35

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

Sanna-Cherchi, Simone, Khan, Kamal, Westland, Rik, Krithivasan, Priya, Fievet, Lorraine, Rasouly, Hila Milo, Ionita-Laza, Iuliana, Capone, Valentina P., Fasel, David A., Kiryluk, Krzysztof, Kamalakara

Journal:

The American Journal of Human Genetics

Year:

2017

Language:

english

File:

PDF, 1.06 MB

english, 2017

36

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

Sanna-Cherchi, Simone, Khan, Kamal, Westland, Rik, Krithivasan, Priya, Fievet, Lorraine, Rasouly, Hila Milo, Ionita-Laza, Iuliana, Capone, Valentina P., Fasel, David A., Kiryluk, Krzysztof, Kamalakara

Journal:

The American Journal of Human Genetics

Year:

2017

Language:

english

File:

PDF, 53 KB

english, 2017

37

FUN-LDA: A Latent Dirichlet Allocation Model for Predicting Tissue-Specific Functional Effects of Noncoding Variation: Methods and Applications

Backenroth, Daniel, He, Zihuai, Kiryluk, Krzysztof, Boeva, Valentina, Pethukova, Lynn, Khurana, Ekta, Christiano, Angela, Buxbaum, Joseph D., Ionita-Laza, Iuliana

Journal:

The American Journal of Human Genetics

Year:

2018

Language:

english

File:

PDF, 1.72 MB

english, 2018

38

Essential Tremor in aCharcot-Marie-Tooth Type 2C Kindred Does Not Segregate with the TRPV4 R269H Mutation

Louis, Elan D., Hernandez, Nora, Ottman, Ruth, Ionita-Laza, Iuliana, Clark, Lorraine N.

Journal:

Case Reports in Neurology

Year:

2014

Language:

english

File:

PDF, 903 KB

english, 2014

39

Integrative analysis of functional genomic annotations and sequencing data to identify rare causal variants via hierarchical modeling

Capanu, Marinela, Ionita-Laza, Iuliana

Journal:

Frontiers in Genetics

Year:

2015

Language:

english

File:

PDF, 295 KB

english, 2015

40

A semi-supervised approach for predicting cell-type specific functional consequences of non-coding variation using MPRAs

He, Zihuai, Liu, Linxi, Wang, Kai, Ionita-Laza, Iuliana

Journal:

Nature Communications

Year:

2018

Language:

english

File:

PDF, 1.48 MB

english, 2018

41

A genome-wide scan statistic framework for whole-genome sequence data analysis

He, Zihuai, Xu, Bin, Buxbaum, Joseph, Ionita-Laza, Iuliana

Journal:

Nature Communications

Year:

2019

Language:

english

File:

PDF, 686 KB

english, 2019

42

Differences in plasma metabolites related to Alzheimer's disease, APOE Îµ4 status, and ethnicity

Vardarajan, Badri, Kalia, Vrinda, Manly, Jennifer, Brickman, Adam, ReyesâDumeyer, Dolly, Lantigua, Rafael, IonitaâLaza, Iuliana, Jones, Dean P., Miller, Gary W., Mayeux, Richard

Journal:

Alzheimer s & Dementia Translational Research & Clinical Interventions

Year:

2020

File:

PDF, 2.56 MB

2020

43

[American Thoracic Society American Thoracic Society 2010 International Conference, May 14-19, 2010 â¢ New Orleans - ()] B93. GENOME-WIDE APPROACHES FOR THE IDENTIFICATION OF ASTHMA GENES: NEW METHODS, NEW PHENOTYPES, NEW GENES - A Genome-wide Analysis Of The Role Of Copy Number Variants In Asthma

Rogers, Angela, Darvishi, Katayoon, Chu, Jen-Hwa, Ionita-Laza, Iuliana, Klanderman, Barbara J., Lee, Charles, Raby, Benjamin

Year:

2010

File:

PDF, 17 KB

2010

44

[American Thoracic Society American Thoracic Society 2011 International Conference, May 13-18, 2011 â¢ Denver Colorado - ()] D101. ASTHMA GENETICS - A Genome-Wide Screen Of Functional Dna Copy Number Variants Identifies Several Novel Asthma Genes

Rogers, Angela J., Chu, Jen-Hwa, Darvishi, Katayoon, Ionita-Laza, Iuliana, Klanderman, Barbara J., Lee, Charles, Raby, Benjamin A.

Year:

2011

File:

PDF, 17 KB

2011

45

[American Thoracic Society American Thoracic Society 2012 International Conference, May 18-23, 2012 â¢ San Francisco, California - ()] D31. ADVANCES IN ASTHMA GENETICS - A Genome-Wide Analysis Of The Role Of Copy Number Variants In Asthma

Rogers, Angela J., Darvishi, Katayoon, Chu, JenHwa, Ionita-Laza, Iuliana, Geigenmuller, Ute, Lee, Charles, Raby, Benjamin A.

Year:

2012

File:

PDF, 23 KB

2012

46

Cell Type-Specific Annotation and Fine Mapping of Variants Associated With Brain Disorders

Doostparast Torshizi, Abolfazl, Ionita-Laza, Iuliana, Wang, Kai

Journal:

Frontiers in Genetics

Year:

2020

File:

PDF, 2.81 MB

2020