Laura K Conlin: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

1

Effects on Blood Pressure of Reduced Dietary Sodium and the Dietary Approaches to Stop Hypertension (DASH) Diet

Sacks, Frank M., Svetkey, Laura P., Vollmer, William M., Appel, Lawrence J., Bray, George A., Harsha, David, Obarzanek, Eva, Conlin, Paul R., Miller, Edgar R., Simons-Morton, Denise G., Karanja, Njeri

Journal:

Boston Medical and Surgical Journal

Year:

2001

Language:

english

File:

PDF, 175 KB

english, 2001

2

Effect of the Dietary Approaches to Stop Hypertension Diet and Reduced Sodium Intake on Blood Pressure Control

Laura P Svetkey, Denise G Simons-Morton, Michael A Proschan, Frank M Sacks, Paul R Conlin, David Harsha, Thomas J Moore, DASH-Sodium Collaborative Research Group

Journal:

Journal of Clinical Hypertension

Year:

2004

Language:

english

File:

PDF, 317 KB

english, 2004

3

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

Hart, M. Ragan, Biesecker, Barbara B., Blout, Carrie L., Christensen, Kurt D., Amendola, Laura M., Bergstrom, Katie L., Biswas, Sawona, Bowling, Kevin M., Brothers, Kyle B., Conlin, Laura K., Cooper,

Journal:

Genetics in Medicine

Year:

2018

Language:

english

File:

PDF, 476 KB

english, 2018

4

Mosaicism and clinical genetics

Spinner, Nancy B., Conlin, Laura K.

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Year:

2014

Language:

english

File:

PDF, 2.26 MB

english, 2014

5

Clonal diversity analysis using SNP microarray: a new prognostic tool for chronic lymphocytic leukemia

Linsheng Zhang, Iya Znoyko, Luciano J. Costa, Laura K. Conlin, Robert D. Daber, Sally E. Self, Daynna J. Wolff

Journal:

Cancer Genetics

Year:

2011

Language:

english

File:

PDF, 1.49 MB

english, 2011

6

Bilateral Pheochromocytomas, Hemihyperplasia, and Subtle Somatic Mosaicism: The Importance of Detecting Low-Level Uniparental Disomy

Kalish, Jennifer M., Conlin, Laura K., Mostoufi-Moab, Sogol, Wilkens, Alisha B., Mulchandani, Surabhi, Zelley, Kristin, Kowalski, Megan, Bhatti, Tricia R., Russo, Pierre, Mattei, Peter, Mackenzie, Wil

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 9.53 MB

english, 2013

7

Update on “Two Siblings With Alternate Unbalanced Recombinants Derived From a Large Cryptic Maternal Pericentric Inversion of Chromosome 20”

Cheryl DeScipio, Jennifer D. Morrissette, Laura K. Conlin, Dinah Clark, Maninder Kaur, James Coplan, Harold Riethman, Nancy B. Spinner, Ian D. Krantz

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 45 KB

english, 2010

8

Mutations in the ABCC6 Gene as a Cause of Generalized Arterial Calcification of Infancy: Genotypic Overlap with Pseudoxanthoma Elasticum

Li, Qiaoli, Brodsky, Jill L, Conlin, Laura K, Pawel, Bruce, Glatz, Andrew C, Gafni, Rachel I, Schurgers, Leon, Uitto, Jouni, Hakonarson, Hakon, Deardorff, Matthew A, Levine, Michael A

Journal:

The Journal of Investigative Dermatology

Year:

2014

Language:

english

File:

PDF, 1.58 MB

english, 2014

9

Detection of mutually exclusive mosaicism in a girl with genotype-phenotype discrepancies

Luo, Minjie, Mulchandani, Surabhi, Dubbs, Holly A., Swarr, Daniel, Pyle, Louise, Zackai, Elaine H., Spinner, Nancy B., Conlin, Laura K.

Journal:

American Journal of Medical Genetics Part A

Year:

2015

Language:

english

File:

PDF, 729 KB

english, 2015

10

A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories

O’Daniel, Julianne M., McLaughlin, Heather M., Amendola, Laura M., Bale, Sherri J., Berg, Jonathan S., Bick, David, Bowling, Kevin M., Chao, Elizabeth C., Chung, Wendy K., Conlin, Laura K., Cooper, Gr

Journal:

Genetics in Medicine

Year:

2016

Language:

english

File:

PDF, 638 KB

english, 2016

11

Utility of SNP arrays in detecting, quantifying, and determining meiotic origin of tetrasomy 12p in blood from individuals with Pallister-Killian syndrome

Conlin, Laura K., Kaur, Maninder, Izumi, Kosuke, Campbell, Lindsey, Wilkens, Alisha, Clark, Dinah, Deardorff, Matthew A., Zackai, Elaine H., Pallister, Phillip, Hakonarson, Hakon, Spinner, Nancy B., K

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 2.34 MB

english, 2012

12

Copy Number Detection in Exome Sequencing Compared to Chromosomal Microarray in a Clinical Setting

Rajagopalan, Ramakrishnan, Devkota, Batsal, Jayaraman, Vijayakumar, Biswas, Sawona, Spinner, Nancy B., Krantz, Ian D., Conlin, Laura K.

Journal:

Cancer Genetics

Year:

2016

Language:

english

File:

PDF, 48 KB

english, 2016

13

Sodium and blood pressure: no data dredging, please!

Frank M Sacks, Lawrence J Appel, George A Bray, Paul R Conlin, Thomas J Moore, Laura P Svetkey, William M Vollmer

Journal:

American Journal of Hypertension

Year:

2003

Language:

english

File:

PDF, 82 KB

english, 2003

14

Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion

Guilherme, Roberta Santos, Soares, Karina Cunha, Simioni, Milena, Vieira, Tarsis Paiva, Gil-da-Silva-Lopes, Vera Lúcia, Kim, Chong Ae, Brunoni, Décio, Spinner, Nancy Bettina, Conlin, Laura Kathleen, C

Journal:

American Journal of Medical Genetics Part A

Year:

2014

Language:

english

File:

PDF, 163 KB

english, 2014

15

CMIP haploinsufficiency in two patients with autism spectrum disorder and co-occurring gastrointestinal issues

Luo, Minjie, Fan, Jinbo, Wenger, Tara L., Harr, Margaret H., Racobaldo, Melissa, Mulchandani, Surabhi, Dubbs, Holly, Zackai, Elaine H., Spinner, Nancy B., Conlin, Laura K.

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 785 KB

english, 2017

16

28. Dosage sensitivity curation of recurrent copy number variant regions

Andersen, Erica, Burnside, Rachel, Coe, Bradley, Conlin, Laura, Herriges, John, Higginbotham, Ted, Hilton, Benjamin, Jobanputra, Vaidehi, Kearney, Hutton, Ouyang, Karen, Paulraj, Prabakaran, Riggs, Er

Journal:

Cancer Genetics

Year:

2018

Language:

english

File:

PDF, 56 KB

english, 2018

17

Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

Waggoner, Darrel, Wain, Karen E., Dubuc, Adrian M., Conlin, Laura, Hickey, Scott E., Lamb, Allen N., Martin, Christa Lese, Morton, Cynthia C., Rasmussen, Kristen, Schuette, Jane L., Schwartz, Stuart,

Journal:

Genetics in Medicine

Year:

2018

Language:

english

File:

PDF, 280 KB

english, 2018

18

Two siblings with alternate unbalanced recombinants derived from a large cryptic maternal pericentric inversion of chromosome 20

Cheryl DeScipio, Jennifer D. Morrissette, Laura K. Conlin, Dinah Clark, Maninder Kaur, James Coplan, Harold Riethman, Nancy B. Spinner, Ian D. Krantz

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 233 KB

english, 2010

19

Diagnostic Implications of Excessive Homozygosity Detected by SNP-Based Microarrays: Consanguinity, Uniparental Disomy, and Recessive Single-Gene Mutations

Kearney, Hutton M., Kearney, Joseph B., Conlin, Laura K.

Journal:

Clinics in Laboratory Medicine

Year:

2011

Language:

english

File:

PDF, 2.78 MB

english, 2011

20

Natural variation in human gene expression assessed in lymphoblastoid cells

Cheung, Vivian G., Conlin, Laura K., Weber, Teresa M., Arcaro, Melissa, Jen, Kuang-Yu, Morley, Michael, Spielman, Richard S.

Journal:

Nature Genetics

Year:

2003

Language:

english

File:

PDF, 598 KB

english, 2003

21

Duplication 12p and Pallister-Killian syndrome: A case report and review of the literature toward defining a Pallister-Killian syndrome minimal critical region

Izumi, Kosuke, Conlin, Laura K., Berrodin, Donna, Fincher, Christopher, Wilkens, Alisha, Haldeman-Englert, Chad, Saitta, Sulagna C., Zackai, Elaine H., Spinner, Nancy B., Krantz, Ian D.

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 727 KB

english, 2012

22

PECONPI: A novel software for uncovering pathogenic copy number variations in non-syndromic sensorineural hearing loss and other genetically heterogeneous disorders

Tsai, Ellen A., Berman, Micah A., Conlin, Laura K., Rehm, Heidi L., Francey, Lauren J., Deardorff, Matthew A., Holst, Jenelle, Kaur, Maninder, Gallant, Emily, Clark, Dinah M., Glessner, Joseph T., Jen

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 1.81 MB

english, 2013

23

Persistent Mosaicism for 12p Duplication/Triplication Chromosome Structural Abnormality in Peripheral Blood

Shackelford, Amy L., Conlin, Laura K., Hummel, Marybeth, Spinner, Nancy B., Wenger, Sharon L.

Journal:

Case Reports in Genetics

Year:

2013

Language:

english

File:

PDF, 950 KB

english, 2013

24

Investigating Structural Variation Using Optical Genome Mapping Technology

Rajagopalan, Ramakrishnan, McEldrew, Deborah, Vaidiswaran, Priya, Zaykaner, Michael, Jayaraman, Vijayakumar, McCaffrey, Jennifer, Sibert, Justin, Xiao, Ming, Conlin, Laura

Journal:

Cancer Genetics

Year:

2017

Language:

english

File:

PDF, 57 KB

english, 2017

25

Significant liver disease in a patient with Y116H mutation in the MVK gene

Melissa Leyva-Vega, Pamela F. Weiss, Jaya Ganesh, Laura Conlin, Nancy B. Spinner, Randolph P. Matthews

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 251 KB

english, 2011

26

Osteomas of the Skin Revisited

Conlin, Phillip A., Jimenez-Quintero, Laura P., Rapini, Ronald P.

Journal:

American Journal of Dermatopathology

Year:

2002

Language:

english

File:

PDF, 575 KB

english, 2002

27

Assessing Copy Number Variants Involving ACMGG Secondary Finding Genes Identified by Routine Chromosomal SNP Array in a Clinical Pediatric Population

Fan, Jinbo, Mulchandani, Surabhi, Dulik, Matthew, Chen, Jinyun, Gleason, Adam, Jayaraman, Pushkala, Sarmady, Mahdi, Zackai, Elaine, Luo, Minjie, Spinner, Nancy, Conlin, Laura

Journal:

Cancer Genetics

Year:

2016

Language:

english

File:

PDF, 37 KB

english, 2016

28

Mosaic ratio quantification of isochromosome 12p in Pallister-Killian syndrome using droplet digital PCR

Fujiki, Katsunori, Shirahige, Katsuhiko, Kaur, Maninder, Deardorff, Matthew A., Conlin, Laura K., Krantz, Ian D., Izumi, Kosuke

Journal:

Molecular Genetics & Genomic Medicine

Year:

2016

Language:

english

File:

PDF, 675 KB

english, 2016

29

Further evidence for the possible role of MEIS2 in the development of cleft palate and cardiac septum

Moira A. Crowley, Laura K. Conlin, Elaine H. Zackai, Matthew A. Deardorff, Brian D. Thiel, Nancy B. Spinner

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 179 KB

english, 2010

30

Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease

Matthew G. Sampson, Curtis R. Coughlin II, Paige Kaplan, Laura K. Conlin, Kevin E.C. Meyers, Elaine H. Zackai, Nancy B. Spinner, Lawrence Copelovitch

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 144 KB

english, 2010

31

Large genomic deletions: A novel cause of Ullrich congenital muscular dystrophy

A. Reghan Foley, Ying Hu, Yaqun Zou, Michele Yang, Līvija Medne, Meganne Leach, Laura K. Conlin, Nancy Spinner, Tamim H. Shaikh, Marni Falk, Ann M. Neumeyer, Laurie Bliss, Brian S. Tseng, Thomas L. Wi

Journal:

Annals of Neurology

Year:

2011

Language:

english

File:

PDF, 1.02 MB

english, 2011

32

Water structure in vitro and within Saccharomyces cerevisiae yeast cells under conditions of heat shock

Jennifer L. Dashnau, Laura K. Conlin, Hillary C.M. Nelson, Jane M. Vanderkooi

Journal:

Biochimica et Biophysica Acta (BBA) - General Subjects

Year:

2008

Language:

english

File:

PDF, 586 KB

english, 2008

33

Clinical features of three girls with mosaic genome-wide paternal uniparental isodisomy

Kalish, Jennifer M., Conlin, Laura K., Bhatti, Tricia R., Dubbs, Holly A., Harris, Mary Catherine, Izumi, Kosuke, Mostoufi-Moab, Sogol, Mulchandani, Surabhi, Saitta, Sulagna, States, Lisa J., Swarr, D

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 1.34 MB

english, 2013

34

DOCK3 -related neurodevelopmental syndrome: Biallelic intragenic deletion of DOCK3 in a boy with developmental delay and hypotonia

Iwata-Otsubo, Aiko, Ritter, Alyssa L., Weckselbatt, Brooke, Ryan, Nicole R., Burgess, David, Conlin, Laura K., Izumi, Kosuke

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 691 KB

english, 2017

35

Mosaic trisomy 17: Variable clinical and cytogenetic presentation

Robert Daber, Kimberly A. Chapman, Eduardo Ruchelli, Stefanie Kasperski, Surabhi Mulchandani, Brian D. Thiel, Hakon Hakonarson, Elaine H. Zackai, Laura K. Conlin, Nancy B. Spinner

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 618 KB

english, 2011

36

EGFR mutations cause a lethal syndrome of epithelial dysfunction with progeroid features

Ganetzky, Rebecca, Finn, Erin, Bagchi, Atrish, Zollo, Ornella, Conlin, Laura, Deardorff, Matthew, Harr, Margaret, Simpson, Michael A., McGrath, John A., Zackai, Elaine, Lemmon, Mark A., Sondheimer, Ne

Journal:

Molecular Genetics & Genomic Medicine

Year:

2015

Language:

english

File:

PDF, 994 KB

english, 2015

37

Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith–Wiedemann syndrome

Kalish, Jennifer M, Boodhansingh, Kara E, Bhatti, Tricia R, Ganguly, Arupa, Conlin, Laura K, Becker, Susan A, Givler, Stephanie, Mighion, Lindsey, Palladino, Andrew A, Adzick, N Scott, De León, Diva D

Journal:

Journal of Medical Genetics

Year:

2016

Language:

english

File:

PDF, 1.03 MB

english, 2016

38

1. Detection of mosaicism and chimerism using SNP arrays in pediatric clinical testing: 10 year experience

Conlin, Laura K., Weckselblatt, Brooke, Fan, Jinbo, Zackai, Elaine, Dulik, Matthew C., Spinner, Nancy B., Luo, Minjie

Journal:

Cancer Genetics

Year:

2018

Language:

english

File:

PDF, 45 KB

english, 2018

39

34. Genome-wide mosaicism, chimerism, and contamination: Recognizing and interpreting genotyping patterns from SNP arrays

Conlin, Laura K., Luo, Minjie, Weckselblatt, Brooke, Rafferty, Kelly A., Kalish, Jennifer, Zackai, Elaine H., Dulik, Matthew A., Spinner, Nancy B.

Journal:

Cancer Genetics

Year:

2018

Language:

english

File:

PDF, 48 KB

english, 2018

40

Evolution of histomorphologic, cytogenetic, and genetic abnormalities in an untreated patient with MIRAGE syndrome

Rentas, Stefan, Pillai, Vinodh, Wertheim, Gerald B., Akgumus, Gozde T., Nichols, Kim E., Deardorff, Matthew A., Conlin, Laura K., Li, Marilyn M., Olson, Timothy S., Luo, Minjie

Journal:

Cancer Genetics

Year:

2020

File:

PDF, 2.90 MB

2020

41

The Effects of Dietary Patterns on Urinary Albumin Excretion: Results of the Dietary Approaches to Stop Hypertension (DASH) Trial

David R. Jacobs Jr, Myron D. Gross, Lyn Steffen, Michael W. Steffes, Xinhua Yu, Laura P. Svetkey, Lawrence J. Appel, William M. Vollmer, George A. Bray, Thomas Moore, Paul R. Conlin, Frank Sacks

Journal:

American Journal of Kidney Diseases

Year:

2009

Language:

english

File:

PDF, 278 KB

english, 2009

42

The effects of sodium reduction and the DASH diet on ambulatory blood pressure (ABP) in African-Americans and non-African-Americans: results from the DASH-sodium feeding study

Lawrence J. Appel, Mikel Aickin, Paul R. Conlin, David W. Harsha, Gayle T. Meltesen, Thomas J. Moore, Frank M. Sacks, Laura P. Svetkey

Journal:

American Journal of Hypertension

Year:

2001

Language:

english

File:

PDF, 33 KB

english, 2001

43

[AIP 2007 PHYSICS EDUCATION RESEARCH CONFERENCE - Greensboro (NC) (1–2 August 2007)] AIP Conference Proceedings - The Dynamics of Students' Behaviors and Reasoning during Collaborative Physics Tutorial Sessions

Conlin, Luke D., Gupta, Ayush, Scherr, Rachel E., Hammer, David, Hsu, Leon, Henderson, Charles, McCullough, Laura

Year:

2007

Language:

english

File:

PDF, 291 KB

english, 2007

44

The Recurrent t(11;22)(q23;q11.2) Can Occur as a Post-Zygotic Event

Correll-Tash, Sarah, Conlin, Laura, Mininger, Beth A., Lilley, Brenna, Mennuti, Michael T., Emanuel, Beverly S.

Journal:

Cytogenetic and Genome Research

Year:

2018

Language:

english

File:

PDF, 501 KB

english, 2018

45

Protein‐elongating mutations in MYH11 are implicated in a dominantly‐inherited smooth muscle dysmotility syndrome with severe esophageal, gastric, and intestinal disease

Gilbert, Melissa A., Schultz‐Rogers, Laura, Rajagopalan, Ramakrishnan, Grochowski, Christopher M., Wilkins, Benjamin J., Biswas, Sawona, Conlin, Laura K., Fiorino, Kristin N., Dhamija, Radhika, Pack,

Journal:

Year:

2020

Language:

english

File:

PDF, 982 KB

english, 2020

46

Cytogenetic and molecular evaluation and 20-year follow-up of a patient with ring chromosome 14

Roberta Santos Guilherme, Vera de Freitas Ayres Meloni, Claudete Palmer Sodré, Denise Maria Christofolini, Renata Pellegrino, Claudia Berlim de Mello, Laura Kathleen Conlin, Anne Lawlor Hutchinson, Na

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 152 KB

english, 2010

47

Fine-mapping subtelomeric deletions and duplications by comparative genomic hybridization in 42 individuals

Cheryl DeScipio, Nancy B. Spinner, Maninder Kaur, Dinah Yaeger, Laura K. Conlin, Anthony Ambrosini, Sufen Hu, Simei Shan, Ian D. Krantz, Harold Riethman

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 175 KB

english, 2008

48

Circadian Hematologic Time Structure in the Elderly

Swoyer, Jacqueline, Irvine, Patrick, Sackett-Lundeen, Linda, Conlin, Laura, Lakatua, David, Haus, Erhard

Journal:

Chronobiology International

Year:

1989

Language:

english

File:

PDF, 481 KB

english, 1989

49

Subtelomeric deletion of chromosome 10p15.3: Clinical findings and molecular cytogenetic characterization

Cheryl DeScipio, Laura Conlin, Jill Rosenfeld, James Tepperberg, Romela Pasion, Ankita Patel, Marie T. McDonald, Swaroop Aradhya, Darlene Ho, Jennifer Goldstein, Marianne McGuire, Surabhi Mulchandani,

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 286 KB

english, 2012

50

SHIP-Deficient Mice Develop Spontaneous Intestinal Inflammation and Arginase-Dependent Fibrosis

Keith W. McLarren, Alexandra E. Cole, Shelley B. Weisser, Nicole S. Voglmaier, Victoria S. Conlin, Kevan Jacobson, Oana Popescu, Jean-Luc Boucher, Laura M. Sly

Journal:

The American Journal of Pathology

Year:

2011

Language:

english

File:

PDF, 2.85 MB

english, 2011

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@1delivery.pm

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски