Christa Lese Martin

Получаване на мой собствен потребителски профил

Позовавания

	Всички	От 2020
Позовавания	42275	18560
h-индекс	79	54
i10-индекс	158	131

3900

1950

975

2925

2004200520062007200820092010201120122013201420152016201720182019202020212022202320242025115 132 160 336 702 791 916 1105 1252 1648 2209 2471 2574 2666 2944 3013 3272 3778 3857 3497 3502 625

Публичен достъп

Преглед на всички

112 статии

2 статии

налични

неналични

Въз основа на изисквания при финансирането

Съавтори

David H. Ledbetter, PhD, FACMGProfessor, Institute for Pediatric Rare Diseases, Florida State University College of MedicineПотвърден имейл адрес: med.fsu.edu
Dan GeschwindDistinguished Professor of Neurology, Psychiatry and Human Genetics, UCLAПотвърден имейл адрес: mednet.ucla.edu
Marc S. WilliamsProfessor and Director Emeritus, Genomic Medicine Institute, GeisingerПотвърден имейл адрес: geisinger.edu
Andres Moreno-De-Luca, MD, MBA, D...Diagnostic Neuroradiologist, Mayfair DiagnosticsПотвърден имейл адрес: radiology.ca
Stephan J. SandersProfessor, Oxford and UCSFПотвърден имейл адрес: ucsf.edu
Daniel Moreno De Luca, MD MScCASA Research Chair, Associate Professor, University of AlbertaПотвърден имейл адрес: ualberta.ca
Matthew StateucsfПотвърден имейл адрес: ucsf.edu
William Andrew FaucettRetired, IRB Co-Chair, Geisinger Health SystemПотвърден имейл адрес: geisinger.edu
Evan EichlerProfessor of Genome Sciences, University of WashingtonПотвърден имейл адрес: gs.washington.edu
Christopher A WalshBoston Children's HospitalПотвърден имейл адрес: childrens.harvard.edu
James S SutcliffeAssociate Professor, Vanderbilt UniversityПотвърден имейл адрес: vanderbilt.edu
Carlos CARDOSO, PhDINSERM - INMED, Marseille, FranceПотвърден имейл адрес: inserm.fr
Katie RuddMedical Director, ARUP LaboratoriesПотвърден имейл адрес: aruplab.com
Scherer, Stephen W.The Hospital for Sick Children, Genetics and Genome Biology Program, University of TorontoПотвърден имейл адрес: sickkids.ca
Brett Abrahams, PhDAlbert Einstein College of MedicineПотвърден имейл адрес: einstein.yu.edu
Stan NelsonProfessor of Human Genetics, UCLAПотвърден имейл адрес: ucla.edu
Naomichi MatsumotoYokohama City UniversityПотвърден имейл адрес: yokohama-cu.ac.jp
Vanessa L. HornerUniversity of Wisconsin-MadisonПотвърден имейл адрес: slh.wisc.edu
Camille RaginProfessor, Fox Chase Cancer CenterПотвърден имейл адрес: fccc.edu
Mario CáceresICREA Research Professor, Hospital del Mar Research InstituteПотвърден имейл адрес: icrea.cat

Следене

Christa Lese Martin

Chief Scientific Officer, Geisinger; Professor and Director, Autism & Developmental

Потвърден имейл адрес: geisinger.edu - Начална страница

Precision Health Human Genomics Cytogenomics Developmental Medicine Autism


Заглавие Сортиране по цитати Сортиране по година Сортиране по заглавие	Позовавания Позовавания	Година
Strong association of de novo copy number mutations with autism J Sebat, B Lakshmi, D Malhotra, J Troge, C Lese-Martin, T Walsh, ... Science 316 (5823), 445-449, 2007	3532	2007
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies DT Miller, MP Adam, S Aradhya, LG Biesecker, AR Brothman, NP Carter, ... The American Journal of Human Genetics 86 (5), 749-764, 2010	3269	2010
CORRIGENDUM: ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing RC Green, JS Berg, WW Grody, SS Kalia, BR Korf, CL Martin, AL McGuire, ... Genetics in Medicine 19 (5), 606, 2017	2846*	2017
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing RC Green, JS Berg, WW Grody, SS Kalia, BR Korf, CL Martin, AL McGuire, ... Genetics in Medicine 15 (7), 565-574, 2013	2828	2013
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ... Nature genetics 45 (9), 984, 2013	2422	2013
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2. 0): a policy statement of the American College of Medical … SS Kalia, K Adelman, SJ Bale, WK Chung, C Eng, JP Evans, GE Herman, ... Genetics in Medicine 19 (4), 484-485, 2017	1782*	2017
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2. 0): a policy statement of the American College of Medical … SS Kalia, K Adelman, SJ Bale, WK Chung, C Eng, JP Evans, GE Herman, ... Genetics in Medicine 19 (2), 249, 2017	1778	2017
Mapping autism risk loci using genetic linkage and chromosomal rearrangements P Szatmari, AD Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ... Nature genetics 39 (3), 319-328, 2007	1644*	2007
Chromosomal microarray versus karyotyping for prenatal diagnosis RJ Wapner, CL Martin, B Levy, BC Ballif, CM Eng, JM Zachary, M Savage, ... New England Journal of Medicine 367 (23), 2175-2184, 2012	1627	2012
Chromosomal microarray versus karyotyping for prenatal diagnosis RJ Wapner, CL Martin, B Levy, BC Ballif, CM Eng, JM Zachary, M Savage, ... New England Journal of Medicine 367 (23), 2175-2184, 2012	1627	2012
Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci SJ Sanders, X He, AJ Willsey, AG Ercan-Sencicek, KE Samocha, ... Neuron 87 (6), 1215-1233, 2015	1583	2015
Multiple recurrent de novo copy number variations (CNVs), including duplications of the 7q11. 23 Williams-Beuren syndrome region, are strongly associated with autism SJ Sanders, AG Ercan-Sencicek, V Hus, R Luo, MT Murtha, ... Neuron 70 (5), 863, 2011	1571*	2011
ClinGen—The Clinical Genome Resource HL Rehm, JS Berg, LD Brooks, CD Bustamante, JP Evans, MJ Landrum, ... New England Journal of Medicine, 2015	1355	2015
Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics … ER Riggs, EF Andersen, AM Cherry, S Kantarci, H Kearney, A Patel, ... Genetics in Medicine 22 (2), 245-257, 2020	1335	2020
Linkage, Association, and Gene-Expression Analyses Identify< i> CNTNAP2</i> as an Autism-Susceptibility Gene M Alarcón, BS Abrahams, JL Stone, JA Duvall, JV Perederiy, JM Bomar, ... The American Journal of Human Genetics 82 (1), 150-159, 2008	1046	2008
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data S Köhler, SC Doelken, CJ Mungall, S Bauer, HV Firth, I Bailleul-Forestier, ... Nucleic acids research 42 (D1), D966-D974, 2014	948	2014
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways C O'Dushlaine, L Rossin, PH Lee, L Duncan, NN Parikshak, S Newhouse, ... Nature neuroscience 18 (2), 199, 2015	626	2015
Meta-analysis and multidisciplinary consensus statement: Exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders S Srivastava, JA Love-Nichols, KA Dies, DH Ledbetter, CL Martin, ... Genetics in Medicine, 1, 2019	577	2019
Evaluating the clinical validity of gene-disease associations: an evidence-based framework developed by the clinical genome resource NT Strande, ER Riggs, AH Buchanan, O Ceyhan-Birsoy, M DiStefano, ... The American Journal of Human Genetics 100 (6), 895-906, 2017	535	2017
Evaluating the clinical validity of gene-disease associations: an evidence-based framework developed by the Clinical Genome Resource NT Strande, ER Riggs, AH Buchanan, O Ceyhan-Birsoy, M DiStefano, ... The American Journal of Human Genetics 100 (6), 895-906, 2017	535	2017

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