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Ankita Patel

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

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Oligonucleotide Array Sequence Analysis

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Nucleic Acid Hybridization

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Physiology

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Infant

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TOP 3
Brunetti-Perri Nicola; Patel Ankita; Brown Chester W; Rauch Ronald A; Heptulla Rubina A
De novo terminal 22q12.3q13.3 duplication with pituitary hypoplasia.
Wang Xiaoling; Sutton V Reid; Eble Tanya N; Lewis Richard Alan; Gunaratne Preethi; Patel Ankita; Van den Veyver Ignatia B
A genome-wide screen for copy number alterations in Aicardi syndrome.
El-Hattab Ayman W; Smolarek Teresa A; Walker Martha E; Schorry Elizabeth K; Immken LaDonna L; Patel Gayle; Abbott Mary-Alice; Lanpher Brendan C; Ou Zhishuo; Kang Sung-Hae L; Patel Ankita; Scaglia Fernando; Lupski James R; Cheung Sau Wai; Stankiewicz Pawel
Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping.

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All Publications

2009: Brunetti-Perri Nicola; Patel Ankita; Brown Chester W; Rauch Ronald A; Heptulla Rubina A
De novo terminal 22q12.3q13.3 duplication with pituitary hypoplasia.
American journal of medical genetics. Part A 2009;149A(11):2554-6.
2009: Wang Xiaoling; Sutton V Reid; Eble Tanya N; Lewis Richard Alan; Gunaratne Preethi; Patel Ankita; Van den Veyver Ignatia B
A genome-wide screen for copy number alterations in Aicardi syndrome.
American journal of medical genetics. Part A 2009;149A(10):2113-21.
2009: El-Hattab Ayman W; Smolarek Teresa A; Walker Martha E; Schorry Elizabeth K; Immken LaDonna L; Patel Gayle; Abbott Mary-Alice; Lanpher Brendan C; Ou Zhishuo; Kang Sung-Hae L; Patel Ankita; Scaglia Fernando; Lupski James R; Cheung Sau Wai; Stankiewicz Pawel
Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping.
Human genetics 2009;126(4):589-602.
2009: Shinawi Marwan; Patel Ankita; Panichkul Prisana; Zascavage Roxanne; Peters Sarika U; Scaglia Fernando
The Xp contiguous deletion syndrome and autism.
American journal of medical genetics. Part A 2009;149A(6):1138-48.
2009: Ben-Shachar S; Lanpher B; German J R; Qasaymeh M; Potocki L; Nagamani S C Sreenath; Franco L M; Malphrus A; Bottenfield G W; Spence J E; Amato S; Rousseau J A; Moghaddam B; Skinner C; Skinner S A; Bernes S; Armstrong N; Shinawi M; Stankiewicz P; Patel A; Cheung S-W; Lupski J R; Beaudet A L; Sahoo T
Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders.
Journal of medical genetics 2009;46(6):382-8.
2009: Dhar Shweta U; Robbins-Furman Patricia; Levy Moise L; Patel Ankita; Scaglia Fernando
Tetrasomy 13q mosaicism associated with phylloid hypomelanosis and precocious puberty.
American journal of medical genetics. Part A 2009;149A(5):993-6.
2009: Yatsenko Svetlana A; Shaw Chad A; Ou Zhishuo; Pursley Amber N; Patel Ankita; Bi Weimin; Cheung Sau Wai; Lupski James R; Chinault A Craig; Beaudet Arthur L
Microarray-based comparative genomic hybridization using sex-matched reference DNA provides greater sensitivity for detection of sex chromosome imbalances than array-comparative genomic hybridization with sex-mismatched reference DNA.
The Journal of molecular diagnostics : JMD 2009;11(3):226-37.
2009: Nagamani Sandesh Chakravarthy Sreenath; Erez Ayelet; Eng Christine; Ou Zhishuo; Chinault Craig; Workman Laura; Coldwell James; Stankiewicz Pawel; Patel Ankita; Lupski James R; Cheung Sau Wai
Interstitial deletion of 6q25.2-q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss.
European journal of human genetics : EJHG 2009;17(5):573-81.
2009: Van den Veyver Ignatia B; Patel Ankita; Shaw Chad A; Pursley Amber N; Kang Sung-Hae L; Simovich Marcia J; Ward Patricia A; Darilek Sandra; Johnson Anthony; Neill Sarah E; Bi Weimin; White Lisa D; Eng Christine M; Lupski James R; Cheung Sau Wai; Beaudet Arthur L
Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.
Prenatal diagnosis 2009;29(1):29-39.
2008: Lu Xin-Yan; Phung Mai T; Shaw Chad A; Pham Kim; Neil Sarah E; Patel Ankita; Sahoo Trilochan; Bacino Carlos A; Stankiewicz Pawel; Kang Sung-Hae Lee; Lalani Seema; Chinault A Craig; Lupski James R; Cheung Sau W; Beaudet Arthur L
Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis.
Pediatrics 2008;122(6):1310-8.
2008: Bi Weimin; Breman Amy M; Venable Susan F; Eng Patricia A; Sahoo Trilochan; Lu Xin-Yan; Patel Ankita; Beaudet Arthur L; Cheung Sau Wai; White Lisa D
Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH.
Prenatal diagnosis 2008;28(10):943-9.
2008: Shao Lina; Shaw Chad A; Lu Xin-Yan; Sahoo Trilochan; Bacino Carlos A; Lalani Seema R; Stankiewicz Pawel; Yatsenko Svetlana A; Li Yinfeng; Neill Sarah; Pursley Amber N; Chinault A Craig; Patel Ankita; Beaudet Arthur L; Lupski James R; Cheung Sau W
Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.
American journal of medical genetics. Part A 2008;146A(17):2242-51.
2008: Patel Ankita; Kang Sung-Hae; Lennon Patrick Alan; Li Yin Feng; Rao P Nagesh; Abruzzo Lynne; Shaw Chad; Chinault Alan Craig; Cheung Sau W
Validation of a targeted DNA microarray for the clinical evaluation of recurrent abnormalities in chronic lymphocytic leukemia.
American journal of hematology 2008;83(7):540-6.
2008: Shinawi Marwan; Shao Lina; Jeng Linda Jo Bone; Shaw Chad A; Patel Ankita; Bacino Carlos; Sutton Vernon R; Belmont John; Cheung Sau Wai
Low-level mosaicism of trisomy 14: phenotypic and molecular characterization.
American journal of medical genetics. Part A 2008;146A(11):1395-405.
2008: Ou Zhishuo; Kang Sung-Hae L; Shaw Chad A; Carmack Condie E; White Lisa D; Patel Ankita; Beaudet Arthur L; Cheung Sau Wai; Chinault A Craig
Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses.
Genetics in medicine : official journal of the American College of Medical Genetics 2008;10(4):278-89.
2008: Ou Zhishuo; Berg Jonathan S; Yonath Hagith; Enciso Victoria B; Miller David T; Picker Jonathan; Lenzi Tiffanee; Keegan Catherine E; Sutton Vernon R; Belmont John; Chinault A Craig; Lupski James R; Cheung Sau Wai; Roeder Elizabeth; Patel Ankita
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes.
Genetics in medicine : official journal of the American College of Medical Genetics 2008;10(4):267-77.
2008: Shchelochkov Oleg A; Patel Ankita; Weissenberger George M; Chinault A Craig; Wiszniewska Joanna; Fernandes Priscilla H; Eng Christine; Kukolich Mary K; Sutton V Reid
Duplication of chromosome band 12q24.11q24.23 results in apparent Noonan syndrome.
American journal of medical genetics. Part A 2008;146A(8):1042-8.
2008: Darilek Sandra; Ward Patricia; Pursley Amber; Plunkett Katie; Furman Patti; Magoulas Pilar; Patel Ankita; Cheung Sau Wai; Eng Christine M
Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives.
Genetics in medicine : official journal of the American College of Medical Genetics 2008;10(1):13-8.
2008: Ben-Shachar Shay; Ou Zhishuo; Shaw Chad A; Belmont John W; Patel Millan S; Hummel Marybeth; Amato Stephen; Tartaglia Nicole; Berg Jonathan; Sutton V Reid; Lalani Seema R; Chinault A Craig; Cheung Sau W; Lupski James R; Patel Ankita
22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome.
American journal of human genetics 2008;82(1):214-21.
2007: Powis Zöe; Kang Sung-Hae L; Cooper M Lance; Patel Ankita; Peiffer Daniel A; Hawkins Anne; Heidenreich Randall; Gunderson Kevin L; Cheung Sau W; Erickson Robert P
Mosaic tetrasomy 12p with triplication of 12p detected by array-based comparative genomic hybridization of peripheral blood DNA.
American journal of medical genetics. Part A 2007;143A(24):2910-5.
2007: Simovich Marcia J; Yatsenko Svetlana A; Kang Sung-Hae L; Cheung Sau Wai; Dudek Martha E; Pursley Amber; Ward Patricia A; Patel Ankita; Lupski James R
Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
Prenatal diagnosis 2007;27(12):1112-7.
2007: Cheung Sau W; Shaw Chad A; Scott Daryl A; Patel Ankita; Sahoo Trilochan; Bacino Carlos A; Pursley Amber; Li Jiangzhen; Erickson Robert; Gropman Andrea L; Miller David T; Seashore Margretta R; Summers Anne M; Stankiewicz Pawel; Chinault A Craig; Lupski James R; Beaudet Arthur L; Sutton V Reid
Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics.
American journal of medical genetics. Part A 2007;143A(15):1679-86.
2007: Berg Jonathan S; Brunetti-Pierri Nicola; Peters Sarika U; Kang Sung-Hae L; Fong Chin-to; Salamone Jessica; Freedenberg Debra; Hannig Vickie L; Prock Lisa Albers; Miller David T; Raffalli Peter; Harris David J; Erickson Robert P; Cunniff Christopher; Clark Gary D; Blazo Maria A; Peiffer Daniel A; Gunderson Kevin L; Sahoo Trilochan; Patel Ankita; Lupski James R; Beaudet Arthur L; Cheung Sau Wai
Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region.
Genetics in medicine : official journal of the American College of Medical Genetics 2007;9(7):427-41.
2007: Wang Xiaoling; Reid Sutton V; Omar Peraza-Llanes J; Yu Zhiyin; Rosetta Rebecca; Kou Ying-Chuck; Eble Tanya N; Patel Ankita; Thaller Christina; Fang Ping; Van den Veyver Ignatia B
Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia.
Nature genetics 2007;39(7):836-8.
2007: Lennon P A; Cooper M L; Peiffer D A; Gunderson K L; Patel A; Peters Sarika; Cheung S W; Bacino C A
Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review.
American journal of medical genetics. Part A 2007;143A(8):791-8.
2007: Lu Xinyan; Shaw Chad A; Patel Ankita; Li Jiangzhen; Cooper M Lance; Wells William R; Sullivan Cathy M; Sahoo Trilochan; Yatsenko Svetlana A; Bacino Carlos A; Stankiewicz Pawel; Ou Zhishu; Chinault A Craig; Beaudet Arthur L; Lupski James R; Cheung Sau W; Ward Patricia A
Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases.
PloS one 2007;2(3):e327.
2006: del Gaudio Daniela; Fang Ping; Scaglia Fernando; Ward Patricia A; Craigen William J; Glaze Daniel G; Neul Jeffrey L; Patel Ankita; Lee Jennifer A; Irons Mira; Berry Susan A; Pursley Amber A; Grebe Theresa A; Freedenberg Debra; Martin Rick A; Hsich Gary E; Khera Jena R; Friedman Neil R; Zoghbi Huda Y; Eng Christine M; Lupski James R; Beaudet Arthur L; Cheung Sau Wai; Roa Benjamin B
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(12):784-92.
2006: Sahoo Trilochan; Cheung Sau Wai; Ward Patricia; Darilek Sandra; Patel Ankita; del Gaudio Daniela; Kang Sung Hae L; Lalani Seema R; Li Jiangzhen; McAdoo Sallie; Burke Audrey; Shaw Chad A; Stankiewicz Pawel; Chinault A Craig; Van den Veyver Ignatia B; Roa Benjamin B; Beaudet Arthur L; Eng Christine M
Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(11):719-27.
2006: Lennon P A; Boerkoel C F; Plunkett K; Soukam S; Cheung S W; Patel A
A novel 8.5 MB dup(1)(p34.1p34.3) characterized by FISH in a child presenting with congenital heart defect and dysmorphic features.
American journal of medical genetics. Part A 2006;140A(17):1864-70.
2006: Lennon P A; Cooper M L; Curtis M A; Lim C; Ou Z; Patel A; Cheung S W; Bacino C A
Array-based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation.
American journal of medical genetics. Part A 2006;140(11):1156-63.
2006: Lennon P A; Scott D A; Lonsdorf D; Wargowski D S; Kirkpatrick S; Patel A; Cheung S W
WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH.
American journal of medical genetics. Part A 2006;140(11):1214-8.
2005: Sheehan Andrea M; McGregor David K; Patel Ankita; Shidham Vinod; Fan Chung-Yang; Chang Chung-Che
Expression of human 8-oxoguanine DNA glycosylase (hOGG1) in follicular lymphoma.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2005;18(11):1512-8.
2005: Hwang Kwei Shuai; Pearson Margaret A; Stankiewicz Pawel; Lennon P Alan; Cooper M Lance; Wu Jessica; Ou Zhishuo; Cai Wei-Wen; Patel Ankita; Cheung Sau Wai
Cryptic unbalanced translocation t(17;18)(p13.2;q22.3) identified by subtelomeric FISH and defined by array-based comparative genomic hybridization in a patient with mental retardation and dysmorphic features.
American journal of medical genetics. Part A 2005;137(1):88-93.
2005: Cheung Sau W; Shaw Chad A; Yu Wei; Li Jiangzham; Ou Zhishuo; Patel Ankita; Yatsenko Svetlana A; Cooper Mitchell L; Furman Patti; Stankiewicz Pawel; Lupski James R; Chinault A Craig; Beaudet Arthur L
Development and validation of a CGH microarray for clinical cytogenetic diagnosis.
Genetics in medicine : official journal of the American College of Medical Genetics 2005;7(6):422-32.
2005: Scott D A; Cooper M L; Stankiewicz P; Patel A; Potocki L; Cheung S W
Congenital diaphragmatic hernia in WAGR syndrome.
American journal of medical genetics. Part A 2005;134(4):430-3.

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Ankita Patel

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